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粒细胞集落刺激因子对化疗剂量强度和癌症生存的影响:一项随机对照试验的系统评价和荟萃分析。

The impact of the granulocyte colony-stimulating factor on chemotherapy dose intensity and cancer survival: a systematic review and meta-analysis of randomized controlled trials.

机构信息

Department of Medicine, Duke University, Durham.

Department of Medicine, University of Washington, Seattle, USA.

出版信息

Ann Oncol. 2013 Oct;24(10):2475-2484. doi: 10.1093/annonc/mdt226. Epub 2013 Jun 20.

Abstract

BACKGROUND

The granulocyte colony-stimulating factor (G-CSF) is utilized to reduce neutropenic complications in patients receiving cancer chemotherapy. This study represents a systematic review and evidence summary of the impact of G-CSF support on chemotherapy dose intensity and overall mortality.

MATERIALS AND METHODS

All randomized controlled trials (RCTs) comparing chemotherapy with or without G-CSF support and reporting all-cause mortality with at least 2 years of follow-up were sought. Dual-blind data abstraction of disease, treatment, patient and outcome study results with conflict resolution by third party was carried out.

RESULTS

The search revealed 61 randomized comparisons of chemotherapy with or without initial G-CSF support. Death was reported in 4251 patients randomized to G-CSFs and in 5188 controls. Relative risk (RR) with G-CSF support for all-cause mortality was 0.93 (95% confidence interval: 0.90-0.96; P < 0.001). RR for mortality varied by intended chemotherapy dose and schedule: same dose and schedule (RR = 0.96; P = 0.060), dose dense (RR = 0.89; P < 0.001), dose escalation (RR = 0.92; P = 0.019) and drug substitution or addition (RR = 0.94; P = 0.003). Greater RR reduction was observed among studies with longer follow-up (P = 0.02), where treatment was for curative intent (RR = 0.91; P < 0.001), and where survival was the primary outcome (RR = 0.91; P < 0.001).

CONCLUSIONS

All-cause mortality is reduced in patients receiving chemotherapy with primary G-CSF support. The greatest impact was observed in RCTs in patients receiving dose-dense schedules.

摘要

背景

粒细胞集落刺激因子(G-CSF)用于减少接受癌症化疗的患者中性粒细胞减少症的并发症。本研究对 G-CSF 支持对化疗剂量强度和总死亡率的影响进行了系统评价和证据总结。

材料和方法

检索了所有比较化疗加或不加 G-CSF 支持并报告至少 2 年随访全因死亡率的随机对照试验(RCT)。对疾病、治疗、患者和结局研究结果进行了双盲数据提取,并由第三方解决冲突。

结果

搜索结果显示,61 项化疗加或不加初始 G-CSF 支持的随机比较。在接受 G-CSF 治疗的 4251 例患者和对照组的 5188 例患者中报告了死亡。G-CSF 支持组全因死亡率的相对风险(RR)为 0.93(95%置信区间:0.90-0.96;P<0.001)。RR 因拟议的化疗剂量和方案而异:相同剂量和方案(RR=0.96;P=0.060)、剂量密集(RR=0.89;P<0.001)、剂量递增(RR=0.92;P=0.019)和药物替代或添加(RR=0.94;P=0.003)。随访时间较长(P=0.02)、治疗为治愈性目的(RR=0.91;P<0.001)和生存为主要结局(RR=0.91;P<0.001)的研究中,RR 降低更为显著。

结论

接受 G-CSF 支持的化疗患者全因死亡率降低。在接受密集剂量方案的 RCT 中观察到最大影响。

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