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Cited 48 time in webofscience Cited 55 time in scopus
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Nivolumab in previously treated advanced gastric cancer (ATTRACTION-2): 3-year update and outcome of treatment beyond progression with nivolumab

Authors
Boku, NarikazuSatoh, TarohRyu, Min-HeeChao, YeeKato, KenChung, Hyun CheolChen, Jen-ShiMuro, KeiKang, Won KiYeh, Kun-HueiYoshikawa, TakakiOh, Sang CheulBai, Li-YuanTamura, TakaoLee, Keun-WookHamamoto, YasuoKim, Jong GwangChin, KeishoOh, Do-YounMinashi, KeikoCho, Jae YongTsuda, MasahiroNishiyama, TaiheiChen, Li-TzongKang, Yoon-Koo
Issue Date
Jul-2021
Publisher
SPRINGER
Keywords
ATTRACTION-2; Gastric or gastroesophageal junction cancer; Nivolumab; Long-term efficacy; Treatment beyond progression
Citation
GASTRIC CANCER, v.24, no.4, pp 946 - 958
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
GASTRIC CANCER
Volume
24
Number
4
Start Page
946
End Page
958
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/52584
DOI
10.1007/s10120-021-01173-w
ISSN
1436-3291
1436-3305
Abstract
Background ATTRACTION-2 demonstrated that nivolumab improved overall survival (OS) vs placebo in patients with advanced gastric cancer treated with >= 2 chemotherapy regimens. However, its long-term efficacy and outcome of treatment beyond progression (TBP) with nivolumab have not been clarified. Methods The 3-year follow-up data were collected. A subset analysis was performed to explore the efficacy of TBP by assessing postprogression survival (PPS) after the first event of disease progression. Results Overall, 493 patients were randomized (2:1) to receive nivolumab (n = 330) or placebo (n = 163). With a median follow-up of 38.5 (range 36.1-47.5) months, OS of the nivolumab group was significantly longer compared to the placebo group (median 5.3 vs 4.1 months; 3-year survival rate, 5.6% vs 1.9%; hazard ratio [HR], 0.62 [95% confidence interval (CI) 0.50-0.75], P < 0.0001). The median OS of responders (n = 32) who achieved complete response or partial response was 26.7 months and the 3-year survival rate was 35.5% in the nivolumab group. Overall, 109 patients in the nivolumab group and 37 patients in the placebo group received TBP. PPS tended to be longer in the nivolumab group vs placebo group (median 5.8 vs 4.5 months; HR [95% CI], 0.69 [0.47-1.01], P = 0.057). In contrast, PPS was similar between both treatment groups in non-TBP patients (median 2.3 vs 2.2 months; HR 0.90, P = 0.42). Conclusions Long-term efficacy of nivolumab was confirmed at the 3-year follow-up, and a survival benefit of TBP with nivolumab was suggested. Biomarkers for selecting patients suitable for TBP with nivolumab should be identified in the future.
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Guro Hospital (Department of Medical Oncology and Hematology, Guro Hospital)
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