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Timing of chemotherapy-induced neutropenia: the prognostic factor in advanced pancreatic cancer patients treated with gemcitabine / gemcitabine-based chemotherapy

机译:化疗诱发的中性粒细胞减少症的时机:吉西他滨/吉西他滨为基础的化疗治疗晚期胰腺癌患者的预后因素

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摘要

Chemotherapy-induced neutropenia (CIN) was reported to be a predictor of better survival in several cancers. The objective of our study is to evaluate the relationship between the timing (onset) of CIN and prognosis. Between June 2008 and June 2015, 134 patients with confirmed advanced pancreatic cancer received at least one cycle of gemcitabine / gemcitabine-based chemotherapy as first-line chemotherapy were eligible for assessment. Timing of CIN was categorized into early onset and non-early onset CIN group. The end of cycle 2 was the cutoff to differentiate early onset or non-early onset. The correlation between timing of CIN with survival was analyzed by Kaplan-Meier method and Cox proportional hazards model. Median overall survival (OS) was 8.05 months (95% CI: 5.97-10.13) for patients with early onset CIN compared with 5.82 months (95% CI: 5.00-6.63) for patients without early-onset neutropenia (P = 0.022). Multivariate analysis proved that timing of CIN was an independent prognostic factor, hazard ratios of death was 0.696 (95% CI: 0.466-0.938) for patients with early onset CIN. In conclusion, timing of CIN is an independent predictor of prognosis in patients with advanced pancreatic cancer undergoing gemcitabine / gemcitabine based chemotherapy. Early-onset CIN predicts better survival.
机译:据报道,化学疗法诱发的中性粒细胞减少症(CIN)是几种癌症中较好生存的预测指标。我们研究的目的是评估CIN的时机(发作)与预后之间的关系。在2008年6月至2015年6月期间,有134名确诊为晚期胰腺癌的患者接受了至少一个周期的吉西他滨/基于吉西他滨的化学疗法作为一线化疗的评估。 CIN的时机分为早期发作和非早期发作的CIN组。周期2的结束是区分早期发作或非早期发作的临界点。用Kaplan-Meier法和Cox比例风险模型分析了CIN的时机与生存的相关性。早发性CIN患者的中位总生存期(OS)为8.05个月(95%CI:5.97-10.13),而早发性中性粒细胞减少症的患者的中位总生存期(OS)为5.82个月(95%CI:5.00-6.63)(P = 0.022)。多因素分析证明,CIN的时机是独立的预后因素,CIN早发患者的死亡危险比为0.696(95%CI:0.466-0.938)。总之,CIN的时机是接受吉西他滨/吉西他滨为基础化疗的晚期胰腺癌患者预后的独立预测指标。早期发作的CIN可以预测更好的生存率。

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