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Bendamustine as first-line treatment in patients with advanced indolent non-Hodgkin lymphoma and mantle cell lymphoma in German routine clinical practice

机译:苯达莫司汀作为晚期惰性非霍奇金淋巴瘤和套细胞淋巴瘤的一线治疗在德国的常规临床实践中

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摘要

Bendamustine has demonstrated clinical activity and a favorable safety profile as monotherapy or in combination with rituximab in lymphoid malignancies. As interventional trials do not always reflect clinical reality, we were interested in the treatment modalities and the outcome of bendamustine-based first-line therapy in patients with advanced indolent non-Hodgkin lymphoma (NHL) and mantle cell lymphoma (MCL) in routine practice. Between April 2010 and October 2011, 324 patients were enrolled in a prospective non-interventional multicenter study. Choice of the bendamustine regimen was at the treating physician’s discretion. Effectiveness was assessed by best response. Mean age at onset of therapy was 69 years. The majority (94 %) of the patients was treated with bendamustine in combination with rituximab at a median bendamustine dose of 177 mg/m2 per cycle. Most often, bendamustine was administered on days 1 and 2 (87 %) at 4-week intervals over a median of 6 cycles. Two hundred eighty-one patients qualified for evaluation of response. The overall response rate was 86 % (complete response 43 %, partial response 43 %, stable disease 10 %, progressive disease 4 %). Side effects of all grades were documented for 161 of the 323 patients (50 %), most frequently affecting blood/bone marrow (35 %). Fifty-four (17 %) patients experienced side effects of grade 3 (15 %) or grade 4 (2 %), and two patients grade 5 toxicities. Bendamustine-based first-line treatment of patients with advanced indolent NHL and MCL in clinical routine practice was assessed as effective and well tolerated in our study. Response was comparable to results from interventional clinical trials.
机译:苯达莫司汀已证明在淋巴恶性肿瘤中作为单一疗法或与利妥昔单抗联用具有临床活性和良好的安全性。由于介入试验并不总是能反映临床现实,因此我们对常规治疗中晚期惰性非霍奇金淋巴瘤(NHL)和套细胞淋巴瘤(MCL)患者基于苯达莫司汀的一线治疗的治疗方式和结果感兴趣。在2010年4月至2011年10月之间,有324名患者参加了一项前瞻性非干预性多中心研究。苯达莫司汀治疗方案的选择由主治医师决定。通过最佳反应评估效果。开始治疗的平均年龄为69岁。大多数患者(94%)接受苯达莫司汀联合利妥昔单抗治疗,苯达莫司汀的平均剂量为每个周期177 mg / m 2 。最常见的是,苯达莫司汀在第1天和第2天(87%)以4周为间隔的6个周期的中位数给药。 281位患者符合评估反应的条件。总体缓解率为86%(完全缓解43%,部分缓解43%,稳定疾病10%,进行性疾病4%)。记录了323名患者中的161名(50%)的所有等级的副作用,最常影响血液/骨髓(35%)。五十四(17%)名患者出现3级(15%)或4级(2%)的副作用,还有2名5级毒性反应的患者。在临床常规实践中,以苯达莫司汀为基础的晚期惰性NHL和MCL患者的一线治疗在我们的研究中被评估为有效且耐受性良好。反应与介入临床试验的结果相当。

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