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Efficacy of bendamustine and rituximab as first salvage treatment in chronic lymphocytic leukemia and indirect comparison with ibrutinib: a GIMEMA ERIC and UK CLL FORUM study

机译:苯达莫司汀和利妥昔单抗作为慢性淋巴细胞白血病的首次抢救治疗的功效以及与依鲁替尼的间接比较:GIMEMAERIC和UK CLL FORUM研究

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摘要

We performed an observational study on the efficacy of ben-damustine and rituximab (BR) as first salvage regimen in chronic lymphocytic leukemia (CLL). In an intention-to-treat analysis including 237 patients, the median progression-free survival (PFS) was 25 months. The presence of del(17p), unmutated IGHV and advanced stage were associated with a shorter PFS at multivariate analysis. The median time-to-next treatment was 31.3 months. Front-line treatment with a chemoimmunotherapy regimen was the only predictive factor for a shorter time to next treatment at multivariate analysis. The median overall survival (OS) was 74.5 months. Advanced disease stage (i.e. Rai stage III-IV or Binet stage C) and resistant disease were the only parameters significantly associated with a shorter OS. Grade 3-5 infections were recorded in 6.3% of patients. A matched-adjusted indirect comparison with ibrutinib given second-line within Named Patient Programs in the United Kingdom and in Italy was carried out with OS as objective end point. When restricting the analysis to patients with intact 17p who had received chemoimmunotherapy in first line, there was no difference in OS between patients treated with ibrutinib (63% alive at 36 months) and patients treated with BR (74.4% alive at 36 months). BR is an efficacious first salvage regimen in CLL in a real-life population, including the elderly and unfit patients. BR and ibrutinib may be equally effective in terms of OS when used as first salvage treatment in patients without 17p deletion.
机译:我们对苯达莫司汀和利妥昔单抗(BR)作为慢性淋巴细胞白血病(CLL)的首个挽救方案的疗效进行了观察性研究。在包括237例患者的意向性治疗分析中,中位无进展生存期(PFS)为25个月。在多变量分析中,del(17p),未突变的IGHV和晚期的存在与较短的PFS相关。下次治疗的中位时间为31.3个月。在多变量分析中,化学免疫疗法方案的一线治疗是缩短下次治疗时间的唯一预测因素。中位总生存期(OS)为74.5个月。晚期疾病阶段(即Rai III-IV阶段或Binet C阶段)和耐药性疾病是与较短OS显着相关的唯一参数。在6.3%的患者中记录了3-5级感染。以OS为目标终点,在英国和意大利的指定患者计划中,与依鲁替尼给予二线的患者进行了匹配调整后的间接比较。将分析仅限于一线接受化学免疫疗法的17p完整患者时,接受依鲁替尼治疗的患者(36个月存活率63%)和接受BR治疗的患者(36个月的存活率74.4%)之间的OS无差异。 BR是包括老年人和身体不适患者在内的现实生活中CLL的一种有效的抢救方案。在没有17p缺失的患者中,BR和依鲁替尼作为OS的首次抢救治疗时,在OS方面可能同样有效。

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