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Progression-free survival as surrogate endpoint of overall survival in esophageal squamous cell carcinoma: a real-world data and literature-based analysis

BACKGROUND: The surrogacy of progression-free survival (PFS) for overall survival (OS) in esophageal squamous cell carcinoma (ESCC) remains unelucidated. This study aimed to determine the validity of PFS as a surrogate endpoint for OS in ESCC patients treated with definitive radiotherapy or definiti...

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Detalles Bibliográficos
Autores principales: Han, Weiming, Wang, Lan, Li, Chen, Chen, Junqiang, Zhang, Wencheng, Wang, Xin, Pang, Qingsong, Zhao, Yidian, Sun, Xinchen, Zhang, Kaixian, Li, Gaofeng, Li, Ling, Qiao, Xueying, Liu, Miaoling, Wang, Yadi, Deng, Lei, Wang, Wenqing, Bi, Nan, Zhang, Tao, Deng, Wei, Ni, Wenjie, Chang, Xiao, Zhou, Zongmei, Liang, Jun, Feng, Qinfu, Wang, Lvhua, Chen, Dongfu, Lv, Jima, Zhu, Shuchai, Han, Chun, Xiao, Zefen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619262/
https://www.ncbi.nlm.nih.gov/pubmed/36324733
http://dx.doi.org/10.1177/17588359221131526
Descripción
Sumario:BACKGROUND: The surrogacy of progression-free survival (PFS) for overall survival (OS) in esophageal squamous cell carcinoma (ESCC) remains unelucidated. This study aimed to determine the validity of PFS as a surrogate endpoint for OS in ESCC patients treated with definitive radiotherapy or definitive chemoradiotherapy (dRT/dCRT), as well as characterize the prognostic factors and survival of such patients. METHODS: A total of 3662 patients from 10 cancer centers were enrolled. One-, 2-, and 3-year PFS (PFS12, PFS24, and PSF36, respectively) were used as time points for analysis. At each time point, ESCC-specific mortality and OS were characterized using competing risk and conditional survival models, while correlation between PFS and OS was evaluated by linear regression. RESULTS: At PFS12, PFS24, and PFS36, a progressive decrease in 5-year ESCC-specific mortality (35.2%–13.4%) and increase in 5-year OS (46.6%–62.9%) were observed. Regardless, the OS of patients remained markedly lower than those of the age- and sex-matched Chinese general population. TNM stage remained a significant prognostic factor at PFS36. Strong correlation was found between 3-year PFS and 5-year OS, which was further externally validated. CONCLUSIONS: Three-year PFS may act as a potential surrogate endpoint for 5-year OS. TNM stage was considered a significant prognostic factor for OS, and may represent the optimal prognostic tool to guide clinical decision-making and post-treatment follow-up.