Medical Oncology Department 2, Chinese People's Liberation Army General Hospital, Beijing, 100853, China.
Department of Radiation Oncology, First Hospital of Peking University, Beijing, 100034, China.
Cancer Med. 2018 Apr;7(4):997-1005. doi: 10.1002/cam4.1308. Epub 2018 Mar 13.
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.
化疗引起的中性粒细胞减少症(CIN)已被证明与各种实体瘤患者的临床结局改善相关。本研究回顾性评估了 321 例接受奥沙利铂和卡培他滨(XELOX)化疗至少一个周期的晚期胃癌(AGC)患者中 CIN 发生时间与预后之间的关系。主要里程碑分析仅限于接受了 4 个周期化疗且生存期超过 4 个月的 274 例患者。将 CIN 分为早发性和非早发性。采用 Kaplan-Meier 方法和 Cox 比例风险模型分析 CIN 发生时间与生存的相关性。与非早发性 CIN 患者相比,早发性 CIN 患者的疾病进展时间(风险比 [HR] 0.574;95%置信区间 [CI] 0.453-0.729,P<0.001)和死亡时间(HR:0.607;95%CI:0.478-0.770,P<0.001)显著延长,与里程碑组的结果一致。总之,在接受 XELOX 一线化疗的 AGC 患者中,CIN 的发生时间可能是一个潜在的预后生物标志物。早发性 CIN 预示着更好的生存。