首页> 外文期刊>Gynecologic Oncology: An International Journal >Phase III trial to evaluate the efficacy of maintaining hemoglobin levels above 12.0 g/dL with erythropoietin vs above 10.0 g/dL without erythropoietin in anemic patients receiving concurrent radiation and cisplatin for cervical cancer.
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Phase III trial to evaluate the efficacy of maintaining hemoglobin levels above 12.0 g/dL with erythropoietin vs above 10.0 g/dL without erythropoietin in anemic patients receiving concurrent radiation and cisplatin for cervical cancer.

机译:III期临床试验旨在评估在接受放射线和顺铂联合治疗的贫血宫颈癌患者中,使用促红细胞生成素维持血红蛋白水平高于12.0 g / dL而不使用促红细胞生成素维持高于10.0 g / dL的疗效。

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PURPOSE: To determine whether maintaining HGB levels > or = 12.0 g/dL with recombinant human erythropoietin (R-HUEPO) compared to "standard" treatment (transfusion for HGB < or = 10.0 g/dL) improves progression-free survival (PFS), overall survival (OS) and local control (LC) in women receiving concurrent weekly cisplatin and radiation (CT/RT) for carcinoma of the cervix. In addition, to determine whether platinum-DNA adducts were associated with clinical characteristics or outcome. METHODS: Patients with stage IIB-IVA cervical cancer and HGB < 14.0 g/dL were randomly assigned to CT/RT+/-R-HUEPO (40,000 units s.c. weekly). R-HUEPO was stopped if HGB > 14.0 g/dL. Endpoints were PFS, OS and LC. Platinum-DNA adducts were quantified using immunocytochemistry assay in buccal cells. RESULTS: Between 08/01 and 09/03, 109 of 114 patients accrued were eligible. Fifty-two received CT/RT and 57 CT/RT+R-HUEPO. The study closed prematurely, with less than 25% of the planned accrual, due to potential concerns for thromboembolic event (TE) with R-HUEPO. Median follow-up was 37 months (range 9.8-50.4 months). PFS and OS at 3 years should be 65% and 75% for CT/RT and 58% and 61% for CT/RT+R-HUEPO, respectively. TE occurred in 4/52 receiving CT/RT and 11/57 with CT/RT+R-HUEPO, not all considered treatment related. No deaths occurred from TE. High-platinum adducts were associated with inferior PFS and LC. CONCLUSION: TE is common in cervical cancer patients receiving CT/RT. Difference in TE rate between the two treatments was not statistically significant. The impact of maintaining HGB level > 12.0 g/dL on PFS, OS and LC remains undetermined.
机译:目的:确定与“标准”治疗(输注HGB <或= 10.0 g / dL)相比,重组人促红细胞生成素(R-HUEPO)维持HGB水平>或= 12.0 g / dL是否可改善无进展生存期(PFS)接受每周同时顺铂和放疗(CT / RT)治疗宫颈癌的妇女的总生存期(OS)和局部控制(LC)。此外,确定铂-DNA加合物是否与临床特征或预后相关。方法:将IIB-IVA期宫颈癌且HGB <14.0 g / dL的患者随机分配至CT / RT +/- R-HUEPO(每周40,000单位皮下注射)。如果HGB> 14.0 g / dL,则停止R-HUEPO。端点是PFS,OS和LC。使用颊细胞中的免疫细胞化学测定法定量铂-DNA加合物。结果:在08/01和09/03之间,在114名患者中有109名符合条件。 52例接受了CT / RT,57例接受了CT / RT + R-HUEPO。由于可能担心R-HUEPO对血栓栓塞事件(TE)的影响,该研究过早结束,不到计划应计项目的25%。中位随访时间为37个月(9.8-50.4个月)。对于CT / RT,3年时的PFS和OS应分别为65%和75%,对于CT / RT + R-HUEPO,应分别为58%和61%。 TE发生在接受CT / RT的4/52和接受CT / RT + R-HUEPO的11/57中,并非所有患者都认为与治疗相关。 TE没有造成死亡。高铂加合物与劣质PFS和LC有关。结论:TE在接受CT / RT的宫颈癌患者中很常见。两种治疗之间的TE率差异无统计学意义。维持HGB> 12.0 g / dL对PFS,OS和LC的影响尚不确定。

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