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随机 III 期临床试验:标准治疗联合低分子肝素治疗肺癌患者:FRAGMATIC 试验。

Randomized Phase III Trial of Standard Therapy Plus Low Molecular Weight Heparin in Patients With Lung Cancer: FRAGMATIC Trial.

机构信息

Fergus Macbeth, Jessica Evans, Sheikh Ahmed, and Gareth Griffiths, Wales Cancer Trials Unit; Simon Noble and Kerenza Hood, Cardiff University; David Cohen and Mirella Longo, University of South Wales; Barbara Moore, National Institute for Social Care and Health Research Clinical Research Centre, Cardiff; Gareth Griffiths, University of Southampton, Southampton; Dana Knoyle, Prince Charles Hospital, Merthyr Tydfil; Penella J. Woll, Weston Park Hospital, Sheffield; Wiebke Appel, Royal Preston Hospital, Preston; Jeanette Dickson, Mount Vernon Cancer Center, Northwood; David Ferry, Royal Wolverhampton Hospitals National Health Service Trust, Wolverhampton; Caroline Brammer, Mid Staffordshire Hospital, Stafford, United Kingdom; and Seamus Linnane, Beaumont Hospital, Dublin, Ireland.

出版信息

J Clin Oncol. 2016 Feb 10;34(5):488-94. doi: 10.1200/JCO.2015.64.0268. Epub 2015 Dec 23.

Abstract

PURPOSE

Venous thromboembolism (VTE) is common in cancer patients. Evidence has suggested that low molecular weight heparin (LMWH) might improve survival in patients with cancer by preventing both VTE and the progression of metastases. No trial in a single cancer type has been powered to demonstrate a clinically significant survival difference. The aim of this trial was to investigate this question in patients with lung cancer.

PATIENTS AND METHODS

We conducted a multicenter, open-label, randomized trial to evaluate the addition of a primary prophylactic dose of LMWH for 24 weeks to standard treatment in patients with newly diagnosed lung cancer of any stage and histology. The primary outcome was 1-year survival. Secondary outcomes included metastasis-free survival, VTE-free survival, toxicity, and quality of life.

RESULTS

For this trial, 2,202 patients were randomly assigned to the two treatment arms over 4 years. The trial did not reach its intended number of events for the primary analysis (2,047 deaths), and data were analyzed after 2,013 deaths after discussion with the independent data monitoring committee. There was no evidence of a difference in overall or metastasis-free survival between the two arms (hazard ratio [HR], 1.01; 95% CI, 0.93 to 1.10; P = .814; and HR, 0.99; 95% CI, 0.91 to 1.08; P = .864, respectively). There was a reduction in the risk of VTE from 9.7% to 5.5% (HR, 0.57; 95% CI, 0.42 to 0.79; P = .001) in the LMWH arm and no difference in major bleeding events but evidence of an increase in the composite of major and clinically relevant nonmajor bleeding in the LMWH arm.

CONCLUSION

LMWH did not improve overall survival in the patients with lung cancer in this trial. A significant reduction in VTE is associated with an increase in clinically relevant nonmajor bleeding. Strategies to target those at greatest risk of VTE are warranted.

摘要

目的

静脉血栓栓塞症(VTE)在癌症患者中很常见。有证据表明,低分子肝素(LMWH)通过预防 VTE 和转移进展,可能改善癌症患者的生存。没有一项针对单一癌症类型的试验有足够的效力来证明临床显著的生存差异。本试验旨在调查肺癌患者中的这一问题。

患者和方法

我们进行了一项多中心、开放性、随机试验,以评估在任何分期和组织学类型的新诊断肺癌患者中,在标准治疗的基础上,加用一次预防性 LMWH 剂量 24 周的效果。主要结局是 1 年生存率。次要结局包括无转移生存、无 VTE 生存、毒性和生活质量。

结果

在这项试验中,2202 名患者在 4 年内被随机分配到两个治疗组。该试验没有达到其主要分析的预期事件数量(2047 例死亡),并在与独立数据监测委员会讨论后,在 2013 例死亡后进行了数据分析。两组之间的总生存率或无转移生存率均无差异(风险比[HR],1.01;95%置信区间,0.93 至 1.10;P =.814;HR,0.99;95%置信区间,0.91 至 1.08;P =.864)。LMWH 组 VTE 的风险从 9.7%降至 5.5%(HR,0.57;95%置信区间,0.42 至 0.79;P =.001),大出血事件无差异,但 LMWH 组主要和临床相关非主要出血的复合事件有增加的证据。

结论

在这项试验中,LMWH 并未改善肺癌患者的总体生存率。VTE 的显著减少与临床相关非主要出血的增加相关。有必要针对那些有 VTE 最大风险的患者制定策略。

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