Fenk Roland, Michael Mark, Zohren Fabian, Graef Thorsten, Czibere Akos, Bruns Ingmar, Neumann Frank, Fenk Barbara, Haas Rainer, Kobbe Guido
Department of Haematology, Oncology and Clinical Immunology, Heinrich-Heine University, Duesseldorf, Germany.
Leuk Lymphoma. 2007 Dec;48(12):2345-51. doi: 10.1080/10428190701694194.
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.
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。