Next Article in Journal
The Use of Gemtuzumab Ozogamicin as Salvage Therapy in Patients with Acute Myeloid Leukemia: A Monocentric Real-World Experience
Next Article in Special Issue
High-Resolution Computed Tomography as an Initial Diagnostic and Localization Tool in Patients with Cerebrospinal Fluid Rhinorrhea: A Meta-Analysis
Previous Article in Journal
Human Neutrophil α-Defensins 1–3 Are Upregulated in the Microenvironment of Fibrotic Liver
Previous Article in Special Issue
Morphopathogenesis of Adult Acquired Cholesteatoma
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Medicina
Volume 59
Issue 3
10.3390/medicina59030497
medicina-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Prognostic Utilities of Various Risk Factors for Laryngeal Squamous Cell Carcinoma: A Systematic Review and Meta-Analysis

by
Do Hyun Kim
1,
Sung Won Kim
1,
Jae Sang Han
1,
Geun-Jeon Kim
1,
Mohammed Abdullah Basurrah
2 and
Se Hwan Hwang
3,*
1
Department of Otolaryngology-Head and Neck Surgery, Seoul Saint Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea
2
Department of Surgery, College of Medicine, Taif University, Taif 21944, Saudi Arabia
3
Department of Otolaryngology-Head and Neck Surgery, Bucheon Saint Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea
*
Author to whom correspondence should be addressed.
Medicina 2023, 59(3), 497; https://doi.org/10.3390/medicina59030497
Submission received: 31 January 2023 / Revised: 10 February 2023 / Accepted: 20 February 2023 / Published: 2 March 2023
(This article belongs to the Special Issue Update on Otorhinolaryngologic Diseases)
Browse Figures
Review Reports Versions Notes

Abstract

:
Objective: To assess the prognostic utilities of various risk factors for laryngeal squamous cell carcinoma. Methods: Six databases were searched to January 2022. Hazard ratios for overall survival and disease-free survival were collected and study characteristics were recorded. The risk of bias was evaluated using the Newcastle–Ottawa scale. Results: Twenty-eight studies involving 32,128 patients were finally included. In terms of overall survival, older age, a history of alcohol consumption, a high Charlson comorbidity index score, a high TNM stage (III and IV), a high tumor stage (III and IV), nodal involvement, poor pathological differentiation, primary chemoradiotherapy and radiotherapy were associated with increased risks of death. In terms of disease-free survival, older age (≥60 years), TNM stages III and IV, tumor stages III and IV, supraglottic tumors, and nodal involvement all increased the risk of death. Conclusions: The TNM stage importantly predicts overall survival, and tumor location predicts the disease-free survival of patients with laryngeal squamous cell carcinoma. Of patients with risk factors, the Charlson comorbidity index usefully predicts overall survival.

1. Introduction

Laryngeal cancer is one of the most common cancers of the head and neck, associated with significant morbidity and mortality [1,2]. Internationally, approximately 1,700,000 cases of laryngeal squamous cell carcinoma (LSCC) are reported each year, and almost 90,000 patients die [3]. Despite significant advances in instruments such as flexible laryngoscopes, surgical methods, and chemoradiation therapy, the mortality rate remains high; the 5-year survival rate is 64% because about two-thirds of patients have advanced cancer at the time of diagnosis, rendering prognosis poor [1]. Additionally, despite improvements in treatment modalities, the American Cancer Society reported that the 5-year survival rate for patients with laryngeal cancer tends to decrease [4]. Advanced laryngeal cancer can be treated with radiation therapy alone, combination chemotherapy, or combination chemotherapy and radiation therapy with total laryngectomy [5]. Recently, it has been reported that the combination of radiation and chemotherapy provides organ preservation with equivalent survival rates compared to conventional treatment using surgical resection and adjuvant radiation therapy [6]. Treatment decisions are based on tumor staging according to guidelines such as the American Joint Committee on Cancer TNM classification for laryngeal function, the patient’s general condition, and patient and physician preference.
Patient-related factors including age, sex, smoking status, alcohol consumption, and comorbidities, as well as tumor-related factors such as TNM status, tumor location, pathological differentiation, and treatment, influence the prognosis. An understanding of prognostic risk factors would improve both treatment and survival. However, it is important to evaluate which factors are more important among various risk factors. However, such studies are insufficient [3]. Additionally, to the best of our knowledge, no meta-analysis has yet evaluated the impacts of individual risk factors (including comorbidities) on LSCC prognosis. Therefore, we meta-analyzed the effects of various risk factors on prognosis. This affords important insights that can improve treatments [2]. Through this study, it would be possible to improve the understanding of which factors among the risk factors of laryngeal cancer have a greater impact on the patient’s overall survival and disease-free survival.

2. Materials and Methods

2.1. Study Registration

We used the optimal surgical literature search method [7], and reported the results as suggested by the MOOSE (Meta-analysis of Observational Studies in Epidemiology) guideline [8]. The study protocol was prospectively registered on the Open Science Framework (https://osf.io/6zrcp/ accessed on 10 October 2022).

2.2. Literature Search

PubMed, Embase, the Web of Science, SCOPUS, Google Scholar, and the Cochrane Central Register of Controlled Trials were searched from the inception of publication of the relevant study to January 2023. The key search terms were laryngeal carcinoma, laryngeal neoplasm, larynx neoplasms, neoplasm, larynx, laryngeal cancer, risk factors, prognosis, survival, hazard ratio, overall survival (OS) rate, and disease-free survival (DFS). A librarian with more than 10 years experience searched all listed references, and the authors complemented the keyword-based searches by the combinations of all possible keywords with hand screening of references listed in the retrieved articles. Two independent reviewers with more than 5 years experience selected the studies. All references listed were also searched. Two independent reviewers selected studies on LSCC prognostic factors and survival rates via title, abstract, and text review.

2.3. Selection Criteria

The inclusion criteria were: (1) a human study; (2) exploration of the relationships between various risk factors and LSCC prognosis; and (3) survival data and prognostic information including hazard ratios (HRs) with 95% confidence intervals (CIs) in terms of OS or DFS after surgery, radiation therapy, chemotherapy, or combination therapy. The exclusion criteria were: (1) case reports, reviews, book chapters, books, editorial letters, opinion papers, or animal studies; (2) double primary cancers, metastatic cancers, or invasion of adjacent cancers (e.g., esophageal cancer); (3) any history of another head and neck cancer such as tongue or salivary gland cancer; (4) studies not in English and, (5) the lack of adequate prognostic data. A flow diagram of study selection is shown in Figure 1.

2.4. Data Curation and Methodological Assessment

Data were independently extracted in an agreed form by two reviewers [9,10,11], who also evaluated the risk of bias. Any differences of opinion were resolved in a panel discussion with a third reviewer. We collected the name of the lead author, the year of publication, the study design, patient numbers, age, sex, nationality, survival outcomes, TNM stages (the American Joint Committee on Cancer TNM system), and HRs with 95% CIs for OS and DFS [2,6,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32]. HRs and 95% CIs were assessed using the usual methods if not specifically indicated in any study [33,34]. We subjected the OSs, the HRs, and the 95% CIs to multivariate analyses [35]. Statistical significance was determined based on the p values. The methodological quality (risk of bias) of each study was assessed using the Newcastle–Ottawa scale. The scores range from 0 to 9; a score ≥ 6 indicates high quality [36]. Data reported only in graphical plots were not extracted for pooled meta-analysis unless specific numeral points were discernible or the authors of the relevant studies were able to verify the data. In the event of missing or incomplete data, attempts were made to request data directly from the authors.

2.5. Statistical Analysis and Outcome Measurements

The meta-analysis was performed using R software (the R Foundation, Vienna, Austria). Heterogeneity was assessed by employing the Q statistic. The extent of heterogeneity was measured using the I2 method. An I2 of 75 to 100% indicated high, 50 to 75% medium, and 25 to 50% low heterogeneity. An I2 value < 25% reflected non-heterogeneity. When I2 < 50%, a fixed-effects model was used; when I2 ≥ 50%, a random-effects model was applied. Subgroup analyses were performed according to the TNM stage [all stages (I–IV) or advanced stages (III–IV)]. Publication bias was assessed using the Egger linear regression test and by drawing Begg funnel plots. Sensitivity analysis was achieved by measuring how the removal of single studies modified the total effects.

3. Results

3.1. Study Selection

Twenty-eight studies involving 32,128 patients were included in total (Table 1). Search terms and queries were presented as Table S1. The risks of bias are listed in Table S2. In terms of potential publication bias, the Egger test result was significant (p > 0.05), suggesting a source of such bias that was not evident in the studies. Begg funnel plots by sex (p = 0.06637) and tumor stage (p = 0.0501) revealed no publication bias (Figure S1A,B). However, funnel plot analyses by age (p < 0.0001) and nodal involvement (p < 0.0001) suggested a source of bias (Figure S1C,D). We therefore performed the Duval and Tweedie trim-and-fill test and found no significant difference between the observed and adjusted values (age 1.2217, p < 0.0001 vs. 1.0599; p = 0.0454; nodal involvement 2.0537, p < 0.0001 vs. 1.3578; p = 0.0048). Therefore, we concluded that the studies were not biased and that the results reliably reflected the clinical features. However, given the small numbers of relevant studies (<10), we did not use the Egger linear regression test or draw Begg funnel plots for alcohol consumption, smoking status, the Charlson comorbidity index, clinical stage, pathological differentiation, or tumor subsite.

3.2. Overall Survival by Patient-, Tumor-, and Treatment-Related Factors

Patient-related factors included age (≥60 or <60 years), sex, current smoking (yes or no), current alcohol consumption (yes or no), and the Charlson comorbidity index (≥2, 1, or 0). The tumor-related factors were the TNM stage (III and IV vs. I and II); tumor stage (III and IV vs. I and II); tumor location (subglottis, supraglottis, or glottis); nodal involvement (yes or no); and the extent of pathological differentiation (poor, moderate, or high). The treatment-related factors were primary chemoradiotherapy, radiotherapy, or total laryngectomy (Table 2).
In terms of overall survival, older age (>60 years) [hazard ratio (HR) 1.1300, 95% confidence interval (CI) [1.0908; 1.1705]; p < 0.0001]; a smoking history (HR 1.2926, 95% CI (1.0999; 1.5191); p = 0.0018); a history of alcohol consumption [HR 1.1979, 95% CI (1.0696; 1.3415); p = 0.0018]; a high Charlson comorbidity index score [≥2 vs. 0; HR 1.6716, 95% CI (1.3533; 2.0647); p < 0.0001 and 1 vs. 0; HR 1.3153, 95% CI (1.2299; 1.4068); p < 0.0001]; a high TNM stage (III and IV) [HR 2.4583, 95% CI (1.8323; 3.2980); p < 0.0001); a high tumor stage (III and IV) [HR 1.5648, 95% CI (1.2363; 1.9806); p < 0.0001); nodal involvement [HR 1.9439, 95% CI (1.6235; 2.3276); p < 0.0001], poor pathological differentiation [moderate vs. high; HR 1.2820, 95% CI (1.0659; 1.5419); p < 0.0001 and poor vs. high (HR 1.6951, 95% CI [1.5394; 1.8665]; p < 0.0001); supraglottic tumor (vs. glottis tumor) (HR 1.3740, 95% CI [1.0730; 1.7594; p = 0.0118); primary chemoradiotherapy and radiotherapy (vs. primary chemoradiotherapy and total laryngectomy [HR 1.4004, 95% CI (1.1639; 1.6850); p = 0.0004); and primary radiotherapy vs. total laryngectomy [HR 1.5418, 95% CI (1.1531; 2.0616); p = 0.0035] were associated with increased risk of death (Figure 2). In terms of disease-free survival, those of older age (≥60 years), TNM stages III and IV, tumor stages III and IV, with supraglottic tumors, and nodal involvement, were at increased risk of death compared to younger patients (<60 years) [HR 1.0070, 95% CI (1.0005; 1.0136); p = 0.0359), as were those of TNM stages I and II [HR 2.3987, 95% CI (2.0956; 2.7456); p < 0.0001), those of tumor stages I and II [HR 1.8441, 95% CI (1.4507; 2.3441), p < 0.0001), patients with glottis tumors [HR 1.6371, 95% CI (1.0162; 2.6373); p < 0.0001), and those lacking nodal involvement [HR 1.6174, 95% CI (1.4560; 1.7968); p < 0.0001).

3.3. Subgroups Analysis

The prognostic values revealed significant heterogeneity because patients of different TNM stages (all stages; I–IV) or advanced stages only (III–IV) were included. Therefore, we performed subgroup analyses by the TNM stage. In terms of OS, significant heterogeneity was apparent in the outcomes by age, the Charlson comorbidity index score, the TNM stage, nodal involvement, sex, tumor location (subglottis, supraglottis, or glottis), and treatment modality (primary chemoradiotherapy, radiotherapy, or total laryngectomy). Only one study compared subgroups in terms of nodal involvement, tumor location, and treatment modality; therefore, we could not perform subgroup comparisons. The OSs of subgroups classified by age, the Charlson comorbidity index score, and sex did not differ significantly, which may mean that these factors exert similar effects regardless of TNM stage. However, tumor location (supraglottis vs. glottis) exhibited significant heterogeneity. For patients of all disease stages, subgroup analysis revealed that supraglottic lesions generally reduced survival compared to that of subjects with glottis lesions, but not in patients of advanced stage.

3.4. Sensitivity Analyses

Sensitivity analyses were performed to evaluate whether the pooled estimates of overall or disease-free survival by patient-, tumor-, and treatment-related factors were different by omitting a different study each time and repeating the meta-analyses. Finally, the results were all consistent with the above outcomes.

4. Discussion

We found that older age, a higher Charlson comorbidity index (≥1), advanced TMN stage (III and IV), advanced tumor stage, nodal involvement, pathological differentiation, primary chemoradiotherapy and radiotherapy were all associated with poorer OSs. Similarly, older age, advanced TMN stage (III and IV), advanced tumor stage, a supraglottic lesion, and nodal involvement were associated with poorer DFS. For LSCC, in common with many other tumors, tumor stage (T stage), cervical lymph node metastasis, and the clinical stage are key predictors of prognosis [19,25,28]. Additionally, we found that the T stage, lymph node metastasis, and the clinical stage significantly affected prognosis; the clinical stage exerted a greater influence on survival than did the T stage or lymph node metastasis, probably because clinical staging comprehensively reflects the tumor stage and nodal invasion and metastasis [2]. In LSCC patients, apart from the clinical stage, tumor location is significantly prognostic. A supraglottic laryngeal cancer can grow significantly before the development of symptoms. Given the abundant lymphatic drainage, nodal metastases are often present at the time of onset of such symptoms [37]. In contrast, in those with glottis cancer, lymphatic drainage around the glottis is poor, and early lymph node metastases are rare (<5% of patients). Therefore, it could be predicted that early supraglottis cancers would be associated with poorer prognoses than early glottis cancers [2]. However, many advanced glottis cancers in fact arise in the laryngeal ventricle, and easily spread to the supraglottis and paraglottic space [37]. Therefore, in our subgroup analyses, the survival rates of those with advanced glottis and supraglottis cancers were similar, but when all stages (including early stages) were included, supraglottis cancers evidenced a poorer prognosis. We also found that the tumor pathological differentiation status was prognostic, as is true of many tumors [28,29]. Progression of dedifferentiation (to moderate and poor) was associated with significantly poorer prognosis, consistent with previous reports.
The treatment modality can also significantly Impact prognosis. Several early studies reported similar survival rates when chemoradiotherapy (rather than surgery) was used to treat advanced-stage laryngeal cancer (it was sought to preserve laryngeal function) [38,39]. Therefore, after publication of these prospective randomized trials, the use of primary chemoradiation therapy for LSCC increased significantly. However, after the papers were published, clinical studies showed that primary chemoradiotherapy was in fact not as good as primary surgery [32,40,41]. Dziegielewski et al. found that the OS of patients with advanced laryngeal cancers (stages T3 and T4) increased when they were treated with concurrent surgery and radiotherapy or chemoradiotherapy, compared to radiotherapy or chemoradiotherapy alone [13]. We similarly found that primary total laryngectomy was associated with better survival than radiotherapy or chemoradiotherapy alone.
Although prognostic tumor- and treatment-related factors of LSCC patients have been studied, patient-related factors are often overlooked; they are nonetheless important. Comorbidities affect disease prognosis, treatment choices, and outcomes. The Charlson comorbidity index (developed in 1987) is today widely used to identify comorbidities and to apply weighted or pathophysiological severity ratings [39]. The index validity predicts outcomes and mortality risks, including those of head and neck cancer patients [40]. Several studies found that comorbidities significantly influenced LSCC patient survival [2,17,21,22,24]. We found that the index usefully predicted overall survival, as have previous reports [42,43]. The presence of significant comorbidities is common in head and neck cancer, with approximately 30–50% of patients having at least one comorbidity [44]. With the accumulation of evidence, management of comorbidities and chronic diseases in the survival stage of head and neck cancer management is becoming increasingly important [45]. This is reported to be due to higher non-cancer related mortality, which can affect about 10–30% of patients [44]. It is also reported that about 20–30% of patients need to modify treatment decisions due to comorbidity [46]. In this context, the Charlson comorbidity index score was shown to be the next strongest risk factor for poor overall survival following the TNM clinical stage. Age may affect LSCC prognosis. On univariate analysis, Wong et al. showed that age was not associated with poor survival in patients with newly diagnosed laryngeal cancer [16]. However, Graboyes et al. found that age was prognostic with univariate and multivariate analyses of advanced laryngeal cancer [21]. Our results are consistent with those of Graboyes et al.; the survival rate of older patients was lower than that of younger subjects. Aging is associated with decreased organ function, more comorbidities, and cognitive dysfunction that adversely affect the immune system, the responses to treatment, and prognosis [47]. In addition, older patients generally receive less intensive care than younger patients [1]; they tend to be prescribed RT or CRT more often than total laryngectomy [13]. This may reduce the DFS of older patients. Smoking and alcohol consumption were associated with poor prognosis. Toxins in tobacco smoke and alcohol metabolites impair the innate defenses, adversely modulate antigen presentation, and trigger chronic inflammation of mucosal surfaces. In the case of alcohol, it can cause gastroesophageal reflux, increasing the chance of contact between the upper aerodigestive epithelium and dietary carcinogens. This can cause transformation of epithelial lesions and tumorigenesis [48]. These materials also bind to the DNA of mucosal cells, triggering mutations and malignant transformation [29]. Infiltration of immune cells from LSCC, such as mast cells, neutrophils, and macrophages, can promote cancer development and tumor angiogenesis, and produce small molecules, including cytokines, chemokines, and growth factors, which allow tumors to avoid host immune responses [49,50]. Such genetic and molecular alterations constitute a distinct pathological entity causing poor prognosis [41]. Field cancerization may be prognostically important in such patients [41,50]. Recently, studies on the role of genetic mutations in the etiology of laryngeal cancer have also been conducted. This may lead to a better understanding of mechanisms and the discovery of effective molecular markers for the development of novel screening and treatment strategies [51]. However, more investigation is required. Through this study, we reviewed LSCC risk factors and were able to identify which factors could have a greater impact on overall survival and disease-free survival of patients. This information can be important to guide consideration of adjuvant treatment modalities and preoperative discussions about treatment goals.
Our meta-analysis had several limitations. First, as some data evidenced significant heterogeneity, we used a random-effects model to perform subgroup analyses. Second, the institutional setting and (probably) unknown factors affect the prognostic utilities of various OS and DFS risk factors for OS and DFS. Additionally, it is difficult to analyze by setting the conditions of the patients in the included individual studies in the same way. Although this is a limitation of meta-analysis, it has the advantage of generalizing the results of independent studies with differences in the experimental environment. Third, 9 of the 23 articles were from China; selection bias may be in play because regional grouping was not considered. Additionally, most patients were male, which may reflect the nature of the disease per se, but may also reflect a gender bias [3]. These observations may explain the heterogeneity of our prognostic outcomes. Fourth, any cross-sectional work may over- or under-estimate disease prevalence. Finally, we encountered methodological heterogeneity and inadequate reporting of methods. To overcome these limitations, large-scale homogenous population studies are required. Fifth, in our study, we included the only studies written in English, which could restrict the diversity of results. However, exclusion of non-English publications from systematic reviews on clinical interventions had a minimal effect on overall conclusions and could be a viable methodological shortcut [52].

5. Conclusions

This meta-analysis found that TNM stage significantly predicts overall survival and tumor location predicts disease-free survival in laryngeal squamous cell carcinoma patients. In patients with risk factors, the Charlson comorbidity index is a useful predictor of overall survival. All tumor-, treatment-, and patient-related factors affect the prognosis of LSCC patients to varying extents. Many risk factors (including comorbidities) are often overlooked during prognostic evaluation. However, they are as important as other factors.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/medicina59030497/s1, Figure S1. Begg funnel plot analyses by sex (A) and tumor stage (B). Funnel plots created after performance of the Duval and Tweedie trim-and-fill test for age (C) and nodal involvement (D). Table S1. Search terms and queries. Table S2. The methodological quality of the included studies.

Author Contributions

D.H.K., study conception and design, acquisition of data, analysis and interpretation of data, drafting the article and revisions, final approval of article; S.W.K., study conception and design, analysis and interpretation of data, drafting the article and revisions, final approval of article; J.S.H., acquisition of data, analysis and interpretation of data, drafting the article and revisions, final approval of article; G.-J.K., acquisition of data, analysis and interpretation of data, drafting the article and revisions, final approval of article; M.A.B., analysis and interpretation of data, drafting the article and revisions, final approval of article; S.H.H., study conception and design, acquisition of data, analysis and interpretation of data, drafting the article and revisions, final approval of article. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Research Foundation of Republic of Korea (NRF) (2022R1F1A1066232, 2019M3A9H2032424, 2020R1I1A1A01051844), Alchemist Project 1415180884 by Ministry of Trade, Industry & Energy (MOTIE, Republic of Korea) (20012378), and the Institute of Clinical Medicine Research of Bucheon St. Mary’s Hospital, Research Fund (2022). The sponsors had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Institutional Review Board Statement

Ethical review and approval were waived for this study due to this systematic review and meta-analysis that based exclusively on published literature.

Informed Consent Statement

Informed consents were not required because this study is based exclusively on published literature.

Data Availability Statement

The raw data of individual articles used in this meta-analysis are included in the main text or supplementary data.

Conflicts of Interest

The authors declare that there are no competing interests.

Ethics Statement

An ethics statement is not applicable because this study is based exclusively on published literature.

References

  1. Santos, A.; Santos, I.C.; Dos Reis, P.F.; Rodrigues, V.D.; Peres, W.A.F. Impact of Nutritional Status on Survival in Head and Neck Cancer Patients After Total Laryngectomy. Nutr. Cancer 2021, 74, 1252–1260. [Google Scholar] [CrossRef] [PubMed]
  2. Zhang, S.Y.; Lu, Z.M.; Luo, X.N.; Chen, L.S.; Ge, P.J.; Song, X.H.; Chen, S.H.; Wu, Y.L. Retrospective analysis of prognostic factors in 205 patients with laryngeal squamous cell carcinoma who underwent surgical treatment. PLoS ONE 2013, 8, e60157. [Google Scholar]
  3. Zhao, Y.; Qin, J.; Qiu, Z.; Guo, J.; Chang, W. Prognostic role of neutrophil-to-lymphocyte ratio to laryngeal squamous cell carcinoma: A meta-analysis. Braz J. Otorhinolaryngol. 2020, 88, 717–724. [Google Scholar] [CrossRef] [PubMed]
  4. Siegel, R.; Ma, J.; Zou, Z.; Jemal, A. Cancer statistics, 2014. CA Cancer J. Clin. 2014, 64, 9–29. [Google Scholar] [CrossRef] [Green Version]
  5. Forastiere, A.A.; Zhang, Q.; Weber, R.S.; Maor, M.H.; Goepfert, H.; Pajak, T.F.; Morrison, W.; Glisson, B.; Trotti, A.; Ridge, J.A.; et al. Long-term results of RTOG 91-11: A comparison of three nonsurgical treatment strategies to preserve the larynx in patients with locally advanced larynx cancer. J. Clin. Oncol. 2013, 31, 845–852. [Google Scholar] [CrossRef]
  6. Boukovalas, S.; Goepfert, R.P.; Smith, J.M.; Mecham, E.; Liu, J.; Zafereo, M.E.; Chang, E.I.; Hessel, A.C.; Hanasono, M.M.; Gross, N.D.; et al. Association between postoperative complications and long-term oncologic outcomes following total laryngectomy: 10-year experience at MD Anderson Cancer Center. Cancer 2020, 126, 4905–4916. [Google Scholar] [CrossRef]
  7. Goossen, K.; Tenckhoff, S.; Probst, P.; Grummich, K.; Mihaljevic, A.L.; Büchler, M.W.; Diener, M.K. Optimal literature search for systematic reviews in surgery. Langenbecks Arch. Surg. 2018, 403, 119–129. [Google Scholar] [CrossRef]
  8. Stroup, D.F.; Berlin, J.A.; Morton, S.C.; Olkin, I.; Williamson, G.D.; Rennie, D.; Moher, D.; Becker, B.J.; Sipe, T.A.; Thacker, S.B. Meta-analysis of observational studies in epidemiology: A proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group. JAMA 2000, 283, 2008–2012. [Google Scholar] [CrossRef]
  9. Kim, D.H.; Kim, S.W.; Stybayeva, G.; Lim, S.Y.; Hwang, S.H. Predictive Value of Olfactory and Taste Symptoms in the Diagnosis of COVID-19: A Systematic Review and Meta-Analysis. Clin. Exp. Otorhinolaryngol. 2021, 14, 312–320. [Google Scholar] [CrossRef]
  10. Hwang, S.H.; Kim, J.-S.; Choi, B.Y.; Kim, J.K.; Kim, B.G. Practical Review of Olfactory Training and COVID-19. J. Rhinol. 2022, 29, 127–133. [Google Scholar] [CrossRef]
  11. Kim, D.H.; Lee, J.; Kim, S.W.; Hwang, S.H. The Efficacy of Hypotensive Agents on Intraoperative Bleeding and Recovery Following General Anesthesia for Nasal Surgery: A Network Meta-Analysis. Clin. Exp. Otorhinolaryngol. 2021, 14, 200–209. [Google Scholar] [CrossRef] [PubMed]
  12. Nichols, A.C.; Whelan, F.; Basmaji, J.; Dhaliwal, S.; Dowthwaite, S.; Chapeskie, C.; Read, N.; Palma, D.A.; Fung, K.; Venkatesan, V.; et al. Ki-67 expression predicts radiotherapy failure in early glottic cancer. J. Otolaryngol. Head Neck Surg. 2012, 41, 124–130. [Google Scholar] [PubMed]
  13. Dziegielewski, P.T.; O’Connell, D.A.; Klein, M.; Fung, C.; Singh, P.; Alex Mlynarek, M.; Fung, D.; Harris, J.R.; Seikaly, H. Primary total laryngectomy versus organ preservation for T3/T4a laryngeal cancer: A population-based analysis of survival. J. Otolaryngol. Head Neck Surg. 2012, 41 (Suppl. S1), S56–S64. [Google Scholar]
  14. Dionysopoulos, D.; Pavlakis, K.; Kotoula, V.; Fountzilas, E.; Markou, K.; Karasmanis, I.; Angouridakis, N.; Nikolaou, A.; Kalogeras, K.T.; Fountzilas, G. Cyclin D1, EGFR, and Akt/mTOR pathway. Potential prognostic markers in localized laryngeal squamous cell carcinoma. Strahlenther Onkol. 2013, 189, 202–214. [Google Scholar] [CrossRef] [PubMed]
  15. Timmermans, A.J.; Lange, C.A.; de Bois, J.A.; van Werkhoven, E.; Hamming-Vrieze, O.; Hilgers, F.J.; van den Brekel, M.W. Tumor volume as a prognostic factor for local control and overall survival in advanced larynx cancer. Laryngoscope 2016, 126, E60–E67. [Google Scholar] [CrossRef]
  16. Wong, B.Y.; Stafford, N.D.; Green, V.L.; Greenman, J. Prognostic value of the neutrophil-to-lymphocyte ratio in patients with laryngeal squamous cell carcinoma. Head Neck 2016, 38 (Suppl. S1), E1903–E1908. [Google Scholar] [CrossRef]
  17. Grover, S.; Swisher-McClure, S.; Mitra, N.; Li, J.; Cohen, R.B.; Ahn, P.H.; Lukens, J.N.; Chalian, A.A.; Weinstein, G.S.; O’Malley, B.W., Jr.; et al. Total Laryngectomy Versus Larynx Preservation for T4a Larynx Cancer: Patterns of Care and Survival Outcomes. Int. J. Radiat. Oncol. Biol. Phys. 2015, 92, 594–601. [Google Scholar] [CrossRef]
  18. Wang, J.; Wang, S.; Song, X.; Zeng, W.; Wang, S.; Chen, F.; Ding, H. The prognostic value of systemic and local inflammation in patients with laryngeal squamous cell carcinoma. Onco Targets Ther. 2016, 9, 7177–7185. [Google Scholar] [CrossRef] [Green Version]
  19. Tu, X.P.; Qiu, Q.H.; Chen, L.S.; Luo, X.N.; Lu, Z.M.; Zhang, S.Y.; Chen, S.H. Preoperative neutrophil-to-lymphocyte ratio is an independent prognostic marker in patients with laryngeal squamous cell carcinoma. BMC Cancer 2015, 15, 743. [Google Scholar] [CrossRef] [Green Version]
  20. Fu, Y.; Liu, W.; OuYang, D.; Yang, A.; Zhang, Q. Preoperative Neutrophil-to-lymphocyte Ratio Predicts Long-term Survival in Patients Undergoing Total Laryngectomy With Advanced Laryngeal Squamous Cell Carcinoma: A Single-center Retrospective Study. Medicine 2016, 95, e2689. [Google Scholar] [CrossRef]
  21. Graboyes, E.M.; Zhan, K.Y.; Garrett-Mayer, E.; Lentsch, E.J.; Sharma, A.K.; Day, T.A. Effect of postoperative radiotherapy on survival for surgically managed pT3N0 and pT4aN0 laryngeal cancer: Analysis of the National Cancer Data Base. Cancer 2017, 123, 2248–2257. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Dyckhoff, G.; Plinkert, P.K.; Ramroth, H. A change in the study evaluation paradigm reveals that larynx preservation compromises survival in T4 laryngeal cancer patients. BMC Cancer 2017, 17, 609. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Birkeland, A.C.; Beesley, L.; Bellile, E.; Rosko, A.J.; Hoesli, R.; Chinn, S.B.; Shuman, A.G.; Prince, M.E.; Wolf, G.T.; Bradford, C.R.; et al. Predictors of survival after total laryngectomy for recurrent/persistent laryngeal squamous cell carcinoma. Head Neck 2017, 39, 2512–2518. [Google Scholar] [CrossRef] [PubMed]
  24. Cheraghlou, S.; Kuo, P.; Mehra, S.; Yarbrough, W.G.; Judson, B.L. Salvage Surgery after Radiation Failure in T1/T2 Larynx Cancer: Outcomes following Total versus Conservation Surgery. Otolaryngol. Head Neck Surg. 2018, 158, 497–504. [Google Scholar] [CrossRef]
  25. Chen, L.; Zeng, H.; Yang, J.; Lu, Y.; Zhang, D.; Wang, J.; Kuang, C.; Zhu, S.; Wang, M.; Ma, X. Survival and prognostic analysis of preoperative inflammatory markers in patients undergoing surgical resection for laryngeal squamous cell carcinoma. BMC Cancer 2018, 18, 816. [Google Scholar] [CrossRef]
  26. Oh, J.; Prisman, E.; Olson, R.; Berthelet, E.; Wu, J.; Tran, E.; Bakos, B.; Kaviani, R.; Hamilton, S.N. Primary organ preservation vs total laryngectomy for T4a larynx cancer. Head Neck 2019, 41, 3265–3275. [Google Scholar] [CrossRef]
  27. Patel, S.A.; Qureshi, M.M.; Dyer, M.A.; Jalisi, S.; Grillone, G.; Truong, M.T. Comparing surgical and nonsurgical larynx-preserving treatments with total laryngectomy for locally advanced laryngeal cancer. Cancer 2019, 125, 3367–3377. [Google Scholar] [CrossRef]
  28. Zhou, T.; Yu, S.T.; Chen, W.Z.; Xie, R.; Yu, J.C. Pretreatment albumin globulin ratio has a superior prognostic value in laryngeal squamous cell carcinoma patients: A comparison study. J. Cancer 2019, 10, 594–601. [Google Scholar] [CrossRef]
  29. Song, S.; Chen, H.; Dong, W.; Zhou, H. The prognostic value of preoperative derived neutrophil-to-lymphocyte ratio in patients undergoing total laryngectomy with laryngeal carcinoma. Acta Otolaryngol. 2019, 139, 294–298. [Google Scholar] [CrossRef]
  30. Zhang, H.; Sun, M.; Zhou, D.; Gorur, A.; Sun, Z.; Zeng, W.; Cata, J.P.; Chen, W.; Miao, C. Increased mu-opioid receptor expression is associated with reduced disease-free and overall survival in laryngeal squamous cell carcinoma. Br. J. Anaesth 2020, 125, 722–729. [Google Scholar] [CrossRef]
  31. Lin, Z.; Lin, H.; Chen, Y.; Xu, Y.; Chen, X.; Fan, H.; Wu, X.; Ke, X.; Lin, C. Long-term survival trend after primary total laryngectomy for patients with locally advanced laryngeal carcinoma. J. Cancer 2021, 12, 1220–1230. [Google Scholar] [CrossRef] [PubMed]
  32. Bates, J.E.; Amdur, R.J.; Morris, C.M.; Hitchcock, K.E.; Dziegielewski, P.T.; Boyce, B.J.; Silver, N.L.; Shaw, C.; Mendenhall, W.M. Curative-dose Chemoradiotherapy Versus Total Laryngectomy For Stage T3-T4 Squamous Cell Carcinoma of the Larynx: An "Apples-to-Apples" Analysis of the National Cancer Database. Am. J. Clin. Oncol. 2019, 42, 527–533. [Google Scholar] [CrossRef] [PubMed]
  33. Parmar, M.K.; Torri, V.; Stewart, L. Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints. Stat. Med. 1998, 17, 2815–2834. [Google Scholar] [CrossRef]
  34. Tierney, J.F.; Stewart, L.A.; Ghersi, D.; Burdett, S.; Sydes, M.R. Practical methods for incorporating summary time-to-event data into meta-analysis. Trials 2007, 8, 16. [Google Scholar] [CrossRef] [Green Version]
  35. Zhou, J.; Guo, H.; Zhang, Y.; Liu, H.; Dou, Q. Prognostic significance of SHP2 (PTPN11) expression in solid tumors: A meta-analysis. PLoS ONE 2022, 17, e0262931. [Google Scholar] [CrossRef]
  36. Deeks, J.; Dinnes, J.; D’Amico, R.; Sowden, A.; Sakarovitch, C.; Song, F.; Petticrew, M.; Altman, D. Evaluating non-randomised intervention studies. Health Technol. Assess. 2003, 7, 1–173. [Google Scholar] [CrossRef] [Green Version]
  37. Sheahan, P. Management of advanced laryngeal cancer. Rambam Maimonides Med. J. 2014, 5, e0015. [Google Scholar] [CrossRef] [Green Version]
  38. Lefebvre, J.L.; Lartigau, E. Preservation of form and function during management of cancer of the larynx and hypopharynx. World J. Surg. 2003, 27, 811–816. [Google Scholar] [CrossRef]
  39. Forastiere, A.A.; Goepfert, H.; Maor, M.; Pajak, T.F.; Weber, R.; Morrison, W.; Glisson, B.; Trotti, A.; Ridge, J.A.; Chao, C.; et al. Concurrent chemotherapy and radiotherapy for organ preservation in advanced laryngeal cancer. N. Engl. J. Med. 2003, 349, 2091–2098. [Google Scholar] [CrossRef] [Green Version]
  40. Hoffman, H.T.; Porter, K.; Karnell, L.H.; Cooper, J.S.; Weber, R.S.; Langer, C.J.; Ang, K.K.; Gay, G.; Stewart, A.; Robinson, R.A. Laryngeal cancer in the United States: Changes in demographics, patterns of care, and survival. Laryngoscope 2006, 116, 1–13. [Google Scholar] [CrossRef] [Green Version]
  41. Ramos Innocentini, L.M.A.; Teixeira, A.H.; Casemiro, L.A.; Andrade, M.C.; Ferrari, T.C.; Ricz, H.M.A.; Macedo, L.D.d. Laryngeal Cancer Attributable Factors and the Influence on Survival Rates: A Single Brazilian Institution Experience. Int. Arch. Otorhinolaryngol. 2019, 23, e299–e304. [Google Scholar] [CrossRef] [Green Version]
  42. Reid, B.C.; Alberg, A.J.; Klassen, A.C.; Rozier, R.G.; Garcia, I.; Winn, D.M.; Samet, J.M. A comparison of three comorbidity indexes in a head and neck cancer population. Oral Oncol. 2002, 38, 187–194. [Google Scholar] [CrossRef] [PubMed]
  43. Charlson, M.E.; Pompei, P.; Ales, K.L.; MacKenzie, C.R. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J. Chronic. Dis. 1987, 40, 373–383. [Google Scholar] [CrossRef] [PubMed]
  44. Fong, P.Y.; Tan, S.H.; Lim, D.W.T.; Tan, E.H.; Ng, Q.S.; Sommat, K.; Tan, D.S.W.; Ang, M.K. Association of clinical factors with survival outcomes in laryngeal squamous cell carcinoma (LSCC). PLoS ONE 2019, 14, e0224665. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Cohen, E.E.; LaMonte, S.J.; Erb, N.L.; Beckman, K.L.; Sadeghi, N.; Hutcheson, K.A.; Stubblefield, M.D.; Abbott, D.M.; Fisher, P.S.; Stein, K.D.; et al. American Cancer Society Head and Neck Cancer Survivorship Care Guideline. CA Cancer J. Clin. 2016, 66, 203–239. [Google Scholar] [CrossRef]
  46. Baijal, G.; Gupta, T.; Hotwani, C.; Laskar, S.G.; Budrukkar, A.; Murthy, V.; Agarwal, J.P. Impact of comorbidity on therapeutic decision-making in head and neck cancer: Audit from a comprehensive cancer center in India. Head Neck 2012, 34, 1251–1254. [Google Scholar] [CrossRef]
  47. Sommers, L.W.; Steenbakkers, R.; Bijl, H.P.; Vemer-van den Hoek, J.G.M.; Roodenburg, J.L.N.; Oosting, S.F.; Halmos, G.B.; de Rooij, S.E.; Langendijk, J.A. Survival Patterns in Elderly Head and Neck Squamous Cell Carcinoma Patients Treated With Definitive Radiation Therapy. Int. J. Radiat Oncol. Biol. Phys. 2017, 98, 793–801. [Google Scholar] [CrossRef]
  48. Islami, F.; Tramacere, I.; Rota, M.; Bagnardi, V.; Fedirko, V.; Scotti, L.; Garavello, W.; Jenab, M.; Corrao, G.; Straif, K.; et al. Alcohol drinking and laryngeal cancer: Overall and dose-risk relation--a systematic review and meta-analysis. Oral Oncol. 2010, 46, 802–810. [Google Scholar] [CrossRef]
  49. Gastardelo, T.S.; Cunha, B.R.; Raposo, L.S.; Maniglia, J.V.; Cury, P.M.; Lisoni, F.C.; Tajara, E.H.; Oliani, S.M. Inflammation and cancer: Role of annexin A1 and FPR2/ALX in proliferation and metastasis in human laryngeal squamous cell carcinoma. PLoS ONE 2014, 9, e111317. [Google Scholar] [CrossRef] [Green Version]
  50. Bhatia, A.; Burtness, B. Novel Molecular Targets for Chemoprevention in Malignancies of the Head and Neck. Cancers 2017, 9, 113. [Google Scholar] [CrossRef] [Green Version]
  51. Cornean, C.I.; Cosgarea, M.; Cătană, A.; Mogoantă, C.A.; Necula, V.; Maniu, A.A. Do we know enough about the genetic involvement in laryngeal cancer susceptibility and prognostic outcome? Rom J. Morphol. Embryol. 2019, 60, 353–367. [Google Scholar] [PubMed]
  52. Nussbaumer-Streit, B.; Klerings, I.; Dobrescu, A.I.; Persad, E.; Stevens, A.; Garritty, C.; Kamel, C.; Affengruber, L.; King, V.J.; Gartlehner, G. Excluding non-English publications from evidence-syntheses did not change conclusions: A meta-epidemiological study. J. Clin. Epidemiol. 2020, 118, 42–54. [Google Scholar] [CrossRef] [PubMed]
Medicina 59 00497 g001 550
Figure 1. Study selection.
Figure 1. Study selection.
Medicina 59 00497 g001
Medicina 59 00497 g002 550
Figure 2. Forest plots of the effects of age (A), the Charlson comorbidity index score (B), nodal involvement (C), sex (D), and tumor location (E) on overall survival.
Figure 2. Forest plots of the effects of age (A), the Charlson comorbidity index score (B), nodal involvement (C), sex (D), and tumor location (E) on overall survival.
Medicina 59 00497 g002
Table
Table 1. The characteristics of the included studies.
Table 1. The characteristics of the included studies.
StudyDesignNumberAge, Median (Range) or
Mean (SD), y		Sex (Male/Female)NationTreatmentTumor Subsite (Supraglottic/Glottic/
Subglottic)		Laryngeal Tumor StageExtracted Outcomes
Nichols 2012 [12]Cohort75NA66/9UKRadiotherapyEarly glottis cancerT1/T2Age, gender, T stage, smoking, alcohol
Dziegielewski 2012 [13]Cohort25864.2 (36–92)205/53CanadaTL with adjuvant RT ± CT (TL-R/CT), RT, and chemotherapy–radiotherapy (CRT)Supraglottic/glottic/subglotticT3/T4a Treatment modality
Dionysopoulos 2013 [14]Cohort28963 (36–82)277/12GreeceChordectomy,
TL ± postoperative radiation		Supraglottic/glottic/subglottic/transglotticT1/T2/T3/T4Nodal involvement, tumor subsite
Zhang 2013 [2]Cohort20561.8 ± 10.6197/8ChinaTotal laryngectomy, partial laryngectomy, or CO2 laser surgery ± postoperative radiation or CTSupraglottic/glotticT1/T2/T3/T4Age, TMN stage, T stage, node involvement, tumor subsite, smoking, alcohol, Charlson score, patholic differentiation
Timmermans 2015 [15]Cohort16661.9 (11.3)124/42The NetherlandsRadiotherapy, chemoradiotherapy, or total laryngectomy with postoperative radiotherapySupraglottic/glottic/subglottic/transglotticT3/T4Treatment modality, Age, sex, T stage, node involvement
Wong 2015 [16]Cohort14066 (36–92)121/19UKPrimary surgery, surgery with adjuvant chemoradiotherapy or radiotherapy, radical radiotherapy, and chemoradiotherapyNot commentedT1/T2/T3/T4Sex, age, smoking, node involvement, TMN stage
Grover 2015 [17]Cohort96959.2 (10.4)774/195USATotal laryngectomy (TL) plus adjuvant therapy and larynx preservation chemoradiation (LP-CRT)Supraglottic/glottic/subglottic/transglotticT4aAge, TMN stage, node involvement, Charlson score, tumor subsite
Wang 2016 [18]Cohort12060.6 ± 8.6118/2ChinaTotal laryngectomy, partial laryngectomy, or CO2 laser surgery plus postoperative radiation ± CTSupraglottic/glottic/subglotticT1/T2/T3/T4 Age, smoking, alcohol, tumor subsite, T stage, node involvement, TMN stage, pathologic differentiation
Tu 2015 [19]Cohort14159 (36–87)137/4ChinaTotal laryngectomy, partial laryngectomy, or CO2 laser surgerySupraglottic/glottic/subglotticT1/T2/T3/T4T stage, node involvement
Fu 2016 [20]Cohort42060 ± 9.1 (33–84)413/7ChinaTotal laryngectomy (TL) ± adjuvant therapySupraglottic/glottic/subglotticT3/T4 Age, sex, smoking, alcohol, tumor subsite, T stage, node involvement, TMN stage, pathologic differentiation
Graboyes 2017 [21]Cohort1460NA531/143USAPartial laryngectomy or Total laryngectomy ± postoperative radiationSupraglottic/glottic/subglottic/transglotticT3 Age, sex, Charlson score, tumor subsite, pathologic differentiation
Dyckhoff 2017 [22]Cohort76961.9 (9.7)626/58GermanyPrimary chemo-radiotherapy (CRT) or primary radiotherapy alone (RT), total laryngectomy followed by adjuvant (chemo)radiotherapySupraglottic/glottic/subglottic/transglotticT4 Treatment modality, age, node involvement, tumor subsite, Charlson score
Birkeland 2017 [23]Cohort244NA208/36USATotal laryngectomy followed by adjuvant (chemo)radiotherapySupraglottic/glotticT1/T2/T3/T4 T stage
Cheraghlo 2018 [24] Cohort726NA528/198USATotal laryngectomy, open partial laryngectomy, and endoscopic partial laryngectomySupraglottic/glottic/subglottic/transglotticT1/T2 Age, sex, Charlson score, tumor subsite, T stage, node involvement
Chen 2018 [25]Cohort36160 (35–87)353/8ChinaTotal or partial laryngectomy without neoadjuvant chemotherapy or radiotherapySupraglottic/glottic/subglotticT1/T2/T3/T4Age, sex, tumor subsite, T stage, node involvement, TMN stage, pathologic differentiation
Oh 2019 [26]Cohort32962 (57–66)30/6CanadaSurgery alone, surgery with adjuvant radiotherapy (Sx/RT), radiation alone (RT), and radiation with concurrent chemoradiotherapy (chemoRT)Not describedT4aTreatment modality, age, alcohol, sex, node involvement
Patel 2019 [27]Cohort8703NA6601/2102USAChemoradiation (CRT) or partial laryngectomy (PL) and total laryngectomy (TL) with or without adjuvant therapySupraglottic/glotticT2/T3/T4Age, sex, Charlson score, pathologic differentiation, T stage, node involvement, treatment modality
Zhou 2019 [28]Cohort23263 (39–81)192/40ChinaPartial or total laryngectomy (±neck dissection) and postoperative radio-/chemotherapySupraglottic/glottic/subglotticT1/T2/T3/T4Age sex, smoking, alcohol, tumor subsite, T stage, node involvement, TMN stage, pathologic differentiation
Song 2019 [29]Cohort137NA133/4ChinaTotal laryngectomySupraglottic/glottic/subglottic/transglotticT1/T2/T3/T4Tumor subsite, age, pathologic differentiation
Bates 2019 [32]Cohort11,237NA8472/3538USAChemoradiotherapy (cRT) and total laryngectomy (TL) with adjuvant RTNot describedT3/T4Age, sex, Charlson score, T stage, node involvement, treatment modality
Boukovalas 2020 [6]Cohort36264294/68USATotal laryngectomyNot describedT1/T2/T3/T4Age, sex, T stage, node involvement, smoking, alcohol
Zhang 2020 [30]Cohort207NA198/9ChinaPartial or total laryngectomySupraglottic/glottic/subglottic/transglotticT1/T2/T3/T4Age, sex, alcohol, smoking, pathologic differentiation, TMN stage, T stage, node involvement
Lin 2021 [31] Cohort2094NA1712/382ChinaTotal laryngectomySupraglottic/glotticT1/T2/T3/T4Age, sex, pathologic differentiation, node involvement
Voora 2021Cohort104362.29 (8.13)1039/4USAChemoradiotherapy (cRT) and total laryngectomy (TL) with adjuvant RTSupraglottic/glottic/subglottic/transglotticT4aAge, sex, Charlson score, alcohol, tumor subsite, smoking, node involvement, treatment modality
Zhang 2021Cohort21162.19 (8.328)164/47ChinaTotal or partial laryngectomy ± Adjuvant radiotherapySupraglottic/glottic/subglottic/transglotticT1/T2/T3/T4Sex, alcohol, tumor subsite, smoking, node involvement, TMN stage, pathologic differentiation
Geng 2022Cohort7858.1 (51.1–62.1)70/8USATotal or partial laryngectomy ± Adjuvant radiotherapySupraglottic/glottic/subglotticT1/T2/T3/T4Age, sex, tumor subsite, smoking, TMN stage, pathologic differentiation
Lin 2022 [31]Cohort15460.90 (9.79)147/7ChinaTotal or partial laryngectomy ± Adjuvant radiotherapySupraglottic/glottic/subglotticT1/T2/T3/T4Age, sex, alcohol, smoking, TMN stage, treatment modality
Zhu 2022Cohort99856–70946/52ChinaChemoradiotherapy (cRT) and total laryngectomy (TL) with adjuvant RTSupraglottic/glottic/subglotticT1/T2/T3/T4Age, sex, tumor subsite, TMN stage, pathologic differentiation
CRT; chemoradiation therapy, TL; total laryngectomy, RT; radiation therapy, HR; Hazard ratio.
Table
Table 2. Predictive values of various risk factors.
Table 2. Predictive values of various risk factors.
Overall SurvivalDisease-Free Survival
Age (≥60 vs. 60)n = 21n = 9
1.1300 [1.0908; 1.1705]; p < 0.0001; I2 = 91.5%1.0070 [1.0005; 1.0136]; p = 0.0359; I2 = 15.9%
Sex (male vs. female)n = 13n = 8
0.9856 [0.8866; 1.0956]; p = 0.7883; I2 = 53.9% 1.1047 [0.7234; 1.6869]; p = 0.6448; I2 = 84.7%
Smoking (yes vs. no)n = 11n = 9
1.2926 [1.0999; 1.5191]; p = 0.0018; I2 = 13.6%1.2237 [0.9206; 1.6267]; p = 0.1644; I2 = 61.2%
Alcohol (yes vs. no)n = 9n = 7
1.1979 [1.0696; 1.3415]; p = 0.0018; I2 = 33.1%1.1861 [0.9588; 1.4673]; p = 0.1159; I2 = 54.1%
Charlson score (≥2 vs. 0 or 1)n = 8
1.6716 [1.3533; 2.0647]; p < 0.0001; I2 = 86.6%
Charlson score (1 vs. 0)n = 5
1.3153 [1.2299; 1.4068]; p < 0.0001; I2 = 12.1%
TNM stage (III and IV vs. I and II)n = 9n = 10
2.4583 [1.8323; 3.2980]; p < 0.0001; I2 = 81.9%2.3987 [2.0956; 2.7456]; p < 0.0001; I2 = 29.8%
Tumor stage (III and IV vs. I and II)n = 10n = 5
1.5648 [1.2363; 1.9806]; p < 0.0001; I2 = 86.4%1.8441 [1.4507; 2.3441]; p< 0.0001; I2 = 0.0%
Tumor location (subglottis vs. glottis)n = 4
1.3956 [0.5841; 3.3341]; p = 0.4532; I2 = 84.1%
Tumor location (supraglottic vs. glottis)n = 11n = 4
1.3740 [1.0730; 1.7594]; p = 0.0118; I2 = 82.3%1.6371 [1.0162; 2.6373]; p < 0.0001; I2 = 90.2%
Tumor location (transglottic vs. glottis)n = 5
1.3699 [0.9348; 2.0076]; p = 0.1065; I2 = 69.3%
Node involvement (yes vs. no)n = 16n = 10
1.9439 [1.6235; 2.3276]; p < 0.0001; I2 = 87.6%1.6174 [1.4560; 1.7968]; p < 0.0001; I2 = 46.6%
Pathologic differentiation (moderate vs. high)n = 6
1.2820 [1.0659; 1.5419]; p < 0.0001; I2 = 51.3%
Pathologic differentiation (poor vs. high)n = 9n = 3
1.6951 [1.5394; 1.8665]; p < 0.0001; I2 = 43.2%1.5336 [0.7875; 2.9864]; p = 0.2086; I2 = 90.1%
Treatment modality (primary chemoradiotherapy vs. total laryngectomy)n = 10
1.4004 [1.1639; 1.6850]; p = 0.0004; I2 = 90.6%
Treatment modality (primary radiotherapy vs. total laryngectomy)n = 8
1.5418 [1.1531; 2.0616]; p = 0.0035; I2 = 91.6%
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Kim, D.H.; Kim, S.W.; Han, J.S.; Kim, G.-J.; Basurrah, M.A.; Hwang, S.H. The Prognostic Utilities of Various Risk Factors for Laryngeal Squamous Cell Carcinoma: A Systematic Review and Meta-Analysis. Medicina 2023, 59, 497. https://doi.org/10.3390/medicina59030497

AMA Style

Kim DH, Kim SW, Han JS, Kim G-J, Basurrah MA, Hwang SH. The Prognostic Utilities of Various Risk Factors for Laryngeal Squamous Cell Carcinoma: A Systematic Review and Meta-Analysis. Medicina. 2023; 59(3):497. https://doi.org/10.3390/medicina59030497

Chicago/Turabian Style

Kim, Do Hyun, Sung Won Kim, Jae Sang Han, Geun-Jeon Kim, Mohammed Abdullah Basurrah, and Se Hwan Hwang. 2023. "The Prognostic Utilities of Various Risk Factors for Laryngeal Squamous Cell Carcinoma: A Systematic Review and Meta-Analysis" Medicina 59, no. 3: 497. https://doi.org/10.3390/medicina59030497

APA Style

Kim, D. H., Kim, S. W., Han, J. S., Kim, G. -J., Basurrah, M. A., & Hwang, S. H. (2023). The Prognostic Utilities of Various Risk Factors for Laryngeal Squamous Cell Carcinoma: A Systematic Review and Meta-Analysis. Medicina, 59(3), 497. https://doi.org/10.3390/medicina59030497

Article Metrics

Back to TopTop