scholarly journals State of the art treatment for stage I to III anal squamous cell carcinoma: A systematic review and meta-analysis

2021 ◽  
Vol 157 ◽  
pp. 188-196
Author(s):  
Ricardo N. Werner ◽  
Matthew Gaskins ◽  
Gabriela Avila Valle ◽  
Volker Budach ◽  
Stephan Koswig ◽  
...  
2018 ◽  
Vol 10 (1) ◽  
pp. 48-60 ◽  
Author(s):  
Marcos Pedro Guedes Camandaroba ◽  
Raphael Leonardo Cunha de Araujo ◽  
Virgílio Souza e Silva ◽  
Celso Abdon Lopes de Mello ◽  
Rachel P. Riechelmann

2017 ◽  
Vol 6 (3) ◽  
pp. 463-473 ◽  
Author(s):  
Jian-Ning Yao ◽  
Xue-Xiu Zhang ◽  
Hai-Ning Zhou ◽  
Yan-Le Li ◽  
Hong-Rui Xu ◽  
...  

Biomedicines ◽  
2021 ◽  
Vol 9 (5) ◽  
pp. 486
Author(s):  
Juan P. Rodrigo ◽  
Mario Sánchez-Canteli ◽  
Fernando López ◽  
Gregory T. Wolf ◽  
Juan C. Hernández-Prera ◽  
...  

The presence of tumor-infiltrating lymphocytes (TIL) in the tumor microenvironment has been demonstrated to be of prognostic value in various cancers. In this systematic review and meta-analysis, we investigated the prognostic value of TIL in laryngeal squamous cell carcinoma (LSCC). We performed a systematic search in PubMed for publications that investigated the prognostic value of TIL in LSCC. A meta-analysis was performed including all studies assessing the association between TIL counts in hematoxylin-eosin (HE)-stained sections, for CD8+ and/or CD3+/CD4+ TIL and overall survival (OS) or disease-free survival (DFS). The pooled meta-analysis showed a favorable prognostic role for stromal TIL in HE sections for OS (HR 0.57, 95% CI 0.36–0.91, p = 0.02), and for DFS (HR 0.56, 95% CI 0.34–0.94, p = 0.03). High CD8+ TIL were associated with a prolonged OS (HR 0.62, 95% CI 0.4–0.97, p = 0.04) and DFS (HR 0.73, 95% CI 0.34–0.94, p = 0.002). High CD3+/CD4+ TIL demonstrated improved OS (HR 0.32, 95% CI 0.16–0.9, p = 0.03) and DFS (HR 0.23, 95% CI 0.10–0.53, p = 0.0005). This meta-analysis confirmed the favorable prognostic significance of TIL in LSCC. High stromal TIL evaluated in HE sections and intra-tumoral and stromal CD3+, CD4+ and/or CD8+ TIL might predict a better clinical outcome.


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