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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Bendamustin-Rituximab Combination Is a Safe and Effective, Ambulatory Treatment for Elderly Patients with Chronic Lymphocytic Leukemia: Retrospective Real-world Analysis by Age from a German Registry and Review of the Literature
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Bendamustin-Rituximab Combination Is a Safe and Effective, Ambulatory Treatment for Elderly Patients with Chronic Lymphocytic Leukemia: Retrospective Real-world Analysis by Age from a German Registry and Review of the Literature

机译:苯达莫司汀-利妥昔单抗联合治疗老年慢性淋巴细胞白血病的安全,有效,门诊治疗:来自德国登记处的年龄回顾性现实世界分析和文献综述

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Background: Treatment recommendations in chronic lymphocytic leukemia (CLL) are based upon selected, otherwise healthy study populations mostly under 72 years of age. The Project group Internistic Oncology (PIO) embarked on an analysis of the 'real-world' safety and efficacy of bendamustine with and without rituximab in unselected outpatients. Patients and Methods: A multicenter, open-label, prospectively stratified, retrospective study was conducted to determine routine feasibility, toxicity, and response rates obtained by bendamustine with and without rituximab in a random population of mostly elderly patients with CLL. Records were obtained from 775 patients with CLL from 60 private medical oncology practices. Informed consent was obtained prior to study participation. The median observation time was 28 months. Patients were stratified according to age, and treatment. Response criteria and statistics followed international guidelines adopted by the "German Chronic Lymphocytic Leukemia Study Group". Results: Overall, 57.5% of patients were over 70 (range=36-95) years old. Eastern Cooperative Oncology Group performance status and age influenced the total dose given, decreasing by 20% between ECOG 0 and 3, and by 15% above 80 years old. Response rates did not differ between the ages of 60 to 80 years, with an overall remission rate for bendamustine of 83%, and for the combination therapy of 89%, decreasing above the age of 80 years. Febrile neutropenia occurred in 25% of 775 patients, and grade 3 or 4 non-hematological adverse events in 9.55% (n=74), not interfering with the treatment. Conclusion: Bendamustine with and without rituximab was associated with high activity and tolerability, irrespective of age and risk factors. The median overall survival was 64 months with a 3-year survival rate of 72%; progression-free survival was 30.6 months, and the 3 year PFS was 43%. The good tolerability and feasibility of bendamustine with and without rituximab, in particular for the elderly population with CLL argues for it being a safe outpatient treatment.
机译:背景:慢性淋巴细胞性白血病(CLL)的治疗建议是基于选定的,否则为健康研究人群的,这些人群大多在72岁以下。项目小组内部肿瘤学(PIO)开始对未经选择的门诊患者使用和不使用利妥昔单抗的苯达莫司汀的“现实”安全性和有效性进行分析。患者和方法:进行了一项多中心,开放标签,前瞻性分层的回顾性研究,以确定在大多数年龄较大的CLL患者的随机人群中,苯达莫司汀联合或不联合利妥昔单抗获得的常规可行性,毒性和反应率。从60种私人医学肿瘤实践中获得了775名CLL患者的记录。在参加研究之前获得知情同意。中位观察时间为28个月。根据年龄和治疗对患者进行分层。反应标准和统计学遵循“德国慢性淋巴细胞白血病研究小组”通过的国际准则。结果:总体上,有57.5%的患者年龄超过70岁(范围= 36-95)。东部合作肿瘤小组的表现状况和年龄影响了给予的总剂量,在ECOG 0和3之间下降了20%,在80岁以上下降了15%。在60到80岁之间,缓解率没有差异,苯达莫司汀的总体缓解率是83%,联合治疗的总体缓解率是89%,在80岁以上时降低。在775例患者中,有25%出现发热性中性粒细胞减少,在9.55%(n = 74)中发生3或4级非血液学不良事件,不干扰治疗。结论:苯达莫司汀联合和不联合利妥昔单抗均具有较高的活性和耐受性,而与年龄和危险因素无关。中位总生存期为64个月,三年生存率为72%。无进展生存期为30.6个月,而3年PFS为43%。含有和不含利妥昔单抗的苯达莫司汀的良好耐受性和可行性,特别是对于CLL的老年人群,认为这是一种安全的门诊治疗方法。

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