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首页> 外文期刊>Acta Haematologica >Efficacy of Gemcitabine as Salvage Therapy for Relapsed and Refractory Aggressive Non-Hodgkin Lymphoma
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Efficacy of Gemcitabine as Salvage Therapy for Relapsed and Refractory Aggressive Non-Hodgkin Lymphoma

机译:吉西他滨作为复发和难治性侵袭性非霍奇金淋巴瘤的救人疗法的疗效

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摘要

Gemcitabine-based salvage therapy is considered an effective treatment for relapsed and refractory Non-Hodgkin's lymphoma (NHL), We analyzed the outcome of 41 consecutive NHL patients treated with gemcitabine-based regimens between January 2007 and October 2015. Twenty-eight males and 13 females (median age 66.4 years) were included. The median follow-up from gemcitabine initiation was 7.3 months. Thirty patients (73%) had B-cell, and eleven (27%) had T-cell, lymphoma. All patients received a median of 2 prior regimens, of which at least 1 was anthracycline based, Twenty-eight patients (78%) received full-dose while 9 (22%) received reduced-dose regimens. The overall response rate was 37%, with 24% (n = 10) complete response, 12% (n = 5) partial response, and 63% (n = 22) progressive disease or stable disease, The median progression-free survival (PFS) was 47 days (range 12-1,318), the median overall survival (OS) was 1,9 years. Twenty patients (49%) died during follow-up. Grade 3-4 hematological toxicity was reported in 21 patients (51%). Relapsed vs. refractory disease, as well as a response to gemcitabine, predicted better PFS and OS, Use of a full-dose regimen predicted a better OS. Compared to previously published data, we observed less favorable outcomes, The administration of gemcitabine-based therapy as a salvage regimen for patients with relapsed or refractory NHL had limited success. Innovative therapies for these patients are an unmet need. (C) 2019 S. Karger AG, Basel
机译:基于吉西他滨的挽救疗法被认为是对复发和难治性非霍奇金淋巴瘤(NHL)的有效治疗方法,我们分析了2007年1月至2015年1月至10月的基于吉西他滨的方案治疗的41名连续NHL患者的结果。二十八名男性和13名包括女性(中位数66.4岁)。从吉西他滨开始的中位随访时间为7.3个月。 30名患者(73%)具有B细胞,11(27%)具有T细胞,淋巴瘤。所有患者均接受了2个先前的中位数的中位数,其中至少1个是蒽环类胰岛素的基础,28名患者(78%)接受全剂量,而9(22%)接受减少剂量的减少剂量方案。整体反应率为37%,24%(n = 10)完全响应,12%(n = 5)部分反应,63%(n = 22)渐进性疾病,中位进展生存( PFS)为47天(范围为12-1,318),中位数总生存(OS)为1,9岁。在随访期间死亡二十名患者(49%)。 21例患者报告了3-4级血液学毒性(51%)。复发与耐火性疾病,以及对吉西他滨的反应,预测更好的PFS和OS,使用全剂量方案预测更好的操作系统。与先前公布的数据相比,我们观察到不太有利的结果,吉西他滨的疗法作为复发或难治性NHL患者的救助方案的成功有限。这些患者的创新疗法是一个未满足的需求。 (c)2019年S. Karger AG,巴塞尔

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