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Published on: November 30, 2016
Association of Cachexia-Related Status With Treatment Outcomes in Advanced Gastric Cancer Receiving First-Line
Hironori Fujii1, Daichi Watanabe2,3, Yunami Yamada2
1Department of Pharmacy, Gifu University Hospital, 1-1 Yanagido, Gifu, 501-1194, Japan. fujii.hironori.u5@f.gifu-u.ac.jp.
Purpose:
The clinical significance of longitudinal cachexia-related status during first-line therapy for advanced gastric cancer remains unclear in the era of nivolumab-containing chemotherapy. We evaluated its association with outcomes according to nivolumab use.
Methods:
We retrospectively analyzed 121 patients with HER2-negative unresectable advanced or recurrent gastric cancer who received first-line oxaliplatin- plus fluoropyrimidine-based chemotherapy between 2017 and 2024. Modified Glasgow Prognostic Score (mGPS) 2 status and modified European Palliative Care Research Collaborative (EPCRC)-defined cachexia status were assessed as time-dependent covariates. Progression-free survival (PFS) and overall survival (OS) were analyzed using time-dependent Cox proportional hazards models.
Results:
The cohort included 69 patients in the non-nivolumab group and 52 in the nivolumab-containing group. Median age was 71 years, 76 patients (63%) were male, and baseline mGPS 2 was present in 37 patients (31%). The cumulative proportion of patients who met the mGPS 2 criterion by 6 months was 55% in the non-nivolumab group and 57% in the nivolumab-containing group. Time-dependent mGPS 2 status was not significantly associated with PFS (hazard ratio [HR], 1.49; 95% confidence interval [CI], 0.69-3.20; P = 0.30), but was associated with shorter OS (HR, 2.17; 95% CI, 1.15-4.10; P = 0.017). No statistically significant interaction between time-dependent mGPS 2 status and nivolumab use was observed for PFS or OS. Time-dependent modified EPCRC-defined cachexia status was not significantly associated with PFS or OS.
Conclusions:
Time-dependent mGPS 2 status during first-line therapy was associated with shorter OS, but not PFS.
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