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本文引用的文献

1
Myeloid growth factors.髓系生长因子
J Natl Compr Canc Netw. 2011 Aug 1;9(8):914-32. doi: 10.6004/jnccn.2011.0075.
2
Intense dose-dense sequential chemotherapy with epirubicin, paclitaxel, and cyclophosphamide compared with conventionally scheduled chemotherapy in high-risk primary breast cancer: mature results of an AGO phase III study.密集剂量序贯化疗联合表柔比星、紫杉醇和环磷酰胺与高危原发性乳腺癌常规化疗方案的比较:AGO Ⅲ期研究的成熟结果。
J Clin Oncol. 2010 Jun 10;28(17):2874-80. doi: 10.1200/JCO.2009.24.7643. Epub 2010 May 10.
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Acute myeloid leukemia or myelodysplastic syndrome in randomized controlled clinical trials of cancer chemotherapy with granulocyte colony-stimulating factor: a systematic review.粒细胞集落刺激因子在癌症化疗随机对照临床试验中治疗急性髓细胞白血病或骨髓增生异常综合征的系统评价。
J Clin Oncol. 2010 Jun 10;28(17):2914-24. doi: 10.1200/JCO.2009.25.8723. Epub 2010 Apr 12.
4
Cyclophosphamide, epirubicin, and Fluorouracil versus dose-dense epirubicin and cyclophosphamide followed by Paclitaxel versus Doxorubicin and cyclophosphamide followed by Paclitaxel in node-positive or high-risk node-negative breast cancer.环磷酰胺、表柔比星和氟尿嘧啶与密集型表柔比星和环磷酰胺序贯紫杉醇与多柔比星和环磷酰胺序贯紫杉醇治疗淋巴结阳性或高危淋巴结阴性乳腺癌的比较。
J Clin Oncol. 2010 Jan 1;28(1):77-82. doi: 10.1200/JCO.2009.22.1077. Epub 2009 Nov 9.
5
Pegfilgrastim primary prophylaxis vs. current practice neutropenia management in elderly breast cancer patients receiving chemotherapy.培非格司亭初级预防与老年乳腺癌患者化疗中性粒细胞减少症管理的现行实践。
Crit Rev Oncol Hematol. 2010 Jun;74(3):203-10. doi: 10.1016/j.critrevonc.2009.06.004. Epub 2009 Sep 11.
6
Efficacy of sequential high-dose doxorubicin and ifosfamide compared with standard-dose doxorubicin in patients with advanced soft tissue sarcoma: an open-label randomized phase II study of the Spanish group for research on sarcomas.序贯高剂量阿霉素与异环磷酰胺对比标准剂量阿霉素治疗晚期软组织肉瘤患者的疗效:西班牙肉瘤研究小组的一项开放标签随机II期研究
J Clin Oncol. 2009 Apr 10;27(11):1893-8. doi: 10.1200/JCO.2008.19.2930. Epub 2009 Mar 9.
7
Impact of primary prophylaxis with granulocyte colony-stimulating factor on febrile neutropenia and mortality in adult cancer patients receiving chemotherapy: a systematic review.粒细胞集落刺激因子一级预防对接受化疗的成年癌症患者发热性中性粒细胞减少症及死亡率的影响:一项系统评价
J Clin Oncol. 2007 Jul 20;25(21):3158-67. doi: 10.1200/JCO.2006.08.8823.
8
2006 update of recommendations for the use of white blood cell growth factors: an evidence-based clinical practice guideline.白细胞生长因子使用建议的2006年更新:基于证据的临床实践指南
J Clin Oncol. 2006 Jul 1;24(19):3187-205. doi: 10.1200/JCO.2006.06.4451. Epub 2006 May 8.
9
Two-weekly or 3-weekly CHOP chemotherapy with or without etoposide for the treatment of elderly patients with aggressive lymphomas: results of the NHL-B2 trial of the DSHNHL.每两周或每三周进行一次CHOP化疗(加或不加依托泊苷)用于治疗老年侵袭性淋巴瘤患者:德国淋巴瘤研究组(DSHNHL)的NHL-B2试验结果
Blood. 2004 Aug 1;104(3):634-41. doi: 10.1182/blood-2003-06-2095. Epub 2004 Mar 11.
10
Measuring inconsistency in meta-analyses.评估荟萃分析中的异质性
BMJ. 2003 Sep 6;327(7414):557-60. doi: 10.1136/bmj.327.7414.557.

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.

DOI:10.1093/annonc/mdt226
PMID:23788754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3841419/
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。