首页> 外文OA文献 >Response‐adapted treatment with rituximab, bendamustine, mitoxantrone, and dexamethasone followed by rituximab maintenance in patients with relapsed or refractory follicular lymphoma after first‐line immunochemotherapy: Results of the RBMDGELTAMO08 phase II trial
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Response‐adapted treatment with rituximab, bendamustine, mitoxantrone, and dexamethasone followed by rituximab maintenance in patients with relapsed or refractory follicular lymphoma after first‐line immunochemotherapy: Results of the RBMDGELTAMO08 phase II trial

机译:用Rituximab,Bendamustine,Mitoxantrone和地塞米松的响应适应治疗随后在一线免疫化疗法后复发或耐火滤饼淋巴瘤患者中的Rituximab维持:RBMDGETTAMO08期二期试验的结果

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摘要

Abstract Background Consensus is lacking regarding the optimal salvage therapy for patients with follicular lymphoma who relapse after or are refractory to immunochemotherapy. Methods This phase II trial evaluated the efficacy and safety of response‐adapted therapy with rituximab, bendamustine, mitoxantrone, and dexamethasone (RBMD) in follicular lymphoma patients who relapsed after or were refractory to first‐line immunochemotherapy. Sixty patients received three treatment cycles, and depending on their response received an additional one (complete/unconfirmed complete response) or three (partial response) cycles. Patients who responded to induction received rituximab maintenance therapy for 2 years. Results Thirty‐three (55%) and 42 (70%) patients achieved complete/unconfirmed complete response after three cycles and on completing induction therapy (4‐6 cycles), respectively (final overall response rate, 88.3%). Median progression‐free survival was 56.4 months (median follow‐up, 28.3 months; 95% CI, 15.6‐51.2). Overall survival was not reached. Progression‐free survival did not differ between patients who received four vs six cycles (P = .6665), nor between patients who did/did not receive rituximab maintenance after first‐line therapy (P = .5790). Median progression‐free survival in the 10 refractory patients was 25.5 months (95% CI, 0.6‐N/A) and was longer in patients who had shown progression of disease after 24 months of first‐line therapy (median, 56.4 months; 95% CI, 19.8‐56.4) than in those who showed early progression (median, 42.31 months; 95% CI, 24.41–NA) (P = .4258). Thirty‐six (60%) patients had grade 3/4 neutropenia. Grade 3/4 febrile neutropenia and infection were recorded during induction (4/60 [6.7%] and 5/60 [8.3%] patients, respectively) and maintenance (2/43 [4.5%] and 4/43 [9.1%] patients, respectively). Conclusions This response‐adapted treatment with RBMD followed by rituximab maintenance is an effective and well‐tolerated salvage treatment for relapsed/refractory follicular lymphoma following first‐line immunochemotherapy. Clinical trial registration ClinicalTrials.gov # NCT01133158.
机译:摘要背景缺乏对滤泡淋巴瘤患者的最佳救生疗法,缺乏毛囊淋巴瘤的患者,或者是免疫化学疗法的难治性。方法本II期试验评估了与Rituximab,Bendamustine,Mitoxantrone和地塞米松(RBMD)在复发后或难治于一线免疫化学疗法的滤泡淋巴瘤患者中的响应适应治疗的疗效和安全性。六十名患者接受了三个治疗周期,并根据他们的答复收到另外一个(完整/未经证实的完整响应)或三个(部分响应)周期。应对诱导诱导的患者接受Rituximab维持治疗2年。结果三十三(55%)和42名(70%)患者在三个循环后完成/未经证实的完全反应,分别完成诱导治疗(4-6个循环)(最终整体反应率,88.3%)。中位进展的生存率为56.4个月(28.3个月的中位随访; 95%CI,15.6-51.2)。没有达到整体生存。接受四个六个循环的患者(P = .6665)的患者之间的进展生存率并不不同(P = .6665),也不是在一线治疗后没有接受利妥昔单抗维持的患者(P = .5790)。 10名耐火患者的中位进展生存率为25.5个月(95%CI,0.6-N / A),并且在一线治疗24个月后显示疾病进展的患者(中位数,56.4个月; 95 %CI,19.8-56.4)比在展示早期进展的人(中位数,42.31个月; 95%CI,24.41-NA)(P = .4258)。 36名(60%)患者患有3/4级中性粒细胞率。在诱导过程中记录3/4级Febriere Neucopenia和感染(4/60 [6.7%]和5/60 [8.3%]患者)和维护(2/43 [4.5%]和​​4/43 [9.1%]分别为患者)。结论该响应适应的RBMD治疗随后是RITUXIMAB维持是一种有效且耐受良好的耐受性良好的拯救治疗,用于在一线免疫化学疗法后复发/难治性滤泡淋巴瘤。临床试验登记ClinicalTrials.gov#NCT01133158。

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