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硼替佐米、地塞米松和苯达莫司汀用于复发或难治性多发性骨髓瘤患者的递增疗法。

Escalation therapy with bortezomib, dexamethasone and bendamustine for patients with relapsed or refractory multiple myeloma.

作者信息

Fenk Roland, Michael Mark, Zohren Fabian, Graef Thorsten, Czibere Akos, Bruns Ingmar, Neumann Frank, Fenk Barbara, Haas Rainer, Kobbe Guido

机构信息

Department of Haematology, Oncology and Clinical Immunology, Heinrich-Heine University, Duesseldorf, Germany.

出版信息

Leuk Lymphoma. 2007 Dec;48(12):2345-51. doi: 10.1080/10428190701694194.

Abstract

In order to improve remission rates without causing undue toxicity, we treated 50 patients with relapsed/refractory multiple myeloma according to an institutional sequential treatment algorithm. Bortezomib was given as monotherapy (1.3 mg/m(2) on day 1 + 4 + 8 + 11) followed by the addition of dexamethasone in a first (40 mg on day 1 + 4 + 8 + 11) and bendamustine (50 - 100 mg/m(2) on day 1 + 8) in a second escalation step for patients with less than a minor response. Bortezomib monotherapy was sufficient in 23 (46%) patients, treatment escalation with dexamethasone was necessary in 20 (40%) patients and 7 (14%) patients needed triple combination therapy. Overall response rate was 84% while toxicity was manageable. Median time to progression and overall survival were 8 and 20 months, respectively. In conclusion, this treatment algorithm resulted in responses in the majority of heavily pre-treated patients while at the same time restricting the toxicity of triple combination therapy to only 14% of non-responding patients.

摘要

为了在不引起过度毒性的情况下提高缓解率,我们根据机构的序贯治疗方案对50例复发/难治性多发性骨髓瘤患者进行了治疗。硼替佐米作为单一疗法给药(第1、4、8和11天给予1.3mg/m²),对于反应欠佳的患者,首先加用地塞米松(第1、4、8和11天给予40mg),在第二个升级步骤中加用苯达莫司汀(第1和8天给予50 - 100mg/m²)。23例(46%)患者仅使用硼替佐米单一疗法就足够了,20例(40%)患者需要加用地塞米松进行治疗升级,7例(14%)患者需要三联联合治疗。总体缓解率为84%,毒性可控。中位进展时间和总生存期分别为8个月和20个月。总之,这种治疗方案在大多数经过大量前期治疗的患者中产生了反应,同时将三联联合治疗的毒性限制在仅14%的无反应患者中。

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