@article{d9171834bde84ff5ada010126efc0c37,
title = "Exploration of predictors of benefit from nivolumab monotherapy for patients with pretreated advanced gastric and gastroesophageal junction cancer: post hoc subanalysis from the ATTRACTION-2 study",
abstract = "Background: The phase 3 ATTRACTION-2 study demonstrated that nivolumab monotherapy was superior to placebo for patients with pretreated advanced gastric or gastroesophageal junction cancer, but early progression of tumors in some patients was of concern. Methods: This post hoc analysis statistically explored the baseline characteristics of the ATTRACTION-2 patients and extracted a single-factor and double-factor combinations associated with early disease progression or early death. In the extracted patient subgroups, the 3-year restricted mean survival times of progression-free survival and overall survival were compared between the nivolumab and placebo arms. Results: Two single factors (age and peritoneal metastasis) were extracted as independent predictors of early progression, but none of them, as a single factor, stratified patients into two subgroups with significant differences in restricted mean survival time. In contrast, two double-factor combinations (serum sodium level and white blood cell count; serum sodium level and neutrophil–lymphocyte ratio) stratifying patients into two subgroups with significant differences in the restricted mean survival time were extracted. Additional exploratory analysis of a triple-factor combination showed that patients aged < 60 years with peritoneal metastasis and low serum sodium levels (approximately 7% of all patients) might receive less benefit from nivolumab, and patients aged ≥ 60 years with no peritoneal metastasis and normal serum sodium levels might receive higher benefit. Conclusions: A combination of age, peritoneal metastasis, and serum sodium level might predict benefit from nivolumab as salvage therapy in advanced gastric or gastroesophageal junction cancer patients, especially less benefit for patients having all three risk factors.",
keywords = "Benefit predictors, Early progression, Gastric cancer, Gastroesophageal junction, Nivolumab",
author = "Kang, {Yoon Koo} and Satoshi Morita and Taroh Satoh and Ryu, {Min Hee} and Yee Chao and Ken Kato and Chung, {Hyun Cheol} and Chen, {Jen Shi} and Kei Muro and Kang, {Won Ki} and Yeh, {Kun Huei} and Takaki Yoshikawa and Oh, {Sang Cheul} and Bai, {Li Yuan} and Takao Tamura and Lee, {Keun Wook} and Yasuo Hamamoto and Kim, {Jong Gwang} and Keisho Chin and Oh, {Do Youn} and Keiko Minashi and Cho, {Jae Yong} and Masahiro Tsuda and Hiroki Sameshima and Chen, {Li Tzong} and Narikazu Boku",
note = "Funding Information: All authors received grants from Ono Pharmaceutical Co., Ltd., and Bristol-Myers Squibb for the work under consideration for publication. Y-KK reports personal fees from Ono, Bristol-Myers Squibb, Daehwa, Blueprint, Merck, and Astellas, outside the submitted work. MS reports personal fees from Ono, Bristol-Myers Squibb, AstraZeneca, Chugai, Eli Lilly Japan, MSD, Pfizer Japan, and Taiho, outside the submitted work. TS reports personal fees from Ono for the work under consideration for publication; other from Ono (endorsed Department, lecture fee); grants, personal fees, and other from Chugai and Yakult Honsha (endorsed Department, lecture fee); grants and other from Eli Lilly (lecture fee), grants from MSD, Gilead Sciences, Parexel, and Daiichi Sankyo, and Astellas; grants and personal fees from Taiho, personal fees from Takara-Bio, outside the submitted work. M-HR reports honorarium and advisory board fees from Ono, Bristol-Myers Squibb, MSD, Eli Lilly, Taiho, Novartis, Daiichi Sankyo, AstraZeneca, and Daehwa, outside the submitted work. KK reports research funding from Merck & Co., Shionogi, Ono, MSD, Merck Serono, and BeiGene, outside the submitted work. HCC reports grants (research support) from Eli Lilly, GlaxoSmithKline, MSD, Merck Serono, Bristol-Myers Squibb, Ono, Taiho, Amgen, BeiGene, Incyte, and Zymework; personal fees (honoraria) from Merck Serono, Eli Lilly, Foundation Medicine, and Roche; and personal fees (consultation) from Taiho, Celltrion, MSD, Eli Lilly, Quintiles, Bristol-Myers Squibb, Merck Serono, Gloria, BeiGene, Amgen, and Zymeworks, outside the submitted work. J-SC reports personal fees (consultation) from Ono for the work under consideration for publication. KMu reports grants and personal fees from Ono, Sanofi, Taiho, and Amgen; grants from MSD, Daiichi Sankyo, Parexel International, Pfizer, Solasia, and Merck Serono; and personal fees from AstraZeneca, Eli Lilly, Chugai, Takeda, Bristol-Myers Squibb, and Bayer, outside the submitted work. K-HY reports personal fees (honoraria) from Ono, Bristol-Myers Squibb, Boehringer Ingelheim, Takeda, MSD, Eli Lilly, Amgen, and Roche, outside the submitted work. TY reports grants and personal fees (honoraria) from Chugai and Taiho; personal fees (honoraria) from Bristol-Myers Squibb; and personal fees (honoraria and advisory role) from Ono, outside the submitted work. TT reports grants from MSD, Merck Serono, and Chugai; and grants and personal fees from Daiichi Sankyo, Takeda, and Taiho, outside the submitted work. K-WL reports grants from MSD, AstraZeneca/MedImmune, Merck KGaA, Pfizer, BeiGene, ALX Oncology, Zymeworks, MacroGenics, Five Prime Therapeutics, Oncologie, Pharmacyclics, Green Cross Corp, ABLBIO, Y-BIOLOGICS, Genexine, LSK BioPharma, Daiichi Sankyo, Taiho (to his institution for conducting clinical trials), personal fees (consultation) from ISU ABXIS, Bayer and Daiichi Sankyo, outside the submitted work. KC reports personal fees from Ono, Bristol-Myers Squibb, Taiho, and Chugai, outside the submitted work. D-YO reports grants from AstraZeneca outside the submitted work. KMi reports research funding from MSD, Merck Biopharma, Astellas, Taiho., and Daiichi Sankyo, outside the submitted work. HS is an employee of Ono. L-TC reports personal fees from Ono and Bristol-Myers Squibb for the work under consideration for publication; grants from the Ministry of Science and Technology (Taiwan), Ministry of Health and Welfare (Taiwan), grants, personal fees and non-financial support from Novartis (study medication and funding support, and honorarium), grants from Pfizer (study funding), personal fees from Eli Lilly (honorarium), grants from Merck Serono (study funding), grants, personal fees and non-financial support from TTY (study medication and funding support, and honorarium), personal fees from PharmaEngine, Shire, MSD, Bristol-Myers Squibb, and Ono (honorarium), grants from OBI (preclinical testing), grants from Polaris (translational Research funding), grants, personal fees and non-financial support from SynCore (study medication and funding support, and honorarium), grants and non-financial support from Celgene (study medication and funding), and personal fees from Five Prime, and Merrimack{\textquoteright} outside the submitted work. NB reports personal fees from Ono and Bristol-Myers Squibb for the work under consideration for publication; grants and personal fees from Taiho and grants from Takeda, outside the submitted work. Funding Information: We thank the patients who participated in ATTRACTION-2 and their supportive families. We also thank the investigators and staff at all study sites for their contributions to ATTRACTION-2. Medical writing support, including drafting of the manuscript, assembling of tables, and creation of images based on the authors{\textquoteright} directions, was provided by Masatoshi Esaki, PhD, of Ono Pharmaceutical Co., Ltd., Osaka, Japan, and this study was funded by Ono Pharmaceutical Co., Ltd. and Bristol-Myers Squibb, Princeton, NJ, USA. Publisher Copyright: {\textcopyright} 2021, The Author(s).",
year = "2022",
month = jan,
doi = "10.1007/s10120-021-01230-4",
language = "English",
volume = "25",
pages = "207--217",
journal = "Gastric Cancer",
issn = "1436-3291",
publisher = "Springer Japan",
number = "1",
}