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Bortezomib as salvage treatment for heavily pretreated relapsed lymphoma patients: A multicenter retrospective study

机译:硼替佐米作为重度治疗的复发性淋巴瘤患者的挽救治疗:一项多中心回顾性研究

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Current treatments for non-Hodgkin lymphomas are not optimally effective. Among new agents, bortezomib seems to play a pivotal role in the regulation of several cell pathways involved in the development of lymphomas. After results were obtained with clinical trials, we aimed to observe treatment with bortezomib in everyday clinical practice. We performed a multicenter retrospective analysis to assess the efficacy of bortezomib in heavily pretreated (median number of previous therapies 4, range 2-6) lymphoma patients in an off-label setting. Bortezomib therapy was scheduled for 4-6 cycles (1.3mg/m2 biweekly). Data from 50 patients were collected: 22% had a complete remission, 26% obtained a partial response and the remaining 52% was non-responder. According to histotype, we observed an overall response rate (ORR) of 51.6% in mantle cell lymphomas, an ORR of 60% among follicular lymphoma patients, and an ORR of 50% in the indolent nonfollicular lymphomas. None of diffuse large B-cell lymphoma patients obtained a response. Extra-hematological toxicity was really mild, and peripheral neuropathy occurred in only 5 patients; hematological toxicity was grades 3-4 thrombocytopenia in nine patients and grades 3-4 neutropenia in only three patients. In conclusion, treatment with bortezomib as single agent resulted safe and effective in a subset of heavily pretreated lymphoma patients with usually poor outcome. New future hypotheses of investigation are indicated.
机译:非霍奇金淋巴瘤的当前治疗不是最佳的效果。在新药中,硼替佐米似乎在调节与淋巴瘤发生有关的几种细胞途径中起着关键作用。通过临床试验获得结果后,我们旨在在日常临床实践中观察使用硼替佐米的治疗。我们进行了一项多中心回顾性分析,以评估硼替佐米在标签外环境中接受大量预处理(先前治疗的中位数4,范围为2-6)的淋巴瘤患者的疗效。硼替佐米治疗计划进行4-6个周期(每两周1.3mg / m2)。收集了50例患者的数据:22%完全缓解,26%部分缓解,其余52%无反应。根据组织类型,我们观察到套细胞淋巴瘤的总缓解率为51.6%,滤泡性淋巴瘤患者的ORR为60%,惰性非滤泡性淋巴瘤的ORR为50%。弥漫性大B细胞淋巴瘤患者均未获得反应。血液学以外的毒性确实很小,只有5例患者发生了周围神经病变。 9名患者的血液学毒性为3-4级血小板减少,只有3名患者的血液学毒性为3-4级中性粒细胞减少。总之,以硼替佐米为单药治疗可在部分预治疗严重且通常结果较差的淋巴瘤患者中安全有效。指出了新的未来调查假设。

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