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Review

What Is the Role of Minimally Invasive Liver Surgery in Treating Patients with Hepatocellular Carcinoma on Cirrhosis?

by
Alessandro Vitale
1,†,
Roberta Angelico
2,*,†,
Bruno Sensi
2,*,
Quirino Lai
3,
Emanuele Kauffmann
4,
Irene Scalera
5,
Matteo Serenari
6,7,
Michael Ginesini
4,
Pierluigi Romano
1,
Alessandro Furlanetto
1 and
Francesco D’Amico
5 on behalf of the Italian Chapter of IHPBA (AICEP, Associazione Italiana di Chirurgia Epatobilio-Pancreatica)
1
Department of Surgical Oncological and Gastroenterological Sciences, Padua University, 35122 Padua, Italy
2
Transplant and HPB Unit, Department of Surgical Sciences, University of Rome Tor Vergata, 00133 Rome, Italy
3
General Surgery and Organ Transplantation Unit, AUO Policlinico I of Rome, Sapienza University of Rome, 00185 Rome, Italy
4
Division of General and Transplant Surgery, Pisa University, 56126 Pisa, Italy
5
Unità di Chirurgia Epatobiliare e Trapianti di Fegato, Azienda Ospedaliero—Universitaria Consorziale Policlinico di Bari, 70124 Bari, Italy
6
General Surgery and Transplant Unit, IRCCS Azienda Ospedaliero—Universitaria di Bologna, Sant’Orsola-Malpighi Hospital, 40138 Bologna, Italy
7
Department of Medical and Surgical Sciences—DIMEC, Alma Mater Studiorum—University of Bologna, 40126 Bologna, Italy
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Cancers 2024, 16(5), 966; https://doi.org/10.3390/cancers16050966
Submission received: 20 January 2024 / Revised: 24 February 2024 / Accepted: 25 February 2024 / Published: 28 February 2024
(This article belongs to the Section Methods and Technologies Development)

Abstract

:

Simple Summary

HCC is a common tumor worldwide and a major cause of tumor-related mortality. Surgical treatments are available but often impractical in severely diseased patient with cirrhosis. In the past two decades, minimally invasive liver surgery has deeply changed the HCC treatment scenario. Today, it represents a superior treatment modality compared to open surgery due to the greater compliance of cirrhotic and obese patients, the possibility of laparoscopic ablation, and possibly better oncological results.

Abstract

Minimally invasive liver surgery (MILS) has been slowly introduced in the past two decades and today represents a major weapon in the fight against HCC, for several reasons. This narrative review conveys the major emerging concepts in the field. The rise in metabolic-associated steatotic liver disease (MASLD)-related HCC means that patients with significant cardiovascular risk will benefit more profoundly from MILS. The advent of efficacious therapy is leading to conversion from non-resectable to resectable cases, and therefore more patients will be able to undergo MILS. In fact, resection outcomes with MILS are superior compared to open surgery both in the short and long term. Furthermore, indications to surgery may be further expanded by its use in Child B7 patients and by the use of laparoscopic ablation, a curative technique, instead of trans-arterial approaches in cases not amenable to radiofrequency. Therefore, in a promising new approach, multi-parametric treatment hierarchy, MILS is hierarchically superior to open surgery and comes second only to liver transplantation.

1. Introduction

Hepatocellular carcinoma (HCC) represents a major health issue worldwide as it is currently the seventh most common cancer (fifth among males and ninth among females) and the fourth cause of cancer-related death (sixth in females and second in males) [1]. Furthermore, while the highest incidence and mortality are registered in East Asian countries, its incidence is also markedly increasing in the Western world and it may soon become the third leading cause of cancer death [2,3].
HCC most often develops in the setting of chronic liver disease and especially in cirrhosis, the end-result of any chronic hepatic insult. The most commonly involved factors are hepatitis B virus (HBV), hepatitis C virus (HCV), alcohol, and metabolic-associated liver disease. They set in motion a series of events culminating in mutations in oncogenes or tumor-suppressor genes, which then promote cancer development through specific pathways (see next section).
Thus, patients with HCC often present with various clinical complexities due to the underlying liver conditions and the patient’s comorbidities which inevitably affect management [4]. In particular, the substrate of liver cirrhosis substantially limits the applicability of many of the currently used therapeutic modalities, thus significantly magnifying the complexity of treatment. In fact, given the vital role of the liver in human survival, all treatments must take into consideration post-procedural residual liver function. For example, surgical resection must leave untouched at least 25% of “normal” liver and up to 40% of cirrhotic parenchyma. This means that resection is not considerable in cases with extensive tumor burden. Furthermore, patients with severe cirrhosis (classified as Child–Pugh B or C) may not be able to tolerate resection independently from its volume, as they are poorly compliant with any perturbation to their fragile homeostasis.
Moreover, patients with metabolic-associated steatotic liver disease (MASLD) frequently suffer from multiple metabolic-related comorbidities such as ischemic heart disease, diabetes, and reduced respiratory reserve and are at higher risk of postoperative complications.
In this context, the minimization of therapeutic “invasiveness” (i.e., the impact on a patient’s delicate homeostasis) could be viewed as being of paramount importance.
Laparoscopic surgery was introduced three decades ago and has since been demonstrated to offer superior results compared to open surgery for most indications. In the setting of liver disease, its establishment has been slower due to its intrinsic difficulties, including vascular hazards, anatomical position, etc., but today it represents not only a major alternative to open surgery but probably the preferred option (Section 10).
In fact, minimally invasive liver surgery (MILS), such as laparoscopic and robotic techniques as well as image-guided ablation therapies, have emerged and established themselves as effective alternatives to traditional open surgery for patients with HCC [5,6]. As for other cancers, minimally invasive surgery has brought relevant advantages regarding early postoperative outcomes [7,8]. However, whether the minimally invasive approach determines further benefits in terms of expanding the HCC surgical indications, modifying the HCC treatment algorithm and long-term oncological outcomes, is still debated.
This narrative review aims to deeply analyze the current role of the minimally invasive liver surgical approach in treating patients with HCC on cirrhosis and its future perspectives (Figure 1).

2. Natural History of HCC

HCC has a complex pathophysiology guided by an interplay of factors including genetics, cellular microenvironment, immune cells, and interaction with risk factors such as alcohol or viruses. This translates into an intricate clinical pattern in which the history of the tumor and of the underlying predisposing disease are tightly interwoven. Next-generation sequencing has identified many oncogenic or tumor-suppressive genes which are recurrently mutated in HCC. Viral insertions, chromosome translocation, the amplification of certain genes, and the activation of telomerase are altered in 80% of HCC cases. Most commonly involved pathways are the Wnt–β-catenin (CTNNB1, AXIN1, APC), mTOR, MAPK cell cycle control (RB1, TP53, CCNE1, CCNA2, ARID1A, ARID2, PTEN, RPS6KA3, NFE2L2), oxidative stress, and epigenetic regulation [9]. As with many other cancers, in the great majority of cases, the genesis of HCC is related to chronic insults to hepatocytes, which induce concomitant liver disease and very frequently full blown cirrhosis. Thus, the predisposing factors involved are the same as those of the underlying liver affliction, such as hepatotropic viruses, alcohol, dysmetabolism, hemochromatosis, and Wilson’s disease. In fact, as we shall see, liver conditions are as important as the disease stage in directing therapeutic strategies and possibilities. Symptoms of HCC are generally absent and patients tend to manifest those related to the underlying cirrhosis including ascites and variceal hemorrhage. For this reason, in the absence of close surveillance, HCC tends to be diagnosed at an advanced stage and has historically carried very poor survival (12% five-year overall survival) [10]. On the contrary, early-stage disease tends to be relatively indolent, especially when a single nodule is present, and represents fertile ground for potentially curative treatment. Surveillance in cirrhotic patients is therefore both of paramount importance for liver disease patients’ health and cost-effective.

3. Current Management of HCC

The management of HCC remains quite unique in the oncological panorama in that it is inextricably bound and limited by the severity of liver involvement. Most specialized centers have so far based their clinical activity on the suggestions included in the BCLC (Barcelona Clinic Liver Cancer) algorithm [11]. This algorithm essentially represents a stage-based approach. In fact, it focuses on the correct staging of the disease, followed by an evaluation of liver function and performance status, and the consequent attribution to a specified treatment modality. According to BCLC, for early-stage disease, curative therapies include radiological ablation, surgical resection, and liver transplantation. All these methods have their precise indications, and their relevant limitations. For single lesions, <3 cm in diameter, radiological ablation can be considered a curative technique, while its performance is significantly limited for larger nodules. Surgical resection is more appropriate in larger nodules or multinodular disease, as it demonstrates superior oncological outcomes, yet it necessitates a sufficiently large liver remnant to avoid the risk of post-hepatectomy liver failure, a considerable limitation when considering that at least 40% of parenchyma should be spared when dealing with cirrhotic livers. Liver transplantation is known to offer the best possible long-term results as it eliminates both the current disease (HCC) and its substrate (the cirrhotic liver), decreasing the risk of post-surgical recurrence. However, the procedure is intrinsically high-risk and, more importantly, it suffers from organ shortage, and thus availability is restricted to patients who satisfy certain internationally accepted criteria. Loco-regional therapy such as trans-arterial chemo-embolization (TACE) or trans-arterial radio-embolization (TARE) are essentially considered palliative procedures to be used in intermediate stages, as evidence of the possibility of achieving cure with these techniques is currently lacking. Nonetheless, they are very useful in the context of treating patients whose disease falls outside transplant criteria, as they are often also used as complementary measures for down-staging, eventually facilitating the path to liver transplantation. Finally, systemic therapy is reserved for advanced stages and best supportive therapy for those patients whose performance status or hepatic reserve is so compromised that they are not able to tolerate systemic therapy.
While the BCLC algorithm remains an important guidance, its intrinsic rigidity has been identified as one of the main shortcomings. Despite attempts at introducing increased clinical liberty in the selection of treatment, such as the concept of “stage migration”, the system appears to remain an under-representation of contemporary treatment armamentarium. We shall see in the next paragraphs how perspectives and treatment modalities are rapidly evolving in the field.

4. Are There New Perspectives in HCC Treatment?

In recent decades, we have been observing the progressive evolution of surgical and medical treatments directed at HCC management. The major novelty has been the introduction of effective systemic therapies, particularly immunotherapy. These therapies are increasing the conversion rate from non-resectable tumors to resectable tumors [12]. Most of the available data concern the use of atezolizumab, a humanized anti-PD-L1 antibody. In one study, the atezolizumab/bevacizumab combination converted 8.6% of patients from unresectable to resectable HCC [12]. Moreover, combining systemic and loco-regional therapy may considerably further increase this rate [13]. A recent meta-analysis showed that the association between trans-arterial chemo-embolization (TACE), tyrosine-kinase inhibitors (TKIs), and immune checkpoint inhibitors (ICIs) has demonstrated the ability to convert 42% of patients from inoperable to operable disease [14]. Another effective regimen might be TACE followed by hepatic arterial infusion chemotherapy, as reported by Li et al. [15]. Moreover, in patients who successfully underwent conversion therapy, the subsequent surgical treatment appears to be associated with more prolonged survival compared to non-surgical management, albeit with possibly increased perioperative risk [16,17,18,19]. Finally, the new IMBRAVE trial has shown the effectiveness of adjuvant therapy for the first time in decreasing the risk of post-surgical tumor recurrence in high-risk HCC patients, which was confirmed in widespread reproducibility studies [20,21,22,23,24].
Thus, the answer to the first question is YES, there are new perspectives in HCC treatment, including an improved response to oncological therapy which might increase the feasibility and effectiveness of subsequent surgical therapy. This may result in an oncological push towards the expansion of MILS indications.

5. Is There a Changing Scenario in the Epidemiology of HCC?

There has been an ongoing epidemiological transition of the underlying liver-related disease leading to HCC occurrence, which might have relevant implications for HCC management.
The incidence of HCC is widely known to be correlated to the process of cirrhosis in livers with predisposing risk factors. The most commonly involved determinants are HBV, HCV, alcohol abuse, and MASLD. Worldwide, the most common etiologic factors are HBV and HCV but, especially in the Western world, this is rapidly changing due to effective anti-viral therapy and the “metabolic pandemic” that we are currently facing [9].
Nowadays, we are observing a steady decline in virus-related HCC with a concomitant rise in metabolic-associated HCC [25]. The incidence of metabolic-related HCC is increasing worldwide and currently represents the fastest growing cause of HCC, with similar reports from Europe, North America, and East Asia [25,26,27,28,29]. Patients with MASLD, especially in the presence of diabetes, may be at particular risk [30]. In Italy, this epidemiological trend has been particularly pronounced, as recently shown by Vitale A et al. [31], who demonstrated that metabolic-associated HCC is overtaking HCV-related HCC. Metabolic-associated HCC is generally more advanced, multinodular, and more often diagnosed in advanced stage than virus-related HCC [31,32,33]. Nonetheless, metabolic-associated HCC may be biologically less aggressive in terms of cancer-related death risk [31], as emerging from surgical series [34,35,36]. More importantly, metabolic-associated HCC differs from other etiologies because it might arise in a non-cirrhotic liver in as many as 20–38.5% of cases [36,37], and which patients require strict surveillance remains unclear [32]. In an effort to identify them, novel markers are being considered for HCC screening. The protein-induced by vitamin K absence (PIVKA) represents a new tool for HCC diagnosis as it carries better sensitivity than AFP [35]. Nevertheless, it still does not fulfill the criteria to be used routinely in the clinical setting, and it is suggested to be tested along with AFP. Other markers as the lens culinaris-agglutinin reactive (AFP-L3), inflammatory markers, the overexpression of oncogenes, or the downregulation of oncosuppressors and microRNA are emerging approaches, but there is still no consensus for the cut-off to be used for each marker and no competing risk analysis of them either [38]. Ongoing studies aim mainly to find a correlation between marker and early disease, to better fight the tumor. Liquid biopsy includes the analysis of circulating HCC cells and aims to perform a non-invasive sampling to predict prognosis, stage, and response to therapy, but its use in the clinical setting needs to be validated [39]. In general, the emergence of MASLD-related HCC translates into a need for revising surgical strategies. More and more HCC patients will be, on one hand, able to better tolerate more extensive hepatic resection, but on the other hand, more prone to cardiovascular morbidity. In this context, a more extensive use of the minimally invasive surgical approach for major hepatic resection or anatomical hepatic resection could thus be foreseen, aiming to minimize the physiological impact of the surgical procedure.
Therefore, the answer to the second question is YES. We are going through a new HCC epidemiology: an increase in non-early well-compensated metabolic-associated HCC. This translates in an epidemiological push toward an expansion of MILS HCC indications.

6. Does MILS Improve Post-Resection Outcomes?

The question of whether minimally invasive liver surgery (MILS) improves post-resection outcomes for HCC is a topic that has garnered considerable attention in the literature. Numerous studies provide substantial evidence supporting the significant advantages of MILS in enhancing short-term surgical outcomes for patients undergoing HCC resection when compared to the traditional open technique, particularly in high-volume centers [40,41,42,43,44,45]. Both laparoscopic and robotic techniques have demonstrated their efficacy in reducing the risk of post-hepatectomy liver failure and mitigating postoperative complications [46,47].
Nevertheless, the discussion surrounding the influence of MILS on long-term outcomes post HCC resection is characterized by nuanced debates, primarily resulting from the dearth of randomized trials and conflicting evidence among available studies. While a majority of studies report comparable outcomes between MILS and the open technique, emerging evidence suggests that the benefits of MILS may extend beyond the short term to positively impact long-term oncological endpoints [48,49]. A recent large cohort study with propensity score matching from Japan and Korea showed that laparoscopic liver resection had a better mid- and long-term disease-free survival than open hepatectomies [50]. Another multicenter study showcased a significant trend in robotic liver resection, indicating improved disease-free survival and overall survival when compared to open surgery [44]. These data have been confirmed by several updated meta-analyses [51,52,53,54,55], which conclude that MILS improves short-term and long-term oncological outcomes.
Despite the robust association between minimally invasive surgery and improved long-term outcomes, the underlying mechanisms driving this phenomenon remain elusive. One prevailing hypothesis attributes most of the benefits to the marked reduction in the risk of post-hepatectomy liver failure. Additionally, the oncological outcomes of MILS may be further optimized by conducting more frequent anatomic liver resections when feasible. This is substantiated by recent randomized clinical trials [48,56] and the escalating utilization of innovative techniques, such as indocyanine green fluorescence navigation. This navigational approach has exhibited promise in enhancing the achievement of liver resections with tumor-free margins, as evidenced by a published study indicating increased disease-free survival after MILS with indocyanine green fluorescence navigation compared to MILS without it [57]. Moreover, the expeditious recovery observed in MILS patients facilitates a quicker return to adjuvant therapy [58].
These comprehensive findings strongly suggest that MILS holds the potential not only to improve mid-term outcomes but also to exert a positive influence on long-term outcomes following liver resection. The anticipation is that further advancements will be witnessed with the widespread adoption of new technologies. Table 1 provides a meticulous summary of key studies reporting HCC oncological outcomes treated with minimally invasive surgical techniques [46,48,49,50,51,52,53,54,55].
Therefore, the answer to the third question is YES.

7. Does MILS Increase the Indications for Liver Resection?

In recent decades, an expansion of indications for liver resection in patients with HCC has been observed due to the refinements of the surgical technique [59]. In this context, several studies reported that MILS represents a favorable prognostic factor for achieving complete tumor resection (R0) [60,61]. In fact, MILS appears to be inversely correlated to the risk of postoperative liver failure and to increase the probability of achieving textbook outcomes which, in turn, improves overall survival [60,61].
Few studies have addressed specific HCC-affected populations such as cirrhotic or MASLD patients. Liver resection by minimally invasive technique was shown to decrease major morbidity and to prolong survival in patients with HCC and Child-B cirrhosis, and to reduce major postoperative complications and liver failure rates in patients with comorbid metabolic syndrome [62,63]. In both these populations, MILS was recognized as a favorable prognostic factor, although patients with Child B-7 cirrhosis may benefit more than those with Child B-8/9 cirrhosis [63,64,65,66].
Metabolic syndrome is a complex clinical entity, including hypertension, dyslipidemia, obesity, and insulin resistance. MASLD has a variable impact on liver function but is directly associated with carcinogenesis, with a significantly higher risk of developing HCC. MASLD patients have an augmented risk of morbidity and mortality after liver surgery, based on the severity of parenchymal injury and on the coexistent metabolic, vascular, and cardiological comorbidities, which strongly impact outcome. In these patients, a particular effort in mitigating the impact of complications on the postoperative course is warranted. However, despite potentially benefiting from a minimally invasive approach, obesity and comorbidities can frequently interfere with a robotic or laparoscopic approach on a technical point of view [62]. A similar concept may be proposed for elderly patients. There is wide consensus on the fact that anagraphical age is not a sufficient parameter to exclude otherwise fit patients from treatment. However, the incidence of severe comorbidities in elderly patients is significantly higher, and a thorough multi-parametric analysis of the biological age and fitness of the patient is mandatory.
From this perspective, the minimally invasive approach may compensate other adverse prognostic factors for the surgical treatment (such as Child-B cirrhosis, portal hypertension, and metabolic syndrome), and, consequently, it might expand the surgical indications in selected patients with borderline liver function or significant comorbidities [67]. Table 2 summarizes the main studies identifying MILS as a favorable prognostic factor [60,61,63,64].

8. Does MILS Expand the Indications for HCC Ablation?

The laparoscopic ablation (LA) of HCC represents another minimally invasive surgical technique that may increase the indications for surgery [68]. LA can be used when patients are unsuitable for both formal liver resection and percutaneous radiofrequency ablation (pRFA). LA permits HCC ablation without imparting an excessive insult to the hepatic parenchyma, and can provide a potentially curative alternative to TACE, which instead represents a palliative procedure. However, the lack of strong evidence on ample populations, along with technical and logistic unavailability, still strongly limits the adoption of this technique.
The laparoscopic approach to microwave ablation allows several technical issues to be overcome. The first objective advantage is the possibility to have a freer access to the liver, with several operative angles both for the ultrasound probe and for the needle. In addition, abdominal organs that might be interposed between the abdominal wall and the liver can be generally easily displaced. A second major advantage of a laparoscopic approach is the direct and effective control of any occurring bleeding by means of coagulative or surgical means. This is of paramount importance in the presence of cirrhosis-related coagulopathy, featuring both low platelet count and coagulation factor imbalance.
Recently, an Italian study reported that when textbook outcomes are reached, LA may indeed prove to be a curative therapy [69]. The same study group conducted a large multicenter study (as yet unpublished), comparing three cohorts of patients undergoing pRFA, laparoscopic microwave ablation (LA), or TACE. After weighing and balancing for heterogeneities of the three cohorts, we observed that the outcome of LA is similar to that of pRFA and superior to that of TACE.
For small nodules, even in patients with a high risk of decompensation, LA allows a radical, potentially curative approach without the incumbent risks of surgical resection.
Therefore, MILS has the potential role of increasing the span of indications to surgery as it can compensate for other adverse prognostic factors, allowing surgery in patients at higher risk of postoperative liver failure or major morbidity (i.e., cirrhosis-related portal hypertension, Child-B cirrhosis, MELD > 10, or metabolic syndrome). Moreover, LA can also allow a potentially curative surgical treatment in patients unsuitable for resection or pRFA, in whom palliative TACE is the only alternative treatment.
Therefore, the answer to this fourth question is YES.

9. Does MILS Increase the Probability of Primary or Salvage Liver Transplantation?

In selected patients with cirrhosis, liver transplantation (LT) represents the gold standard treatment for non-resectable HCC tumors [23]. The HCC selecting criteria for LT are constantly expanding [70,71], and nowadays, HCC represents the leading indication for LT [72,73]. In this scenario, MILS emerges as a transformative factor that could impact access to LT for HCC in two distinct scenarios: primary LT and salvage LT. In the first scenario, patients who are typically beyond the criteria for translatability, deemed unfit for formal resection, and with tumors in locations making radiofrequency ablation (RFA) unfeasible, find a potential solution in a minimally invasive approach with loco-regional ablation (LA). This proves to be an effective down-staging/downsizing strategy for HCC, potentially paving the way for subsequent LT. The Padua Liver Transplantation Centre’s experience attests to the success of this aggressive approach, achieving down-staging in an impressive 88% of HCC patients—a proportion significantly surpassing that observed in the XXL study, which relied solely on radiological locoregional treatments [71,74].
In the second scenario, patients who undergo primary HCC resection with an intention-to-treat curative-intent resective strategy but develop tumor recurrence can be treated by salvage transplantation if the tumor characteristics are within transplant criteria [75]. Regarding salvage LT outcomes, patients approached by MILS for the initial tumor resection seem to have benefits compared to open approaches. According to a multicenter national retrospective study conducted by Levi Sandri et al., MILS was a protective factor against the risk of LT delisting, post-transplant death, and HCC recurrence [76]. Several studies demonstrated that the beneficial effects of MILS on salvage LT outcomes may be due to lower adhesion and to easier and less hemorrhagic transplantation surgery in patients who received a previous minimally invasive liver resection compared to those treated with the open technique [76,77,78]. Moreover, a recent study has shown that the probability of receiving salvage LT is higher when resection is performed in a center with a liver transplant program [79]. All these data suggest that MILS can change the care objective from palliation to down-staging/down-sizing as a bridge to LT, thus increasing LT rates. Moreover, it facilitates the salvage LT strategy in each of its steps. A summary of the studies analyzing the effects of MILS on LT is reported in Table 3 [76,77,78]. Therefore, the answer to this fifth question is YES.
Figure 2 summarizes the overall advantages and preferred indications of MILS.

10. What Is the Role/Position of MILS in the HCC Treatment Algorithm?

In 2022, the latest version of the Barcelona Clinic Liver Cancer (BCLC) algorithm, also endorsed by the American Society for the Study of Liver Disease (AASLD), was released [11,23]. From the updated BCLC recommendations, there was an expansion of HCC indications for LT, while no advances were assigned to liver resection in the treatment algorithm. In particular, MILS has no specific role in patients with early HCC and borderline liver function, in patients with oligo-nodular or intermediate HCC (Stage B), or in patients with intrahepatic venous invasion.
Conversely, the answer to the initial question is deeply developed in a novel framework proposed in a recent policy review on HCC treatment allocation [80]. This framework has also been reproduced in Figure 1.
As discussed in a Lancet Oncology paper [80], the central limit of the BCLC system is its intrinsic “stage hierarchy” nature. Stage hierarchy means that HCC stages or sub-stages dictate treatment choice, increasing the patient’s risk of undertreatment. An exciting alternative to the stage hierarchy philosophy is the ordinal therapeutic hierarchy approach, in which treatment choice is totally or partially independent from the tumor stage, and treatment options are hierarchically ordered according to survival benefits [81,82]. However, an utterly liberal treatment hierarchy approach may increase the patient’s risk of over-treatment [81]. A solution to the limits of both stage and therapeutic hierarchy concepts is the recent proposal of a multi-parametric treatment hierarchy approach (Figure 1) [80]. In this proposal, the multi-parametric evaluation of a multidisciplinary expert team balances the ordinal therapeutic hierarchy risk of overtreating HCC patients [65].
As can be seen in the novel framework (Figure 3), MILS is hierarchically superior to open liver resection because it improves mid-term outcomes (Table 1).
Moreover, MILS can also increase the indications of liver resection since it suffers less from borderline liver function (Table 2). This aspect is also graphically underlined in the novel framework (Figure 3), where liver dysfunction has a higher probability to contraindicate open (three crosses) than minimally invasive liver resection (two crosses).
Finally, tumor ablation using LA is considered hierarchically superior to TACE, so before deciding to use intra-arterial therapy, the feasibility of LA should be considered [68,69]. This novel operative framework is fashioned to assist the decision-making of experts in the setting of a multidisciplinary meeting. The role of new systemic therapies is under scrutiny at present. However, if the auspices of a potential down-staging effect were confirmed, the scenario would become additionally complex. This “conversion-to-surgery” potential is made clear by the concept of “converse therapeutic hierarchy”, meaning that in case of a successful down-staging, previously discarded therapeutic options should be again taken into consideration, in order to offer the best possible treatment to the patient at any given time. The interesting feature of this novel operative framework relies on it being an easily adaptable tool that can be fashioned on the needs of the specific patients.

11. Conclusions

The HCC panorama is in continuous evolution. The etiology of the underlying liver disease is changing from virus- to metabolic-associated. The scientific community is devoting ample resources to developing novel therapeutic options, both in terms of systemic therapy and surgical techniques.
In this complex setting, minimally invasive liver surgery is a strong tool that has the potential to broaden the access to curative treatments (resection or ablation) to several patients, by reducing the surgical trauma and consequent impact on morbidity and mortality.
In particular, MILS offers superior short-term results compared to open surgery and appears to improve long-term survival. While more and more patients will be oncologically candidable for resection due to the reduction in tumor burden brought about by an improved response to systemic therapy, MILS will effectively expand the indications as it increases compliance to surgery, a factor of major importance especially in the setting of Child B-7 and MAFLD patients. Laparoscopic ablation should also be taken into highest consideration as a potentially curative option, hierarchically superior to TACE. Moreover, minimally invasive techniques, by having low impact and being potentially repeatable, effectively serve as down-staging procedures as a bridge to liver transplantation, and in this context, laparoscopic ablation may be superior to radiological techniques. In the context of salvage LT, MILS can decrease rates of delisting, postoperative mortality, and HCC recurrence. Overall, MILS has been established as the most important surgical tool in HCC management, second only to liver transplantation, and it must thus be considered hierarchically superior to alternative techniques such as open surgery and radiological approaches.
The management of this changing and intricate world requires an expert multidisciplinary approach and a continuous effort to interpret the wide spectrum of interplaying factors that concur in every patient reality. This personalized medicine approach reflects the need to offer the right treatment for the right patient at the right time.

Author Contributions

A.V. participated in the study design, manuscript drafting, and the critical review of the final manuscript; R.A., P.R. and A.F. participated in the writing of the manuscript; B.S. participated in the performance of the research and the writing of the manuscript; M.G.; Q.L., E.K., I.S., M.S. and F.D. participated in the study design and the critical revision of the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Cancer. IAfRo. GLOBOCAN. 2020. Available online: https://gco.iarc.fr/today/online-analysis-multi-bars?v=2020&mode=cancer&mode_population=countries&population=900&populations=900&key=asr&sex=1&cancer=39&type=0&statistic=5&prevalence=0&population_group=0&ages_group%5B%5D=0&ages_group%5B%5D=17&nb_items=10&group_cancer=1&include_nmsc=0&include_nmsc_other=1&type_multiple=%257B%2522inc%2522%253Atrue%252C%2522mort%2522%253Afalse%252C%2522prev%2522%253Afalse%257D&orientation=horizontal&type_sort=0&type_nb_items=%257B%2522top%2522%253Atrue%252C%2522bottom%2522%253Afalse%257D (accessed on 1 January 2024).
  2. McGlynn, K.A.; Petrick, J.L.; London, W.T. Global Epidemiology of Hepatocellular Carcinoma. Clin. Liver Dis. 2015, 19, 223–238. [Google Scholar] [CrossRef] [PubMed]
  3. Rahib, L.; Smith, B.D.; Aizenberg, R.; Rosenzweig, A.B.; Fleshman, J.M.; Matrisian, L.M. Projecting Cancer Incidence and Deaths to 2030: The Unexpected Burden of Thyroid, Liver, and Pancreas Cancers in the United States. Cancer Res. 2014, 74, 2913–2921. [Google Scholar] [CrossRef] [PubMed]
  4. European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. J. Hepatol. 2018, 69, 182–236. [Google Scholar] [CrossRef] [PubMed]
  5. Santambrogio, R.; Vertemati, M.; Barabino, M.; Zappa, M.A. Laparoscopic Microwave Ablation: Which Technologies Improve the Results. Cancers 2023, 15, 1814. [Google Scholar] [CrossRef] [PubMed]
  6. Zhu, P.; Liao, W.; Zhang, W.G.; Chen, L.; Shu, C.; Zhang, Z.W.; Huang, Z.Y.; Chen, Y.F.; Lau, W.Y.; Zhang, B.X.; et al. A Prospective Study Using Propensity Score Matching to Compare Long-term Survival Outcomes after Robotic-assisted, Laparoscopic, or Open Liver Resection for Patients with BCLC Stage 0-A Hepatocellular Carcinoma. Ann. Surg. 2023, 277, e103–e111. [Google Scholar] [CrossRef] [PubMed]
  7. El-Gendi, A.; El-Shafei, M.; El-Gendi, S.; Shawky, A. Laparoscopic Versus Open Hepatic Resection for Solitary Hepatocellular Carcinoma Less Than 5 cm in Cirrhotic Patients: A Randomized Controlled Study. J. Laparoendosc. Adv. Surg. Tech. A 2018, 28, 302–310. [Google Scholar] [CrossRef]
  8. Goh, B.K.P.; Syn, N.; Koh, Y.X.; Teo, J.Y.; Cheow, P.C.; Jeyaraj, P.R.; Chow, P.K.H.; Ooi, L.; Chung, A.Y.F.; Chan, C.Y. Comparison between short and long-term outcomes after minimally invasive versus open primary liver resections for hepatocellular carcinoma: A 1:1 matched analysis. J. Surg. Oncol. 2021, 124, 560–571. [Google Scholar] [CrossRef]
  9. Llovet, J.M.; Kelley, R.K.; Villanueva, A.; Singal, A.G.; Pikarsky, E.; Roayaie, S.; Lencioni, R.; Koike, K.; Zucman-Rossi, J.; Finn, R.S. Hepatocellular carcinoma. Nat. Rev. Dis. Prim. 2021, 7, 6. [Google Scholar] [CrossRef]
  10. El-Serag, H.B. Hepatocellular carcinoma. N. Engl. J. Med. 2011, 365, 1118–1127. [Google Scholar] [CrossRef]
  11. Reig, M.; Forner, A.; Rimola, J.; Ferrer-Fàbrega, J.; Burrel, M.; Garcia-Criado, Á.; Kelley, R.K.; Galle, P.R.; Mazzaferro, V.; Salem, R.; et al. BCLC strategy for prognosis prediction and treatment recommendation: The 2022 update. J. Hepatol. 2022, 76, 681–693. [Google Scholar] [CrossRef]
  12. Niizeki, T.; Tokunaga, T.; Takami, Y.; Wada, Y.; Harada, M.; Shibata, M.; Nakao, K.; Sasaki, R.; Hirai, F.; Shakado, S.; et al. Comparison of Efficacy and Safety of Atezolizumab Plus Bevacizumab and Lenvatinib as First-Line Therapy for Unresectable Hepatocellular Carcinoma: A Propensity Score Matching Analysis. Target. Oncol. 2022, 17, 643–653. [Google Scholar] [CrossRef]
  13. Pei, Y.; Li, W.; Wang, Z.; Liu, J. Successful conversion therapy for unresectable hepatocellular carcinoma is getting closer: A systematic review and meta-analysis. Front. Oncol. 2022, 12, 978823. [Google Scholar] [CrossRef]
  14. Li, W.; Pei, Y.; Wang, Z.; Liu, J. Efficacy of transarterial chemoembolization monotherapy or combination conversion therapy in unresectable hepatocellular carcinoma: A systematic review and meta-analysis. Front. Oncol. 2022, 12, 930868. [Google Scholar] [CrossRef] [PubMed]
  15. Li, B.; Qiu, J.; Zheng, Y.; Shi, Y.; Zou, R.; He, W.; Yuan, Y.; Zhang, Y.; Wang, C.; Qiu, Z.; et al. Conversion to Resectability Using Transarterial Chemoembolization Combined with Hepatic Arterial Infusion Chemotherapy for Initially Unresectable Hepatocellular Carcinoma. Ann. Surg. Open 2021, 2, e057. [Google Scholar] [CrossRef] [PubMed]
  16. Li, X.; Chen, J.; Wang, X.; Bai, T.; Lu, S.; Wei, T.; Tang, Z.; Huang, C.; Zhang, B.; Liu, B.; et al. Outcomes and prognostic factors in initially unresectable hepatocellular carcinoma treated using conversion therapy with lenvatinib and TACE plus PD-1 inhibitors. Front. Oncol. 2023, 13, 1110689. [Google Scholar] [CrossRef] [PubMed]
  17. Lin, K.-Y.; Lin, Z.-W.; Chen, Q.-J.; Luo, L.-P.; Zhang, J.-X.; Chen, J.-H.; Wang, K.; Tai, S.; Zhang, Z.-B.; Wang, S.-F.; et al. Perioperative safety, oncologic outcome, and risk factors of salvage liver resection for initially unresectable hepatocellular carcinoma converted by transarterial chemoembolization plus tyrosine kinase inhibitor and anti-PD-1 antibody: A retrospective mu. Hepatol. Int. 2023, 17, 1477–1489. [Google Scholar] [CrossRef] [PubMed]
  18. Luo, L.; He, Y.; Zhu, G.; Xiao, Y.; Song, S.; Ge, X.; Wang, T.; Xie, J.; Deng, W.; Hu, Z.; et al. Hepatectomy after Conversion Therapy for Initially Unresectable HCC: What is the Difference? J. Hepatocell. Carcinoma 2022, 9, 1353–1368. [Google Scholar] [CrossRef] [PubMed]
  19. Zhu, X.-D.; Huang, C.; Shen, Y.-H.; Xu, B.; Ge, N.-L.; Ji, Y.; Qu, X.-D.; Chen, L.; Chen, Y.; Li, M.-L.; et al. Hepatectomy after Conversion Therapy Using Tyrosine Kinase Inhibitors Plus Anti-PD-1 Antibody Therapy for Patients with Unresectable Hepatocellular Carcinoma. Ann. Surg. Oncol. 2023, 30, 2782–2790. [Google Scholar] [CrossRef] [PubMed]
  20. Cheng, A.L.; Qin, S.; Ikeda, M.; Galle, P.R.; Ducreux, M.; Kim, T.Y.; Lim, H.Y.; Kudo, M.; Breder, V.; Merle, P.; et al. Updated efficacy and safety data from IMbrave150: Atezolizumab plus bevacizumab vs. sorafenib for unresectable hepatocellular carcinoma. J. Hepatol. 2022, 76, 862–873. [Google Scholar] [CrossRef] [PubMed]
  21. Finn, R.S.; Qin, S.; Ikeda, M.; Galle, P.R.; Ducreux, M.; Kim, T.-Y.; Kudo, M.; Breder, V.; Merle, P.; Kaseb, A.O.; et al. Atezolizumab plus Bevacizumab in Unresectable Hepatocellular Carcinoma. N. Engl. J. Med. 2020, 382, 1894–1905. [Google Scholar] [CrossRef]
  22. Fulgenzi, C.A.M.; Cheon, J.; D’Alessio, A.; Nishida, N.; Ang, C.; Marron, T.U.; Wu, L.; Saeed, A.; Wietharn, B.; Cammarota, A.; et al. Reproducible safety and efficacy of atezolizumab plus bevacizumab for HCC in clinical practice: Results of the AB-real study. Eur. J. Cancer 2022, 175, 204–213. [Google Scholar] [CrossRef]
  23. Singal, A.G.; Llovet, J.M.; Yarchoan, M.; Mehta, N.; Heimbach, J.K.; Dawson, L.A.; Jou, J.H.; Kulik, L.M.; Agopian, V.G.; Marrero, J.A.; et al. AASLD Practice Guidance on prevention, diagnosis, and treatment of hepatocellular carcinoma. Hepatology 2023, 78, 1922–1965. [Google Scholar] [CrossRef]
  24. Qin, S.; Chen, M.; Cheng, A.L.; Kaseb, A.O.; Kudo, M.; Lee, H.C.; Yopp, A.C.; Zhou, J.; Wang, L.; Wen, X.; et al. Atezolizumab plus bevacizumab versus active surveillance in patients with resected or ablated high-risk hepatocellular carcinoma (IMbrave050): A randomised, open-label, multicentre, phase 3 trial. Lancet 2023, 402, 1835–1847. [Google Scholar] [CrossRef]
  25. Huang, D.Q.; Singal, A.G.; Kono, Y.; Tan, D.J.H.; El-Serag, H.B.; Loomba, R. Changing global epidemiology of liver cancer from 2010 to 2019: NASH is the fastest growing cause of liver cancer. Cell Metab. 2022, 34, 969–977.e962. [Google Scholar] [CrossRef]
  26. Mathurin, P.; de Zélicourt, M.; Laurendeau, C.; Dhaoui, M.; Kelkouli, N.; Blanc, J.F. Treatment patterns, risk factors and outcomes for patients with newly diagnosed hepatocellular carcinoma in France: A retrospective database analysis. Clin. Res. Hepatol. Gastroenterol. 2023, 47, 102124. [Google Scholar] [CrossRef] [PubMed]
  27. Myers, S.; Neyroud-Caspar, I.; Spahr, L.; Gkouvatsos, K.; Fournier, E.; Giostra, E.; Magini, G.; Frossard, J.-L.; Bascaron, M.-E.; Vernaz, N.; et al. NAFLD and MAFLD as emerging causes of HCC: A populational study. JHEP Rep. 2021, 3, 100231. [Google Scholar] [CrossRef] [PubMed]
  28. Younossi, Z.; Stepanova, M.; Ong, J.P.; Jacobson, I.M.; Bugianesi, E.; Duseja, A.; Eguchi, Y.; Wong, V.W.; Negro, F.; Yilmaz, Y.; et al. Nonalcoholic Steatohepatitis Is the Fastest Growing Cause of Hepatocellular Carcinoma in Liver Transplant Candidates. Clin. Gastroenterol. Hepatol. 2019, 17, 748–755.e743. [Google Scholar] [CrossRef] [PubMed]
  29. Zhang, C.H.; Cheng, Y.; Zhang, S.; Fan, J.; Gao, Q. Changing epidemiology of hepatocellular carcinoma in Asia. Liver Int. 2022, 42, 2029–2041. [Google Scholar] [CrossRef] [PubMed]
  30. Kim, M.N.; Han, K.; Yoo, J.; Hwang, S.G.; Zhang, X.; Ahn, S.H. Diabetic MAFLD is associated with increased risk of hepatocellular carcinoma and mortality in chronic viral hepatitis patients. Int. J. Cancer 2023, 153, 1448–1458. [Google Scholar] [CrossRef] [PubMed]
  31. Vitale, A.; Svegliati-Baroni, G.; Ortolani, A.; Cucco, M.; Dalla Riva, G.V.; Giannini, E.G.; Piscaglia, F.; Rapaccini, G.; Di Marco, M.; Caturelli, E.; et al. Epidemiological trends and trajectories of MAFLD-associated hepatocellular carcinoma 2002–2033: The ITA.LI.CA database. Gut 2023, 72, 141–152. [Google Scholar] [CrossRef] [PubMed]
  32. Piscaglia, F.; Svegliati-Baroni, G.; Barchetti, A.; Pecorelli, A.; Marinelli, S.; Tiribelli, C.; Bellentani, S. Clinical patterns of hepatocellular carcinoma in nonalcoholic fatty liver disease: A multicenter prospective study. Hepatology 2016, 63, 827–838. [Google Scholar] [CrossRef] [PubMed]
  33. Tariciotti, L.; D’Ugo, S.; Manzia, T.M.; Tognoni, V.; Sica, G.; Gentileschi, P.; Tisone, G. Combined liver transplantation and sleeve gastrectomy for end-stage liver disease in a bariatric patient: First European case-report. Int. J. Surg. Case Rep. 2016, 28, 38–41. [Google Scholar] [CrossRef]
  34. Conci, S.; Cipriani, F.; Donadon, M.; Marchitelli, I.; Ardito, F.; Famularo, S.; Perri, P.; Iaria, M.; Ansaloni, L.; Zanello, M.; et al. Hepatectomy for Metabolic Associated Fatty Liver Disease (MAFLD) related HCC: Propensity case-matched analysis with viral- and alcohol-related HCC. Eur. J. Surg. Oncol. 2022, 48, 103–112. [Google Scholar] [CrossRef]
  35. Koh, Y.X.; Tan, H.J.; Liew, Y.X.; Syn, N.; Teo, J.Y.; Lee, S.Y.; Goh, B.K.P.; Goh, G.B.B.; Chan, C.Y. Liver Resection for Nonalcoholic Fatty Liver Disease-Associated Hepatocellular Carcinoma. J. Am. Coll. Surg. 2019, 229, 467–478.e461. [Google Scholar] [CrossRef] [PubMed]
  36. Tan, D.J.H.; Ng, C.H.; Lin, S.Y.; Pan, X.H.; Tay, P.; Lim, W.H.; Teng, M.; Syn, N.; Lim, G.; Yong, J.N.; et al. Clinical characteristics, surveillance, treatment allocation, and outcomes of non-alcoholic fatty liver disease-related hepatocellular carcinoma: A systematic review and meta-analysis. Lancet Oncol. 2022, 23, 521–530. [Google Scholar] [CrossRef]
  37. Kanwal, F.; Kramer, J.R.; Mapakshi, S.; Natarajan, Y.; Chayanupatkul, M.; Richardson, P.A.; Li, L.; Desiderio, R.; Thrift, A.P.; Asch, S.M.; et al. Risk of Hepatocellular Cancer in Patients with Non-Alcoholic Fatty Liver Disease. Gastroenterology 2018, 155, 1828–1837.e1822. [Google Scholar] [CrossRef] [PubMed]
  38. Hanif, H.; Ali, M.J.; Susheela, A.T.; Khan, I.W.; Luna-Cuadros, M.A.; Khan, M.M.; Lau, D.T. Update on the applications and limitations of alpha-fetoprotein for hepatocellular carcinoma. World J. Gastroenterol. 2022, 28, 216–229. [Google Scholar] [CrossRef]
  39. Ahn, J.C.; Teng, P.C.; Chen, P.J.; Posadas, E.; Tseng, H.R.; Lu, S.C.; Yang, J.D. Detection of Circulating Tumor Cells and Their Implications as a Biomarker for Diagnosis, Prognostication, and Therapeutic Monitoring in Hepatocellular Carcinoma. Hepatology 2021, 73, 422–436. [Google Scholar] [CrossRef]
  40. Endo, Y.; Moazzam, Z.; Woldesenbet, S.; Lima, H.A.; Alaimo, L.; Munir, M.M.; Shaikh, C.F.; Yang, J.; Azap, L.; Katayama, E.; et al. Hospital Volume and Textbook Outcomes in Minimally Invasive Hepatectomy for Hepatocellular Carcinoma. J. Gastrointest. Surg. 2023, 27, 956–964. [Google Scholar] [CrossRef]
  41. Pu, J.L.; Xu, X.; Chen, L.L.; Li, C.; Jia, H.D.; Fan, Z.Q.; Li, J.D.; Guan, M.C.; Liang, Y.J.; Zhou, Y.H.; et al. Postoperative infectious complications following laparoscopic versus open hepatectomy for hepatocellular carcinoma: A multicenter propensity score analysis of 3876 patients. Int. J. Surg. 2023, 109, 2267–2275. [Google Scholar] [CrossRef]
  42. Sotiropoulos, G.C.; Prodromidou, A.; Kostakis, I.D.; Machairas, N. Meta-analysis of laparoscopic vs open liver resection for hepatocellular carcinoma. Updates Surg. 2017, 69, 291–311. [Google Scholar] [CrossRef]
  43. Wang, S.; Ye, G.; Wang, J.; Xu, S.; Ye, Q.; Ye, H. Laparoscopic versus open liver resection for hepatocellular carcinoma in elderly patients: A systematic review and meta-analysis of propensity score-matched studies. Front. Oncol. 2022, 12, 939877. [Google Scholar] [CrossRef]
  44. Giuliante, F.; Ratti, F.; Panettieri, E.; Mazzaferro, V.; Guglielmi, A.; Ettorre, G.M.; Gruttadauria, S.; Di Benedetto, F.; Cillo, U.; De Carlis, L.; et al. Short and long-term outcomes after minimally invasive liver resection for single small hepatocellular carcinoma: An analysis of 714 patients from the IGoMILS (Italian group of minimally invasive liver surgery) registry. HPB 2023, 25, 674–683. [Google Scholar] [CrossRef] [PubMed]
  45. Lippert, T.; Lim-Dy, A.; Sucandy, I. The future of minimally invasive liver resection for hepatocellular carcinoma BCLC stage 0-A. Hepatobiliary Surg. Nutr. 2023, 12, 601–603. [Google Scholar] [CrossRef] [PubMed]
  46. Di Benedetto, F.; Magistri, P.; Di Sandro, S.; Sposito, C.; Oberkofler, C.; Brandon, E.; Samstein, B.; Guidetti, C.; Papageorgiou, A.; Frassoni, S.; et al. Safety and Efficacy of Robotic vs Open Liver Resection for Hepatocellular Carcinoma. JAMA Surg. 2023, 158, 46–54. [Google Scholar] [CrossRef] [PubMed]
  47. Angelico, R.; Siragusa, L.; Serenari, M.; Scalera, I.; Kauffman, E.; Lai, Q.; Vitale, A. Rescue liver transplantation after post-hepatectomy acute liver failure: A systematic review and pooled analysis. Transplant. Rev. 2023, 37, 100773. [Google Scholar] [CrossRef] [PubMed]
  48. Kato, Y.; Sugioka, A.; Kojima, M.; Mii, S.; Uchida, Y.; Iwama, H.; Mizumoto, T.; Takahara, T.; Uyama, I. Minimally Invasive Anatomic Liver Resection for Hepatocellular Carcinoma Using the Extrahepatic Glissonian Approach: Surgical Techniques and Comparison of Outcomes with the Open Approach and between the Laparoscopic and Robotic Approaches. Cancers 2023, 15, 2219. [Google Scholar] [CrossRef] [PubMed]
  49. Cheung, T.T.; Dai, W.C.; Tsang, S.H.; Chan, A.C.; Chok, K.S.; Chan, S.C.; Lo, C.M. Pure Laparoscopic Hepatectomy Versus Open Hepatectomy for Hepatocellular Carcinoma in 110 Patients with Liver Cirrhosis: A Propensity Analysis at a Single Center. Ann. Surg. 2016, 264, 612–620. [Google Scholar] [CrossRef]
  50. Kaibori, M.; Yoshii, K.; Umeda, Y.; Yagi, T.; Okabayashi, T.; Sui, K.; Mori, A.; Hamaguchi, Y.; Kajiyama, K.; Hokuto, D.; et al. Surgical Outcomes of Laparoscopic versus Open Hepatectomy for Left Hepatocellular Carcinoma: Propensity Score Analyses Using Retrospective Japanese and Korean Individual Patient Data. Liver Cancer 2023, 12, 32–43. [Google Scholar] [CrossRef]
  51. Goh, E.L.; Chidambaram, S.; Ma, S. Laparoscopic vs open hepatectomy for hepatocellular carcinoma in patients with cirrhosis: A meta-analysis of the long-term survival outcomes. Int. J. Surg. 2018, 50, 35–42. [Google Scholar] [CrossRef]
  52. Jiang, S.; Wang, Z.; Ou, M.; Pang, Q.; Fan, D.; Cui, P. Laparoscopic Versus Open Hepatectomy in Short- and Long-Term Outcomes of the Hepatocellular Carcinoma Patients with Cirrhosis: A Systematic Review and Meta-Analysis. J. Laparoendosc. Adv. Surg. Tech. A 2019, 29, 643–654. [Google Scholar] [CrossRef] [PubMed]
  53. Kabir, T.; Tan, Z.Z.; Syn, N.L.; Wu, E.; Lin, J.D.; Zhao, J.J.; Tan, A.Y.H.; Hui, Y.; Kam, J.H.; Goh, B.K.P. Laparoscopic versus open resection of hepatocellular carcinoma in patients with cirrhosis: Meta-analysis. Br. J. Surg. 2021, 109, 21–29. [Google Scholar] [CrossRef] [PubMed]
  54. Kamarajah, S.K.; Gujjuri, R.R.; Hilal, M.A.; Manas, D.M.; White, S.A. Does minimally invasive liver resection improve long-term survival compared to open resection for hepatocellular carcinoma? A systematic review and meta-analysis. Scand. J. Surg. 2022, 111, 14574969211042455. [Google Scholar] [CrossRef] [PubMed]
  55. Pan, Y.; Xia, S.; Cai, J.; Chen, K.; Cai, X. Efficacy of Laparoscopic Hepatectomy versus Open Surgery for Hepatocellular Carcinoma with Cirrhosis: A Meta-analysis of Case-Matched Studies. Front. Oncol. 2021, 11, 652272. [Google Scholar] [CrossRef]
  56. Liao, K.; Yang, K.; Cao, L.; Lu, Y.; Zheng, B.; Li, X.; Wang, X.; Li, J.; Chen, J.; Zheng, S. Laparoscopic Anatomical Versus Non-anatomical hepatectomy in the Treatment of Hepatocellular Carcinoma: A randomised controlled trial. Int. J. Surg. 2022, 102, 106652. [Google Scholar] [CrossRef]
  57. Liu, F.; Wang, H.; Ma, W.; Li, J.; Liu, Y.; Tang, S.; Li, K.; Jiang, P.; Yang, Z.; He, Y.; et al. Short- and Long-Term Outcomes of Indocyanine Green Fluorescence Navigation- Versus Conventional-Laparoscopic Hepatectomy for Hepatocellular Carcinoma: A Propensity Score-Matched, Retrospective, Cohort Study. Ann. Surg. Oncol. 2023, 30, 1991–2002. [Google Scholar] [CrossRef]
  58. D’Hondt, M.; Tamby, E.; Boscart, I.; Turcotte, S.; Parmentier, I.; Pottel, H.; Lapointe, R.; Ovaere, S.; Vansteenkiste, F.; Vandenbroucke-Menu, F. Laparoscopic versus open parenchymal preserving liver resections in the posterosuperior segments: A case-matched study. Surg. Endosc. 2018, 32, 1478–1485. [Google Scholar] [CrossRef]
  59. Allaire, M.; Goumard, C.; Lim, C.; Le Cleach, A.; Wagner, M.; Scatton, O. New frontiers in liver resection for hepatocellular carcinoma. JHEP Rep. 2020, 2, 100134. [Google Scholar] [CrossRef]
  60. Hobeika, C.; Nault, J.C.; Barbier, L.; Schwarz, L.; Lim, C.; Laurent, A.; Gay, S.; Salamé, E.; Scatton, O.; Soubrane, O.; et al. Influence of surgical approach and quality of resection on the probability of cure for early-stage HCC occurring in cirrhosis. JHEP Rep. 2020, 2, 100153. [Google Scholar] [CrossRef]
  61. Prodeau, M.; Drumez, E.; Duhamel, A.; Vibert, E.; Farges, O.; Lassailly, G.; Mabrut, J.Y.; Hardwigsen, J.; Régimbeau, J.M.; Soubrane, O.; et al. An ordinal model to predict the risk of symptomatic liver failure in patients with cirrhosis undergoing hepatectomy. J. Hepatol. 2019, 71, 920–929. [Google Scholar] [CrossRef] [PubMed]
  62. Berardi, G.; Ivanics, T.; Sapisochin, G.; Ratti, F.; Sposito, C.; Nebbia, M.; D’Souza, D.M.; Pascual, F.; Dogeas, E.; Tohme, S.; et al. Minimally Invasive Versus Open Liver Resections for Hepatocellular Carcinoma in Patients with Metabolic Syndrome. Ann. Surg. 2023, 278, e1041–e1047. [Google Scholar] [CrossRef]
  63. Berardi, G.; Morise, Z.; Sposito, C.; Igarashi, K.; Panetta, V.; Simonelli, I.; Kim, S.; Goh, B.K.P.; Kubo, S.; Tanaka, S.; et al. Development of a nomogram to predict outcome after liver resection for hepatocellular carcinoma in Child-Pugh B cirrhosis. J. Hepatol. 2020, 72, 75–84. [Google Scholar] [CrossRef] [PubMed]
  64. Berardi, G.; Ratti, F.; Sposito, C.; Nebbia, M.; D’Souza, D.M.; Pascual, F.; Dogeas, E.; Tohme, S.; D’Amico, F.E.; Alessandris, R.; et al. Model to predict major complications following liver resection for HCC in patients with metabolic syndrome. Hepatology 2023, 77, 1527–1539. [Google Scholar] [CrossRef] [PubMed]
  65. Troisi, R.I.; Berardi, G.; Morise, Z.; Cipriani, F.; Ariizumi, S.; Sposito, C.; Panetta, V.; Simonelli, I.; Kim, S.; Goh, B.K.P.; et al. Laparoscopic and open liver resection for hepatocellular carcinoma with Child-Pugh B cirrhosis: Multicentre propensity score-matched study. Br. J. Surg. 2021, 108, 196–204. [Google Scholar] [CrossRef] [PubMed]
  66. Watanabe, Y.; Aikawa, M.; Kato, T.; Takase, K.; Watanabe, Y.; Okada, K.; Okamoto, K.; Koyama, I. Influence of Child-Pugh B7 and B8/9 cirrhosis on laparoscopic liver resection for hepatocellular carcinoma: A retrospective cohort study. Surg. Endosc. 2023, 37, 1316–1333. [Google Scholar] [CrossRef] [PubMed]
  67. Vitale, A.; Peck-Radosavljevic, M.; Giannini, E.G.; Vibert, E.; Sieghart, W.; Van Poucke, S.; Pawlik, T.M. Personalized treatment of patients with very early hepatocellular carcinoma. J. Hepatol. 2017, 66, 412–423. [Google Scholar] [CrossRef] [PubMed]
  68. Cillo, U.; Noaro, G.; Vitale, A.; Neri, D.; D’Amico, F.; Gringeri, E.; Farinati, F.; Vincenzi, V.; Vigo, M.; Zanus, G. Laparoscopic microwave ablation in patients with hepatocellular carcinoma: A prospective cohort study. HPB 2014, 16, 979–986. [Google Scholar] [CrossRef] [PubMed]
  69. Lanari, J.; Caregari, S.; Billato, I.; Gringeri, E.; D’Amico, F.; Gemo, G.; Bassi, D.; D’Amico, F.E.; Boetto, R.; Bertacco, A.; et al. Textbook Outcome of Laparoscopic Microwave Ablation for Hepatocellular Carcinoma. Cancers 2023, 15, 436. [Google Scholar] [CrossRef] [PubMed]
  70. Vitale, A.; Lai, Q. Selection of patients with hepatocellular cancer: A difficult balancing between equity, utility, and benefit. Transl. Gastroenterol. Hepatol. 2017, 2, 75. [Google Scholar] [CrossRef]
  71. Vitale, A.; Scolari, F.; Bertacco, A.; Gringeri, E.; D’Amico, F.; Bassi, D.; D’Amico, F.E.; Angeli, P.; Burra, P.; Lai, Q.; et al. Sustained Complete Response after Biological Downstaging in Patients with Hepatocellular Carcinoma: XXL-Like Prioritization for Liver Transplantation or “Wait and See” Strategy? Cancers 2021, 13, 2406. [Google Scholar] [CrossRef]
  72. Manzia, T.M.; Trapani, S.; Nardi, A.; Ricci, A.; Lenci, I.; Milana, M.; Angelico, R.; De Feo, T.M.; Agnes, S.; Andorno, E.; et al. Temporal trends of waitlistings for liver transplantation in Italy: The ECALITA (Evolution of IndiCAtion in LIver transplantation in ITAly) registry study. Dig. Liver Dis. 2022, 54, 1664–1671. [Google Scholar] [CrossRef] [PubMed]
  73. Manzia, T.M.; Angelico, R.; Toti, L.; Bellini, M.I.; Sforza, D.; Palmieri, G.; Orlando, G.; Tariciotti, L.; Angelico, M.; Tisone, G. Long-term, maintenance MMF monotherapy improves the fibrosis progression in liver transplant recipients with recurrent hepatitis C. Transpl. Int. 2011, 24, 461–468. [Google Scholar] [CrossRef]
  74. Mazzaferro, V.; Citterio, D.; Bhoori, S.; Bongini, M.; Miceli, R.; De Carlis, L.; Colledan, M.; Salizzoni, M.; Romagnoli, R.; Antonelli, B.; et al. Liver transplantation in hepatocellular carcinoma after tumour downstaging (XXL): A randomised, controlled, phase 2b/3 trial. Lancet Oncol. 2020, 21, 947–956. [Google Scholar] [CrossRef] [PubMed]
  75. Lai, Q.; Vitale, A.; Iesari, S.; Finkenstedt, A.; Mennini, G.; Spoletini, G.; Hoppe-Lotichius, M.; Vennarecci, G.; Manzia, T.M.; Nicolini, D.; et al. Intention-to-treat survival benefit of liver transplantation in patients with hepatocellular cancer. Hepatology 2017, 66, 1910–1919. [Google Scholar] [CrossRef] [PubMed]
  76. Levi Sandri, G.B.; Lai, Q.; Ravaioli, M.; Di Sandro, S.; Balzano, E.; Pagano, D.; Magistri, P.; Di Benedetto, F.; Rossi, M.; Gruttadauria, S.; et al. The Role of Salvage Transplantation in Patients Initially Treated with Open Versus Minimally Invasive Liver Surgery: An Intention-to-Treat Analysis. Liver Transpl. 2020, 26, 878–887. [Google Scholar] [CrossRef] [PubMed]
  77. Laurent, A.; Tayar, C.; Andréoletti, M.; Lauzet, J.Y.; Merle, J.C.; Cherqui, D. Laparoscopic liver resection facilitates salvage liver transplantation for hepatocellular carcinoma. J. Hepatobiliary Pancreat. Surg. 2009, 16, 310–314. [Google Scholar] [CrossRef] [PubMed]
  78. Rhu, J.; Kim, J.M.; Choi, G.S.; Kwon, C.H.D.; Joh, J.W.; Soubrane, O. Laparoscopy of hepatocellular carcinoma is helpful in minimizing intra-abdominal adhesion during salvage transplantation. Ann. Surg. Treat. Res. 2018, 95, 258–266. [Google Scholar] [CrossRef] [PubMed]
  79. Serenari, M.; Lenzi, J.; Cucchetti, A.; Cipriani, F.; Donadon, M.; Ardito, F.; Fazio, F.; Nicolini, D.; Iaria, M.; Famularo, S.; et al. The Effect of a Liver Transplant Program on the Outcomes of Resectable Hepatocellular Carcinoma: A Nationwide Multicenter Analysis. Ann. Surg. 2023, 277, 664–671. [Google Scholar] [CrossRef]
  80. Vitale, A.; Cabibbo, G.; Iavarone, M.; Viganò, L.; Pinato, D.J.; Ponziani, F.R.; Lai, Q.; Casadei-Gardini, A.; Celsa, C.; Galati, G.; et al. Personalised management of patients with hepatocellular carcinoma: A multiparametric therapeutic hierarchy concept. Lancet Oncol. 2023, 24, e312–e322. [Google Scholar] [CrossRef]
  81. Vitale, A.; Trevisani, F.; Farinati, F.; Cillo, U. Treatment of Hepatocellular Carcinoma in the Precision Medicine Era: From Treatment Stage Migration to Therapeutic Hierarchy. Hepatology 2020, 72, 2206–2218. [Google Scholar] [CrossRef]
  82. Trevisani, F.; Vitale, A.; Kudo, M.; Kulik, L.; Park, J.W.; Pinato, D.J.; Cillo, U. Merits and boundaries of the BCLC staging and treatment algorithm: Learning from the past to improve the future with a novel proposal. J. Hepatol. 2024; in press. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Review outline. Created in BioRender. HCC: hepatocellular carcinoma; MILS: minimally invasive liver surgery; LA: laparoscopic ablation; BCLC: barcelona clinic liver cancer; TACE: trans-arterial chemo-embolization.
Figure 1. Review outline. Created in BioRender. HCC: hepatocellular carcinoma; MILS: minimally invasive liver surgery; LA: laparoscopic ablation; BCLC: barcelona clinic liver cancer; TACE: trans-arterial chemo-embolization.
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Figure 2. Advantages of MILS over open surgery and TACE/RFA and preferred indications. HCC: hepatocellular carcinoma; LA: laparoscopic ablation; pRFA: percutaneous radiofrequency ablation; TACE: trans-arterial chemo-embolization.
Figure 2. Advantages of MILS over open surgery and TACE/RFA and preferred indications. HCC: hepatocellular carcinoma; LA: laparoscopic ablation; pRFA: percutaneous radiofrequency ablation; TACE: trans-arterial chemo-embolization.
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Figure 3. The novel framework includes the concepts of multi-parametric and converse therapeutic hierarchy. This figure is derived from Ref. [68]. # Performance status expresses tumor-related symptoms and, therefore, tumor aggressiveness. * Extrahepatic metastases, invasion of the main trunk of the portal vein or inferior vena cava. The right-side arrow indicates the concept of “converse therapeutic hierarchy” (conversion or adjuvant approach). The arrow is dashed and faded since the evidence supporting this concept is still weak. Abbreviations: PS, performance status; AFP, alpha-fetoprotein; PIVKA-II, Protein Induced by Vitamin-K Absence-II; LDLT, living donor liver transplantation; DCD, donor after circulatory death; MELD, model for end-stage liver disease; CRPH, clinically relevant portal hypertension; TACE, trans-arterial chemo-embolization; PVT, portal vein thrombosis. Up arrow: increased/excessive/advanced; Down arrow: insufficient.
Figure 3. The novel framework includes the concepts of multi-parametric and converse therapeutic hierarchy. This figure is derived from Ref. [68]. # Performance status expresses tumor-related symptoms and, therefore, tumor aggressiveness. * Extrahepatic metastases, invasion of the main trunk of the portal vein or inferior vena cava. The right-side arrow indicates the concept of “converse therapeutic hierarchy” (conversion or adjuvant approach). The arrow is dashed and faded since the evidence supporting this concept is still weak. Abbreviations: PS, performance status; AFP, alpha-fetoprotein; PIVKA-II, Protein Induced by Vitamin-K Absence-II; LDLT, living donor liver transplantation; DCD, donor after circulatory death; MELD, model for end-stage liver disease; CRPH, clinically relevant portal hypertension; TACE, trans-arterial chemo-embolization; PVT, portal vein thrombosis. Up arrow: increased/excessive/advanced; Down arrow: insufficient.
Cancers 16 00966 g003
Table 1. Key studies comparing outcomes of MILS vs open surgery for HCC.
Table 1. Key studies comparing outcomes of MILS vs open surgery for HCC.
YearAuthorJournalStudy TypeN° of PatientsOutcomes
2016Tan To Cheung et al. [49]Annals of SurgeryRetrospective
Propensity score matching
110 MILS
330 OPEN
-Increased 1-, 3-, and 5-year overall survival
(98.9%, 89.8%, and 83.7% in the laparoscopic group, and 94%, 79.3%, and 67.4% vin the open group)
2018Goh et al. [51]International Journal of SurgeryMeta-analysis
(five non-randomized case-matched studies)
276 MILS
612 OPEN
-Lower tumor recurrence
-Increased 1-, 3-, and 5-year overall survival
-Increased disease-free survival at 1 year
2019Jiang et al. [52]Journal of Lap and Advanced Surgical TechniquesMeta-analysis
(17 non-randomized case-matched studies)
798 MILS
1206 OPEN
-Increased 1-, 3-, and 5-year overall survival
-Increased disease-free survival at 1 year
-Decreased blood loss and transfusion rates
-Decreased postoperative complications
-Wider surgical margin
-Decreased postoperative hospital stay
-Decreased mortality
2021Pan et al. [55]Frontiers in OncologyMeta-analysis
(12 non-randomized case-matched studies)
784 MILS
1191 OPEN
-Increased 1-, 3-, and 5-year overall survival
-Decreased overall and major complications
-Decreased porstoperative mortality
-Decreased postoperative liver failure and ascites
2021Kabir et al. [53]British Journal of SurgeryMeta-analysis
(11 non-randomized case-matched studies)
690 MILS
928 OPEN
-A 16% reduction in the hazard ratio of death
-Decreased length of stay
-Decreased blood loss
-Decreased overall and major complications
2022Kaibori et al. [50]Liver CancerRetrospective
Propensity score analysis
146 MILS
807 OPEN
-Increased overall disease-free survival
-Increased disease-free and overall survival for sub-group of patients with single HCC or >4 cm.
-Decreased postoperative complictions
-Decreased postoperative hepatic decompensation
2022Kamarajah et al. [54]Scandinavian Journal of SurgeryMeta-analysis (50 non-randomized studies)4071 MILS
9660 OPEN
-Increased 3-year disease-specific mortality
-Increased 5-year all-cause mortality
2023Di Benedetto et al. [46]JAMA SurgRetrospective Propensity score matching106 MILS (robotic)
106 OPEN
-Decreased post-hepatectomy liver failure
-Decreased hospital stay
-Decreased admissions to intensive care
2023Kato et al. [48]CancersRetrospective Propensity score matching91 MILS
91 OPEN
-Longer overall survival and recurrence-free survival
-Decreased blood loss and transfusion rates
-Decreased 90-day morbidity and mortality
-Decreased bile leak
-Decreased postoperative hospital stay
Table 2. Main studies identifying MILS as a favorable prognostic factor.
Table 2. Main studies identifying MILS as a favorable prognostic factor.
YearAuthorJournalStudy TypeN° of PatientsResults
2019Prodeau et al. [61]Journal of HepatologyProspective observational study112 MILS
231 OPEN
MILS was independently inversely correlated to the likelihood of postoperative liver failure.
2020Hobeika et al. [60]JHEP ReportsProspective observational study267 MILS
158 OPEN
MILS was independently correlated to textbook outcomes.
2020Berardi et al. [63]Journal of HepatologyRetrospective study122 MILS
131 OPEN
MILS was independently inversely correlated to major morbidity in Child-B cirrhosis.
2023Berardi et al. [64]HepatologyRetrospective study445 MILS
642 OPEN
MILS was independently inversely correlated to major morbidity in patients with metabolic syndrome.
Table 3. Main studies on the effect of MILS on LT.
Table 3. Main studies on the effect of MILS on LT.
YearAuthorJournalStudy TypeN° of PatientsOutcomes
2009Laurent et al. [77]Journal of Hepatobiliary and Pancreatic SurgeryRetrospective monocentric study12 MILS
12 OPEN
LT after MILS was correlated to reduced operative time, blood loss, and transfusion requirements.
2018Rhu et al. [78]Annals of Surgical Treatment and ResearchRetrospective monocentric study10 MILS
52 OPEN
MILS reduced intra-abdominal adhesions during salvage LT.
2020Levi Sandri et al. [76]Liver TransplantationRetrospective multicentric study44 MILS
167 OPEN
MILS was independently correlated to a reduced risk of delisting, post-transplant death, and HCC recurrence.
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Vitale, A.; Angelico, R.; Sensi, B.; Lai, Q.; Kauffmann, E.; Scalera, I.; Serenari, M.; Ginesini, M.; Romano, P.; Furlanetto, A.; et al. What Is the Role of Minimally Invasive Liver Surgery in Treating Patients with Hepatocellular Carcinoma on Cirrhosis? Cancers 2024, 16, 966. https://doi.org/10.3390/cancers16050966

AMA Style

Vitale A, Angelico R, Sensi B, Lai Q, Kauffmann E, Scalera I, Serenari M, Ginesini M, Romano P, Furlanetto A, et al. What Is the Role of Minimally Invasive Liver Surgery in Treating Patients with Hepatocellular Carcinoma on Cirrhosis? Cancers. 2024; 16(5):966. https://doi.org/10.3390/cancers16050966

Chicago/Turabian Style

Vitale, Alessandro, Roberta Angelico, Bruno Sensi, Quirino Lai, Emanuele Kauffmann, Irene Scalera, Matteo Serenari, Michael Ginesini, Pierluigi Romano, Alessandro Furlanetto, and et al. 2024. "What Is the Role of Minimally Invasive Liver Surgery in Treating Patients with Hepatocellular Carcinoma on Cirrhosis?" Cancers 16, no. 5: 966. https://doi.org/10.3390/cancers16050966

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