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辅助 TC 或 FEC-D 化疗方案在临床试验以外的环境中应用初级 G-CSF 预防:系统评价和荟萃分析。

Primary G-CSF prophylaxis for adjuvant TC or FEC-D chemotherapy outside of clinical trial settings: a systematic review and meta-analysis.

机构信息

Atlantic Clinical Cancer Research Unit, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Support Care Cancer. 2012 Oct;20(10):2523-30. doi: 10.1007/s00520-011-1375-6. Epub 2012 Jan 15.

Abstract

BACKGROUND

Variable febrile neutropenia (FN) rates reported with adjuvant TC (taxotere®, cyclophosphamide) and FEC-D (5-flurouracil, epirubicin, cyclophosphamide, docetaxel) outside of clinical trials have precluded definitive recommendations for primary G-CSF (granulocyte colony-stimulating factor) prophylaxis in most jurisdictions. A systematic review and meta-analysis was conducted to assess: (a) FN rates associated with TC and FEC-D without primary G-CSF prophylaxis outside of clinical trial settings, and (b) the potential impact of G-CSF prophylaxis on FN prevention.

METHODS

A MEDLINE search was conducted and major conference abstracts were reviewed up to June 15th 2011 to identify all relevant English-language studies. Random- and fixed-effects meta-analysis models were performed.

RESULTS

Nine hundred two patients treated with TC and 1342 with FEC-D from 13 to 9 studies, respectively, were included. The pooled random-effects meta-analysis estimates of FN rates for TC and FEC-D without G-CSF were 29% (95% CI 24-35%) and 31% (95% CI 27-35%), with a 76% (RR = 0.24, 95% CI 0.14-0.41) and 63% (RR = 0.37, 95% CI 0.11-1.24) relative risk reduction with G-CSF, respectively.

CONCLUSION

In routine clinical practice, TC and FEC-D without G-CSF are associated with FN rates exceeding the 20% threshold for which primary G-CSF prophylaxis is commonly recommended, and are considerably higher than those reported in pivotal clinical trials.

摘要

背景

TC(多西他赛®,环磷酰胺)和 FEC-D(5-氟尿嘧啶,表柔比星,环磷酰胺,多西他赛)辅助治疗的发热性中性粒细胞减少症(FN)发生率在临床试验之外变化不定,这使得在大多数司法管辖区无法对初级 G-CSF(粒细胞集落刺激因子)预防提出明确建议。进行了系统评价和荟萃分析,以评估:(a)在临床试验之外无初级 G-CSF 预防的 TC 和 FEC-D 相关 FN 发生率,以及(b)G-CSF 预防对 FN 预防的潜在影响。

方法

进行了 MEDLINE 检索,并查阅了截至 2011 年 6 月 15 日的主要会议摘要,以确定所有相关的英文研究。采用随机效应和固定效应荟萃分析模型。

结果

纳入了分别来自 13 项和 9 项研究的 902 例接受 TC 治疗和 1342 例接受 FEC-D 治疗的患者。TC 和 FEC-D 无 G-CSF 治疗 FN 发生率的汇总随机效应荟萃分析估计值分别为 29%(95%CI 24-35%)和 31%(95%CI 27-35%),G-CSF 可分别降低 76%(RR=0.24,95%CI 0.14-0.41)和 63%(RR=0.37,95%CI 0.11-1.24)的相对风险。

结论

在常规临床实践中,无 G-CSF 的 TC 和 FEC-D 与 FN 发生率超过了普遍推荐使用初级 G-CSF 预防的 20%阈值,且明显高于关键临床试验报告的发生率。

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