1. Introduction
Radioembolization with yttrium-90 (
90Y)-loaded resin microspheres (RE, or selective internal radiation therapy [SIRT]) has emerged as an alternative treatment option for patients with primary and secondary liver cancer. However, RE has failed to prove survival benefit in randomized trials, and, depending on various factors including tumor biology, response rates may vary considerably [
1,
2,
3,
4,
5]. A post hoc analysis of the SARAH trial as well as a competing prospective phase II cohort from another group demonstrated positive correlations between survival and absorbed tumor dose in HCC [
6,
7]. Recently published smaller single center studies corroborated these observations in metastatic breast and colorectal cancer [
8,
9,
10]. Therefore, increasing currently prescribed tumor doses may often be favorable for improving patient outcomes [
11].
Dominant limiting factor for increasing RE dose prescriptions is the relatively low tolerance of liver parenchyma to radiation, which can lead to a deterioration in liver function and even hepatic failure, typically 2 weeks to 4 months after RE [
12]. This syndrome is known as radioembolization- or radiation-induced liver disease (RILD). It is characterized by jaundice, development of, or increase in, ascites, hyperbilirubinemia, and hypoalbuminemia in the absence of tumor progression or biliary obstruction [
13]. The pathological correlate of radiation-induced liver damage is veno-occlusive disease (VOD). VOD represents an early reaction after radiation exposure and has first been described in patients undergoing external beam radiation therapy. In brief, radiation induced endothelial cell damage followed by inflammation triggers local thrombosis, leading to microvascular flow insufficiency (“sinusoidal congestion”), release of cytotoxic substances and finally hepatocellular necrosis [
14,
15,
16,
17]. Preventive drug regimen directed against RILD could mitigate radiation damage and serve developing dose modifications but are still the subject of ongoing research. The current recommendation for RILD prevention after RE is a combination of UCDA and cortisone based on previous work by Gil-Alzugaray et al. [
18,
19]. One limitation of that regimen is that a considerable number of patients, especially the elderly and diabetic patients, do not tolerate cortisone treatment and discontinue prematurely due to the development of blood sugar changes. In addition, the pathophysiological mechanism behind RILD with VOD does not clearly support the use of cortisone in the acute phase, but rather in the chronic phase to modulate inflammatory mechanisms. A prospective study demonstrated significant mitigation of early focal radiation induced liver injury (fRILI) by post-therapeutic administration of pentoxifylline (PTX), ursodeoxycholic acid (UDCA) and low-molecular weight heparin (LMWH) in patients who underwent image-guided high-dose-rate interstitial brachytherapy of liver metastases [
20]. The underlying rationale behind this drug combination is to target acute sinusoidal congestion after radiation by adding an anticoagulant (LMWH) as well as a rheological agent (PTX) to UCDA. UDCA reduces the concentration of potentially hepatotoxic bile acids and presumably downregulates proinflammatory cytokines such as tumor-necrosis factor α (TNF-α) and interleukin-1 [
21,
22].
This study was limited by employing hepatobiliary MRI as a surrogate for focal liver dysfunction after radiation. However, this surrogate has been verified by histopathological proof [
23]. Studies have shown that diffuse metastatic disease and prior exposure to chemotherapy increase the risk of RILD [
12,
18,
24,
25,
26,
27]. In liver metastatic breast cancer (LMBC), the degree of liver involvement and liver dysfunction adversely affects patient survival, and LMBC patients that receive RE have generally undergone multiple previous chemotherapies, which makes them a particular risk group to develop RILD after RE [
28,
29,
30,
31,
32,
33]. To determine the efficacy of post-therapeutic RILD prophylaxis with PTX, UDCA and LMWH (modified prophylaxis; MP), we selected a group of intensely pretreated LMBC patients who had received RE during their treatment course. We compared an early cohort undergoing standard prevention including cortisone treatment (standard prophylaxis; SP), and a later group receiving the modified scheme with PTX, UDCA and LMWH (MP). The aim of the study was to see if the different drug regimens have an impact on post-RE liver toxicity and to see if there is a difference in RILD-occurrence.
2. Materials and Methods
2.1. Study Design and Population
This was a retrospective analysis of prospectively collected data of patients with LMBC treated with RE at a single center between June 2007 and August 2016. The study which was conducted according to the Helsinki Declaration of 2013 was approved by the local ethics committee (Ethics commission University of Magdeburg: reg. no. IRB00006099, Office for Human Research Protections, Rockville, MD, USA). Written informed consent was waived due to the retrospective nature.
The decision for RE was taken by a multidisciplinary team. Selection of patients for RE was based on the presence of unresectable hepatic metastases and lack of acceptable chemotherapeutic options (progression after standard chemotherapeutic protocols, therapy discontinuation due to toxicity, patient refusal or for consolidation treatment). Patients had liver-predominant disease, preserved liver function and an acceptable performance status (Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2). Patients with a miliary liver disease pattern were excluded.
2.2. Radioembolization
RE, including pre-procedural diagnostic work-up, was performed according to a standard algorithm as described previously using
90Y resin microspheres (SIR-Spheres
®, Sirtex Medical, Woburn, MA, USA) [
34]. This work-up included
99mTc macroaggregated albumin (
99mTc-MAA) planar imaging to estimate the lung shunt fraction and SPECT CT imaging to exclude extrahepatic accumulations. The activity of the
90Y resin microspheres was calculated by the body surface area (BSA) method. Depending on tumor distribution,
90Y resin microspheres were delivered selectively into the hepatic arteries (using a transfemoral approach) in a single session (unilobar or bilobar) or in two sessions as sequential treatment of each lobe 4–8 weeks apart (sequential bilobar).
2.3. RILD Prophylaxis
Between June 2007 and January 2014 all patients undergoing RE received SP consisting of UDCA (oral 500 mg daily; Ursofalk, Falk Pharma, Freiburg, Germany) and prednisolone (oral 5 mg daily) from the day after RE for 8 weeks [
18,
35,
36]. Following the publication of data on the prophylaxis of RILD, the protocol was modified in January 2014. Subsequently, all patients received post-therapeutic modified prophylaxis (MP) with PTX (oral 400 mg three times daily; Trental, Sanofi Aventis, Paris, France), UDCA (oral 250 mg three times a daily) and low-dose LMWH (subcutaneous injection of 40 mg daily (4000 IU); Clexane, Sanofi Aventis, Paris, France) for 8 weeks [
20].
2.4. Imaging and Volumetry
Baseline iodine contrast agent (90 mL Imeron 300, Iomeprol, Bracco, Princeton, NJ, USA) computed tomography (CT) of the thorax and abdomen (multislice CT, either 16 (Toshiba Aquilion, Toshiba Medical, Tokyo, Japan) or 64 (Siemens Definition AS, Erlangen, Germany) row detector system) and gadolinium ethoxybenzyl diethylenetriamine pentaacetic acid (Gd-EOB-DTPA; Primovist, Bayer Healthcare, Leverkusen, Germany; 0.025 mmol/kg/bodyweight) enhanced magnetic resonance imaging (MRI) of the liver (1.5 Tesla system, Achieva 1.5 T, Philipps, Best, the Netherlands) were available for all patients. Baseline MRI (hepatobiliary phase T1-weighted imaging, 5 mm slice thickness) was used for measurement of the tumor diameters as well as for volumetry of the liver and tumor, using the image processing software Osirix (Antoine Rosset, 2003–2011). Follow-up imaging consisted of either CT of the abdomen (with or without the thorax) or MRI of the liver every 2–4 months. Patients scheduled for sequential bilobar RE underwent MRI on the day of admission for the second RE session.
2.5. Toxicity Analysis
Partition model was used for calculation of parenchyma (healthy) liver dose during RE procedure. Routine follow up after RE included standard clinical and laboratory examinations at discharge and every 6 weeks. The National Cancer Institute’s Common Terminology Criteria for Adverse Events (CTCAE) Version 4.02 were used for clinical toxicity assessments. Mild RILD was defined as a bilirubin level ≥ 21 μmol/L and <30 μmol/L; and/or development of ascites. Severe RILD was defined as a bilirubin increase ≥30 μmol/L with or without ascites. Diagnosis of RILD required exclusion of obstructive jaundice and/or hepatic disease progression.
Patients scheduled for sequential bilobar RE treatment occasionally displayed extensive and large scale reduced Gd-EOB-DTPA uptake on MRI in the treated liver lobe before the second RE session, thereby indicating treatment induced subclinical lobar liver dysfunction. In these patients, treatment of the contralateral lobe was cancelled to avoid a global liver failure upon treatment continuation. Such patients were classified as having RILD despite the lack of clinical symptoms.
2.6. Response and Survival Analysis
The primary endpoint was toxicity including RILD occurrence. OS and tumor response to treatment were secondary endpoints. Tumor response was assessed by venous phase imaging and recorded according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.0. Tumor response analyses were based on the best response recorded during follow-up, with patients demonstrating either complete remission (CR), partial remission (PR), stable disease (SD) or progression (PD). OS was defined as the time from the date of first RE session until the death of the patient.
2.7. Statistical Analysis
Statistical analysis was performed using SPSS (SPSS 23, IBM, Armonk, NY, USA). Descriptive analysis of patient and therapy characteristics was performed. Fisher´s exact test was applied for categorical variables and the Mann–Whitney-U test for ordinal or continuous variables to identify between-group differences in patients receiving SP or MP. Toxicity was analyzed by Fisher´s exact test and the Wilcoxon rank-sum test, followed by binary logistic and ordinal regressions analysis to test for independent associations between parameters.
Survival was estimated according to the Kaplan–Meier method. Univariate Cox regression analysis was performed to identify potential pre- and post-therapeutic factors influencing OS. In case of interactions, either the variable with the lower p-value in univariate analysis or, if the p-value was similar, the clinically more practicable variable was chosen to create multivariate Cox models. Factors found to have an independent impact on survival in the multivariate model were used as stratifying variables in a Kaplan–Meier analysis of survival after the first RE session. The log rank test was used for survival comparison.
To minimize a potential timeline bias, each group (SP and MP group) was divided in two equal sub-groups and OS was compared. SP was divided into group 1 (GP1SP; treatment period: 13 June 2007–22 June 2010) and group 2 (GP2SP; 23 June 2010–14 January 2014), MP was divided into group 3 (GP3MP; 15 January 2014–28 April 2015) and group 4 (GP4MP; 29 April 2015–31 August 2016).
p-Values below 0.05 were considered to indicate statistical significance.
3. Results
3.1. Population and Treatment Characteristics
A total of 93 patients with LMBC received RE treatment between June 2007 and August 2016 at our institution; 59 patients received SP and 34 patients received MP. Baseline and treatment characteristics are shown in
Table 1. The two groups were balanced in terms of tumor load, liver function and previous therapies, RE procedures and the total administered activity during RE. However, mean parenchymal (healthy) liver dose was significantly higher in the MP group (40.2 Gy (12.5–83.5) vs. 47.2 Gy (17.8–86.8),
p = 0.017) (
Table 1). Of the nine patients with planned sequential therapy who discontinued treatment after the first session, treatment of the contralateral lobe was cancelled in three patients due to confluent lobar liver injury after ipsilateral RE, depicted by decreased Gd-EOB-DTPA uptake in MRI before the second treatment session. Even though none of these three patients displayed clinical symptoms, each was counted as RILD (
n = 2, 3.3% in the SP group;
n = 1, 2.9% in the MP group).
The median time to first follow-up was 7.0 (interquartile range (IQR) 6.5–8.0) weeks (IQR).
3.2. Toxicity
Baseline and follow-up laboratory parameters are shown in
Table 2 and
Supplementary Table S1. Differences between the treatment groups at baseline in bilirubin, prothrombin time and aspartate transaminase (ASAT) were within normal range and therefore considered clinically irrelevant. A significant increase in both groups in mean alkaline phosphatase (AP) and ASAT was recorded at follow-up. Alanine transaminase (ALAT) increased significantly in the SP group only. Albumin, cholinesterase, and thrombocytes showed a significant decrease at follow up in both groups. Albumin-bilirubin (ALBI) score significantly increased in both groups. ALBI grade increased in 13 (27.1%) patients in the SP group and 5 (16.7%) patients in the MP group (not significant).
Follow-up data on toxicity were available for 78 of 93 (83.9%) patients. In total, eight cases of RILD of all grades occurred: seven in the SP group, one in the MP group (
p = 0.143). The incidence of clinical adverse events after RE is shown in
Table 3. There were more cases of mild RILD or treatment discontinuations (based on MR depiction of lobar liver dysfunction after previous ipsilateral lobar RE) in the SP group than in the MP group (5 vs. 1;
p = 0.397). Severe RILD occurred only in the SP group (
n = 2, 2.6% of overall patients), however, this difference did not reach statistical significance. Regression analysis showed no significant reduction of RILD in the MP group (
p = 0.145; OR 0.20; 95% CI 0.02–1.73). Only elevated baseline ASAT was a statistically significant predictor of RILD-occurrence in the multivariate regression analysis (
p = 0.011; OR 17.12; 95% CI 1.93–151.95;
Table S2). In addition to RILD, the most common clinical toxicities of any grade were nausea/vomiting (
n = 13, 16.7%) and abdominal pain (
n = 12, 15.4%). Nausea/vomiting occurred significantly more often in the MP group than the SP group (9 vs. 4;
p = 0.026). The incidence of Grade 3 clinical toxicity other than RILD was 3.8% (
n = 3). There were no Grade 4/5 clinical toxicities.
In addition, we performed an analysis of descriptors of emerging portal hypertension such as portal vein or spleen diameter changes during follow up. Whereas portal vein and spleen diameter increased in both treatment groups at follow up after 2–4 months, the difference between the MP and the SP group was not significant (
Table S3).
3.3. Response and Survival
Best imaging response during follow-up was available in 83 (89.2%) patients. Disease control (CR, PR or SD according to RECIST) was achieved in 74 patients (89.2%) and nine patients (10.8%) had PD.
Median OS (95% CI) after RE was 8.0 (6.2–9.8) months. Univariate Cox regression for OS identified presence of pre-therapeutic ascites, time from initial diagnosis (ID) of breast cancer to ID of metastatic liver disease, baseline bilirubin, cholinesterase, albumin, CRP, gamma-glutamyltransferase, glutamate dehydrogenase, AP, ASAT, ALAT and MP as factors with a significant impact on survival (
Table 4). In multivariate Cox models (after exclusion of interaction), MP (
p = 0.033; HR 0.47; 95% CI 0.23–0.94) and pre-therapeutic AP ≥ 2 µmol/s.L (
p = 0.013; HR 2.01; 95% CI 1.16–3.47) showed a significant impact on OS (
Table 4). Corresponding Kaplan–Meier survival curves are shown in
Supplementary Figures S1 and S2.
To exclude timeline bias, we introduced 2 cohorts for each prophylaxis group (GP1SP, and GP2SP, SP; and GP3MP and GP4MP, MP). GP3MP showed significantly better survival than GP2SP with a median OS (95% CI) of 17.0 (8.55–25.45) months versus 7.0 (5.94–8.06) months (
Table 5). Corresponding Kaplan–Meier survival curves are shown in
Supplementary Material Figure S3. There was no difference in OS between the subgroups within either prophylaxis group (GP1SP vs. GP2SP and GP3MP vs. GP4MP, respectively).
4. Discussion
The applied tumor dose is decisive for patient outcomes in RE. Previous studies have demonstrated the correlation of survival and absorbed tumor dose [
6,
7,
8,
9,
10]. In addition, variations in response rates after RE indicate a medical need for optimizing dose prescriptions [
11]. Preferably, an increase in dose should come with no change of the current safety profile regarding liver failure through RILD, as recent study outcomes of RE, e.g., in HCC, indicate that liver toxicity remains a significant adverse factor negatively influencing patient outcomes [
4,
10]. Previous reports have defined risk groups for RILD after RE also in non-cirrhotic patients suffering from metastatic disease [
12,
37,
38].
In our retrospective study we sought to determine whether a combination of pentoxifylline (PTX), ursodeoxycholic acid (UCDA) and low-molecular weight heparin (LMWH) positively affects the development of RILD after RE as compared to standard prophylaxis employing cortisone. We employed two cohorts of liver metastatic breast cancer patients who had received either standard prophylaxis with UCDA and cortisone or the modified scheme. Even though the incidence of clinical RILD events most likely was too low to generate a statistical signal, multivariate analyses identified IP an independent variable for improved survival. Furthermore, several factors lead us to hypothesize modified prophylaxis may have been at least as or slightly more effective than standard prophylaxis in preventing liver damage after RE. First, even though both treatment groups appeared to be homogenous, dose exposure of normal liver parenchyma was higher in the modified versus the standard prophylaxis group. Second, the low incidence of events adversely affected statistical proof, despite a relatively higher number of events in the SP group attributable to RILD (such as all grade RILD or ALBI grade increase). The observed survival benefit of patients on modified prophylaxis must be interpreted with caution. Even though both multivariate cox regression as well as Kaplan–Meier curves suggested a robust result, we are unable to explain this outcome. Survival data may have been confounded by unequal distribution of unidentified factors influencing long-term survival in a challenging entity such as metastatic breast cancer.
Our current data complement results from a previous study, where we were able to show that post-therapeutic application of PTX, UDCA and LMWH for eight weeks significantly reduced the extent and incidence of focal radiation induced liver injury at six weeks after high-dose-rate interstitial brachytherapy of liver metastases [
20]. Given the hypothesis generating results of the study described herein as well as the pathophysiology of RILD (which roughly splits the event into venous-occlusive and inflammatory mechanisms), a combination of anticoagulation (such as in the modified scheme) with antiinflammation (such as in the standard prophylaxis) in our view is attractive for further investigations. Based on the low toxicity profile of the modified scheme, this drug combination could be prescribed preventively after radiation therapy (no matter in which form) for at least eight weeks to patients with increased risk of RILD if there are no contraindications. The additional administration of steroids requires individual assessment of the risk of possible side effects but could be of interest in future studies. Another drug used in RILD is defibrotide, a mixture of single-stranded oligonucleotides with a poorly understood effect mechanism. It is approved for the treatment of severe hepatic VOD in patients after bone marrow transplantation [
39]. However, this therapy has not yet been tested in patients with RILD after radiotherapy, especially as prophylaxis.
Adverse events from the MP regimen were limited to an increased incidence of nausea and/or vomiting. These symptoms most likely are attributable to PTX, with nausea and vomiting described among its most frequent adverse effects [
40]. An important observation of our study was frequent aggravation of the liver function in patients of both groups. Even though several variables remained within normal limits, significant increases of liver enzymes and alkaline phosphatase (AP) were recorded. In addition, albumin, cholinesterase, and thrombocytes showed a significant decrease at follow up. Portal vein and maximum spleen diameter increased significantly. All these variables indicate that despite of preventive measures in both groups, radioembolization adversely affects liver parenchyma and, in most cases subclinical, liver function. It is uncertain whether these effects in long-term may limit subsequent tumor therapies and therefore survival.
The study had several limitations, such as those inherent in its retrospective design and small sample size, inconsistency in data collection, and the lack of randomization that could have introduced a timeline bias. No follow-up toxicity data were available for 15 patients. In addition, there were not enough events (mild or severe RILD) to reach statistical significance. Data on the development of portal hypertension by portal vein and spleen diameter measurements were limited to a time frame of up to four months only. Previous observations suggest a possible later onset of portal hypertension in selected patients undergoing RE [
41].
Our findings may stimulate further investigations in liver protective medication not only with RE, but also in other high conformal irradiation techniques of the liver. In the last decade, the introduction of RE as well as advanced high conformal precision radiotherapy such as stereotactic body irradiation or CT-guided brachytherapy has boosted scientific and clinical interest in liver irradiation. A key driver has been that these techniques enable better targeting and sparing of healthy liver tissue, thus allowing delivery of substantial tumor doses despite the relatively low tolerance of liver parenchyma to radiation [
15,
42,
43,
44].
5. Conclusions
RE and high conformal liver irradiation techniques are limited by potential adverse RILD development. RILD prophylaxis with PTX, UDCA and LMWH appears to have an independent positive impact on OS in patients with metastatic breast cancer after RE compared to prophylaxis with UDCA and prednisolone and may reduce the frequency and severity of RILD. However, mild or severe RILD events proved rare in the overall cohort, which limits the value of the results. Both drug regimens employed for post-therapeutic RILD prophylaxis were well tolerated. Results of this study as well as pathophysiological considerations warrant further investigations of RILD prophylaxis presumably targeting combinations of anticoagulation (MP) and antiinflammation (SP). In effect, advances in RILD prevention may help increasing tolerable RE or liver irradiation doses to improve patient outcomes.
Author Contributions
Conceptualization, M.S., M.P.F., H.A. and J.R. (Jens Ricke); data curation, M.S., J.B., M.P. (Maciej Pech), M.P. (Maciej Powerski), A.W., J.R. (Johannes Rueckel), J.O. and J.R. (Jens Ricke); formal analysis, M.P.F., J.B., A.T., H.I. and J.R. (Johannes Rueckel); investigation, M.S., M.P.F., J.B., R.S., M.P. (Maciej Pech), C.H., M.P. (Maciej Powerski), R.D., A.W., J.O. and J.R. (Jens Ricke); methodology, M.P.F., H.A. and J.R. (Jens Ricke); project administration, M.S., M.P.F. and J.R. (Jens Ricke); resources, M.S.; supervision, M.S. and J.R. (Jens Ricke); validation, M.S. and M.P.F.; visualization, M.P.F.; writing—original draft, M.S., M.P.F. and J.R. (Jens Ricke).; writing—review and editing, J.B., R.S., A.T., H.I., M.P. (Maciej Pech), C.H., M.P. (Maciej Powerski), R.D., A.W., J.R. (Johannes Rueckel), J.O. and H.A. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Ethics Committee of Otto-von-Guericke Universitätsklinikum, Magdeburg, Germany (Ludwig-Maximilian-University, 39120 Madgdeburg).
Informed Consent Statement
Written informed consent was waived due to the retrospective nature.
Data Availability Statement
Anonymized study data are available from the corresponding author upon reasonable request.
Conflicts of Interest
The authors report the following conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results. Max Seidensticker declares consulting for Bayer, advisory arrangements with Bayer, Sirtex and Siemens, receiving research grants from Bayer and Sirtex, and receiving travel grants from Sirtex, BTG, Bayer, Cook, Boston Scientific and Siemens; Ricarda Seidensticker declares receiving research grants and travel grants from Sirtex; Harun Ilhan declares advisory arrangements with Bayer, and research grants from Novartis; Maciej Pech declares consulting, served on a speaker‘s bureau, and receiving travel grants from Sirtex; Holger Amthauer declares research grants, travel grants, and lecture fees from Sirtex Medical Europe; Jens Ricke declares consulting, advisory arrangements, and research grants and travel grants from Sirtex Medical, and consulting, advisory arrangements and receiving travel grants from BTG. Matthias P. Fabritius, Jannik Beller, Andrei Todica, Constanze Heinze, Maciej Powerski, Robert Damm, Alexander Weiss, Johannes Rueckel and Jazan Omari have no conflicts of interest to declare. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
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Table 1.
Baseline and treatment characteristics.
Table 1.
Baseline and treatment characteristics.
Characteristic | Standard Prophylaxis (n = 59) | Modified Prophylaxis (n = 34) | p-Value |
---|
Female sex | 59 | (100.0) | 34 | (100.0) | |
Age, years | 56.0 | (49.0–67.0) | 55.0 | (51.0–64.0) | 0.861 |
Age ≤ 60 years | 36 | (61.0) | 23 | (67.6) | 0.656 |
Primary tumor | | | | | |
Estrogen receptor positive | 46 | (79.3) | 27 | (79.4) | 1.000 |
Progesterone receptor positive | 40 | (69.0) | 21 | (61.8) | 0.501 |
Hormone receptor positive a | 48 | (81.4) | 28 | (82.4) | 1.000 |
Her2 neu positive b | 13 | (22.4) | 3 | (8.8) | 0.153 |
TNBC c | 9 | (15.3) | 5 | (14.7) | 1.000 |
Grading d | | | | | |
1 | 1 | (1.7) | 1 | (2.9) | 1.000 |
2 | 33 | (55.9) | 23 | (67.6) | 0.368 |
3 | 22 | (37.2) | 9 | (26.5) | 0.357 |
Metastatic disease | | | | | |
Time ID breast cancer to ID LMBC, years | 4.0 | (1.0–6.0) | 3.0 | (1.0–8.0) | 0.810 |
Time ID metastatic liver disease to RE, months | 19.0 | (9.0–37.0) | 15.0 | (6.0–29.0) | 0.127 |
Tumor load, % | 13.0 | (3.9–24.0) | 10.0 | (4.0–20.0) | 0.263 |
Extrahepatic metastases | 42 | (71.2) | 27 | (79.4) | 0.465 |
Previous therapies | | | | | |
Chemotherapy | 58 | (98.3) | 34 | (100.0) | 1.000 |
Number of chemotherapy lines | 3 | (2–4) | 4 | (2–5) | 0.163 |
Local therapy of liver metastases | 19 | (32.2) | 6 | (17.6) | 0.151 |
Surgery | 6 | (10.2) | 1 | (2.9) | 0.416 |
Interstitial brachytherapy | 9 | (15.3) | 4 | (11.8) | 0.762 |
Radiofrequency ablation | 2 | (3.4) | 1 | (2.9) | 1.000 |
TACE | 1 | (1.7) | 0 | (0.0) | 1.000 |
Clinical data | | | | | |
ALBI grade | | | | | |
1 | 53 | (89.8) | 31 | (91.2) | 1.000 |
2 | 6 | (10.2) | 3 | (8.8) | 1.000 |
3 | 0 | (0.0) | 0 | (0.0) | |
Total liver volume, ml | 1644 | (940–3323) | 1532 | (1060–3659) | 0.109 |
Radioembolization procedure | | | | | |
Bilobar sequential | 43 | (72.9) | 22 | (64.7) | 0.484 |
Bilobar | 2 | (3.3) | 1 | (2.9) | 1.000 |
Unilobar right | 13 | (22.0) | 10 | (29.4) | 0.461 |
Unilobar left | 0 | (0.0) | 0 | (0.0) | |
Superselective e | 1 | (1.7) | 1 | (2.9) | 1.000 |
Mean (range) administered activity first session, MBq | 1007 | (540–1900) | 1080 | (490–1990) | 0.126 |
Mean (range) administered activity second session, MBq | 666 | (250–1250) | 730 | (400–1290) | 0.565 |
Mean (range) total administered activity, MBq | 1493 | (800–2700) | 1528 | (650–1990) | 0.317 |
Mean (range) parenchymal liver dose, Gy | 40.2 | (12.5–83.5) | 47.2 | (17.8–86.8) | 0.017 |
Therapy discontinuation after first session | 6 | (10.2) | 3 | (8.8) | 1.000 |
Massive disease progression | 2 | (3.3) | 1 | (2.9) | 1.000 |
Hepatic injury (imaging based) | 2 | (3.3) | 1 | (2.9) | 1.000 |
Patient withdrew from study | 1 | (1.7) | 1 | (2.9) | 1.000 |
Technical reasons | 1 | (1.7) | 0 | (0.0) | 1.000 |
Chemotherapy during follow-up | 11 | (18.6) | 2 | (5.9) | 0.069 |
Best response f,g | | | | | |
Complete remission | 1 | (1.7) | 1 | (2.9) | 1.000 |
Partial remission | 37 | (62.7) | 22 | (64.7) | 0.621 |
Stable disease | 7 | (11.9) | 6 | (17.6) | 0.759 |
Progressive disease | 5 | (8.5) | 4 | (11.8) | 1.000 |
Lost to follow-up | 6 | (10.2) | 1 | (2.9) | 0.416 |
Variable (Normal Range) | | Standard Prophylaxis (n = 48) | Modified Prophylaxis (n = 30) | p-Value (Between Group) a | p-Value (Baseline vs. Follow-Up) b |
---|
Bilirubin (<21 µmol/L) | Baseline | 7.5 ± 2.7 | 6.5 ± 3.8 | 0.035 | |
| Follow-up | 13.3 ± 22.3 | 9.4 ± 11.3 | 0.195 | 0.121/0.031 |
| Δ | 5.7 ± 22.1 | 2.9 ± 9.9 | 0.510 | |
ALBI score | Baseline | −3.1 ± 0.3 | −3.1 ± 0.3 | 0.541 | |
| Follow-up | −2.7 ± 0.6 | −2.8 ± 0.5 | 0.251 | <0.001/0.003 |
| Δ | 0.4 ± 0.5 | 0.2 ± 0.4 | 0.144 | |
ALBI grade increase FU (n) | | 13 (27.1%) | 5 (16.7%) | 0.408 | |
Table 3.
Toxicity analysis.
Table 3.
Toxicity analysis.
Variable | Standard Prophylaxis (n = 48) | Modified Prophylaxis (n = 30) | p-Value |
---|
RILD (of all grades) | 7 | (14.6) | 1 | (3.3) | 0.143 |
Mild RILD (bilirubin ≥ 21 µmol/L or ascites) | 5 | (10.4) | 0 | (0.0) | 0.150 |
Severe RILD (bilirubin ≥ 30 µmol/L and ascites) | 2 | (4.3) | 0 | (0.0) | 0.520 |
Discontinuation of treatment due to liver injury (image based) | 0 | (0.0) | 1 | (3.3) | 0.358 |
Follow-up ascites | 8 | (16.7) | 4 | (13.3) | 0.758 |
Perihepatic amount of ascites, mm (mean, range) | 3 | (0–45) | 1 | (0–20) | 0.165 |
Requiring treatment | 3 | (6.3) | 0 | (0.0) | 0.281 |
Complications apart from RILD (CTCAE 1 + 2/3/4) | 21 (19/2/0) | | 19 (19/1/0) | | |
Abdominal pain | 8 | (16.7) | 4 | (13.3) | 0.758 |
Dyspepsia | 3 | (6.3) | 2 | (6.7) | 1.000 |
Fever | 1 | (2.1) | 0 | (0.0) | 1.000 |
Fatigue | 1 | (2.1) | 2 | (6.7) | 0.555 |
Nausea/vomiting | 4 | (8.3) | 9 | (30.0) | 0.026 |
Others a | 7 | (14.6) | 6 | (20.0) | 0.548 |
Table 4.
Univariate and multivariate Cox regression analysis for overall survival following radioembolization.
Table 4.
Univariate and multivariate Cox regression analysis for overall survival following radioembolization.
Variable | Univariate Analysis | Multivariate Analysis |
---|
p-Value | Hazard Ratio (95% CI) | p-Value | Hazard Ratio (95% CI) |
---|
Age ≤ 60 | 0.581 | 1.15 (0.70–1.91) | | |
Estrogen receptor positive | 0.839 | 1.06 (0.59–1.93) | | |
Progesterone receptor positive | 0.628 | 1.14 (0.68–1.92) | | |
Hormone receptor positive a | 0.441 | 1.29 (0.67–2.49) | | |
Her2 neu positive b | 0.278 | 1.39 (0.77–2.52) | | |
TNBC c | 0.665 | 0.86 (0.42–1.74) | | |
Grading G3 d | 0.412 | 0.82 (0.51–1.31) | | |
Time ID breast cancer to ID LMBC ≥2 years | 0.033 | 0.58 (0.35–0.96) | 0.118 | 0.66 (0.40–1.11) |
Time ID metastatic liver disease to RE ≥1 year | 0.265 | 1.35 (0.80–2.28) | | |
Tumor load ≥ 5% | 0.636 | 1.15 (0.65–2.03) | | |
Maximum diameter of liver metastases ≥3.9 cm | 0.109 | 1.51 (0.91–2.49) | | |
Pretherapeutic extrahepatic disease (EHD) | | | | |
Lung is one of the metastatic sites | 0.657 | 1.18 (0.58–2.40) | | |
Bone metastases only | 0.386 | 1.25 (0.76–2.06) | | |
EHD without bone metastases | 0.718 | 0.86 (0.39–1.91) | | |
Bone metastases plus at least one other metastatic site | 0.140 | 1.62 (0.85–3.08) | | |
Pretherapeutic ascites | 0.005 | 3.89 (1.52–9.93) | 0.118 | 2.16 (0.82–5.69) |
Pretherapeutic chemotherapy ≥ 3 lines | 0.582 | 0.87 (0.53–1.42) | | |
Presence of hepatic steatosis | 0.361 | 1.33 (0.72–2.46) | | |
High-grad hepatic steatosis | 0.460 | 1.32 (0.64–2.73) | | |
Prior local therapies of liver metastases | 0.748 | 0.91 (0.53–1.58) | | |
Surgery | 0.207 | 0.51 (0.18–1.45) | | |
Interstitial brachytherapy | 0.600 | 1.20 (0.61–2.39) | | |
Radiofrequency ablation | 0.598 | 0.73 (0.23–2.35) | | |
Bilirubin ≥ 21 µmol/L | 0.011 | 15.34 (1.85–127.38) | f | |
Cholinesterase ≤ 88 µmol/s.L | 0.056 | 2.30 (0.98–5.42) | e | |
Albumin ≤ 35 g/L | 0.001 | 18.20 (3.53–93.81) | e | |
C-reactive protein ≥ 5 mg/dL | <0.001 | 2.70 (1.59–4.60) | e | |
Gamma glutamyltransferase ≥1.19 µmol/s.L | <0.001 | 4.49 (2.48–8.14) | e | |
Glutamate dehydrogenase ≥120 µmol/s.L | 0.015 | 1.85 (1.13–3.05) | e | |
Alkaline phosphatase ≥ 2 µmol/s.L | <0.001 | 2.68 (1.59–4.52) | 0.013 | 2.01 (1.16–3.47) |
Aspartate transaminase ≥ 0.83 µmol/s.L | <0.001 | 3.25 (1.92–5.52) | e | |
Alanine transaminase ≥ 0.83 µmol/s.L | 0.007 | 2.04 (1.21–3.42) | e | |
Thrombocytes ≤ 146 Gpt/L | 0.933 | 0.95 (0.30–3.05) | | |
ALBI Grade > 1 | 0.130 | 1.80 (0.84–3.85) | | |
Bilobar RE | 0.330 | 0.76 (0.44–1.32) | | |
Unilobar RE | 0.215 | 1.42 (0.82–2.49) | | |
Total administered activity ≥ 1500 MBq | 0.339 | 0.79 (0.48–1.29) | | |
Normal liver dose ≥ 40 Gy | 0.013 | 0.53 (0.33–0.88) | | |
Chemotherapy during follow-up | 0.154 | 1.63 (0.83–3.18) | | |
Modified prophylaxis | 0.004 | 0.37 (0.19–0.73) | 0.033 | 0.47 (0.23–0.94) |
Table 5.
Overall survival depending on time-point of treatment.
Table 5.
Overall survival depending on time-point of treatment.
Prophylaxis | Treatment Period | Group Assignment | Median Overall Survival after RE a | GP1SP vs. GP2SP b | GP2SP vs. GP3MP b | GP3MP vs. GP4MP b |
---|
Standard prophylaxis (n = 59) | 13 June 2007–22 June 2010 | Group 1 (GP1SP, n = 29) | 8.00 (6.96–9.04) | | | |
23 June 2010–14 January 2014 | Group 2 (GP2SP, n = 30) | 7.00 (5.94–8.06) | p = 0.546 | | |
Modified prophylaxis (n = 34) | 15 January 2014–28 April 2015 | Group 3 (GP3MP, n = 17) | 17.00 (8.55–25.45) | | p = 0.001 | |
29 April 2015–31 August 2016 | Group 4 (GP4MP, n = 17) | Not reached | | | p = 0.252 |
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