Open AccessTiming of chemotherapy‐induced neutropenia is a prognostic factor in patients with advanced gastric cancer undergoing first‐line chemotherapy with oxaliplatin and capecitabine: a retrospective study
Author(s) -
Wang Yanrong,
Chen Yang,
Yin Hongyan,
Gu Xiaobin,
Shi Yan,
Dai Guanghai
Publication year - 2018
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.1308
Subject(s) - capecitabine , oxaliplatin , medicine , hazard ratio , chemotherapy , oncology , proportional hazards model , neutropenia , cancer , retrospective cohort study , confidence interval , gastroenterology , colorectal cancer
Chemotherapy‐induced neutropenia ( CIN ) has been shown to be associated with improved clinical outcomes in patients with various solid tumors. This study retrospectively assessed the association between timing of CIN and prognosis in 321 patients with advanced gastric cancer ( AGC ) who finished at least one cycle of chemotherapy with oxaliplatin and capecitabine ( XELOX ). Primary landmark analyses were restricted to 274 patients who received four cycles of chemotherapy and lived for more than 4 months. CIN was categorized as early‐onset and non‐early‐onset. The correlation between timing of CIN with survival was analyzed by the Kaplan‐Meier method and a Cox proportional hazards model. Relative to patients with non‐early‐onset CIN , those with early‐onset CIN had significantly longer times to disease progression (hazard ratio [ HR ] 0.574; 95% confidence interval [ CI ] 0.453–0.729, P < 0.001) and death ( HR : 0.607; 95% CI : 0.478–0.770, P < 0.001), consistent with results from the landmark group. In conclusion, timing of CIN may be a potential prognostic biomarker in patients with AGC receiving first‐line chemotherapy with XELOX . Early‐onset CIN predicts better survival.