Hôpital Européen Georges Pompidou, AP-HP, Paris, France.
Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
Eur Respir J. 2018 Oct 4;52(4). doi: 10.1183/13993003.01220-2018. Print 2018 Oct.
The anti-tumour and anti-metastatic properties of heparins have not been tested in patients with early stage cancer. Whether adjuvant low molecular weight heparin (LMWH) tinzaparin impacts the survival of patients with resected non-small cell lung cancer (NSCLC) was investigated.Patients with completely resected stage I, II or IIIA NSCLC were randomly allocated to receive subcutaneous tinzaparin 100 IU·kg once a day for 12 weeks or no treatment in addition to standard of care. The trial was open-label with blinded central adjudication of study outcomes. The primary outcome was overall survival.In 549 patients randomised to tinzaparin (n=269) or control (n=280), mean±sd age was 61.6±8.9 years, 190 (34.6%) patients had stage II-III disease, and 220 (40.1%) patients received adjuvant chemotherapy. Median follow-up was 5.7 years. There was no significant difference in overall survival between groups (hazard ratio (HR) 1.24, 95% CI 0.92-1.68; p=0.17). There was no difference in the cumulative incidence of recurrence between groups (subdistribution HR 0.94, 95% CI 0.68-1.30; p=0.70).Adjuvant tinzaparin had no detectable impact on overall and recurrence-free survival of patients with completely resected stage I-IIIA NSCLC. These results do not support further clinical evaluation of LMWHs as anti-tumour agents.
肝素的抗肿瘤和抗转移特性尚未在早期癌症患者中进行过测试。研究了辅助低分子量肝素(LMWH)亭扎肝素是否会影响接受完全切除的非小细胞肺癌(NSCLC)患者的生存。
完全切除的 I 期、II 期或 IIIA 期 NSCLC 患者被随机分配接受皮下亭扎肝素 100 IU·kg 每天一次,持续 12 周,或在标准治疗基础上加用安慰剂。试验是开放性的,研究结果由中央盲法裁决。主要结局是总生存期。
在 549 名随机分配至亭扎肝素(n=269)或对照组(n=280)的患者中,平均年龄±标准差为 61.6±8.9 岁,190(34.6%)例患者为 II-III 期疾病,220(40.1%)例患者接受辅助化疗。中位随访时间为 5.7 年。两组患者的总生存期无显著差异(风险比(HR)1.24,95%CI 0.92-1.68;p=0.17)。两组间复发的累积发生率无差异(亚分布 HR 0.94,95%CI 0.68-1.30;p=0.70)。
辅助亭扎肝素对完全切除的 I-IIIA 期 NSCLC 患者的总生存期和无复发生存期没有明显影响。这些结果不支持进一步临床评估 LMWH 作为抗肿瘤药物。