Thrombosis Research Institute, London, UK.
J Thromb Haemost. 2010 Jun;8(6):1223-9. doi: 10.1111/j.1538-7836.2010.03892.x. Epub 2010 Apr 30.
There is not enough clinical evidence to make a strong recommendation on the optimal duration of thromboprophylaxis using low-molecular weight heparins (LMWH) in patients undergoing major cancer surgery.
CANBESURE is a randomized, double-blind study which enrolled patients admitted for abdominal or pelvic surgery for cancer. They received 3500 IU of bemiparin subcutaneously once daily for 8 days and were then randomized to receive either bemiparin or placebo for 20 additional days. Bilateral venography was performed after 20 days and evaluated blinded. The primary efficacy outcome was the composite of deep vein thrombosis (DVT), non-fatal pulmonary embolism (PE) and all-cause mortality at the end of double-blind period. Major venous thromboembolism (proximal deep-vein thrombosis, non-fatal pulmonary embolism and venous thromboembolism-related deaths) was also evaluated. The primary safety outcome was major bleeding.
Six hundred and twenty-five and 488 patients were included in the safety and main efficacy analyzes, respectively. The primary efficacy outcome occurred in 25 out of 248 patients (10.1%) in the bemiparin group and 32 out of 240 (13.3%) in the placebo group (relative risk reduction 24.4%; 95% CI: -23.7-53.8%; P = 0.26). At the end of double-blind period, major venous thromboembolism occurred in 2 (0.8%) and 11 (4.6%) patients, respectively (relative risk reduction 82.4%; 95% CI: 21.5-96.1%; P = 0.010). No significant difference was found in major bleedings.
Four weeks compared with 1 week of prophylaxis with bemiparin after abdominal or pelvic cancer surgery did not significantly reduce the primary efficacy outcome, but decreased major venous thromboembolism (VTE) without increasing hemorrhagic complications.
目前尚无足够的临床证据可以对使用低分子肝素(LMWH)进行大手术癌症患者的最佳血栓预防时间做出强有力的推荐。
CANBESURE 是一项随机、双盲研究,纳入了因腹部或盆腔癌症手术入院的患者。他们每天接受 3500IU 的贝米肝素皮下注射,持续 8 天,然后随机接受贝米肝素或安慰剂治疗 20 天。20 天后进行双侧静脉造影,并进行盲法评估。主要疗效终点为双盲期结束时深静脉血栓形成(DVT)、非致命性肺栓塞(PE)和全因死亡率的复合事件。还评估了主要静脉血栓栓塞事件(近端深静脉血栓形成、非致命性肺栓塞和与静脉血栓栓塞相关的死亡)。主要安全性终点为大出血。
625 例和 488 例患者分别纳入安全性和主要疗效分析。贝米肝素组 248 例患者中有 25 例(10.1%)和安慰剂组 240 例患者中有 32 例(13.3%)发生主要疗效终点事件(相对风险降低 24.4%;95%CI:-23.7 至 53.8%;P = 0.26)。双盲期结束时,主要静脉血栓栓塞事件分别发生在 2 例(0.8%)和 11 例(4.6%)患者中(相对风险降低 82.4%;95%CI:21.5 至 96.1%;P = 0.010)。大出血无显著差异。
与腹部或盆腔癌症手术后 1 周的预防相比,贝米肝素预防 4 周并未显著降低主要疗效终点,但降低了主要静脉血栓栓塞事件(VTE),而不增加出血并发症。