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首页> 外文期刊>Clinical lymphoma, myeloma & leukemia >Bortezomib (velcade), rituximab, cyclophosphamide, and dexamethasone combination regimen is active as front-line therapy of low-grade non-hodgkin lymphoma
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Bortezomib (velcade), rituximab, cyclophosphamide, and dexamethasone combination regimen is active as front-line therapy of low-grade non-hodgkin lymphoma

机译:硼替佐米(velcade),利妥昔单抗,环磷酰胺和地塞米松联合方案可作为低度非霍奇金淋巴瘤的一线治疗

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Objective: To evaluate the efficacy and toxicity of the combination of VRCD (velcade/rituximab/cyclophosphamide/dexamethasone) in chemotherapy-nave low-grade non-Hodgkin lymphoma or patients with transplantation-ineligible mantle cells. Methods: The patients were treated with velcade, at 1.6 mg/m 2, on days 1, 8, 15, and 22 on every 35-day cycle. Rituximab was given at 375 mg/m 2 on the same days as velcade during cycle 1 and then only on day 1 in subsequent cycles. Dexamethasone was given orally at 40 mg on days 1, 2, 8, 9, 15, 16, 22, and 23. Cyclophosphamide was administered orally at 400 mg/m 2 on days 1-4. The patients had to meet criteria to initiate therapy and had to demonstrate adequate performance status and organ function. Results: Twelve patients were enrolled, after which the study was closed due to a lack of funding. The median age was 68 years (37-83 years), with 83% having stage III/IV disease. Five patients had marginal zone, 4 had follicular, 2 had small lymphocytic, and 1 had mantle cell histologies. The overall response rate was 90% (complete response, 54%). At a median follow-up of 22 months, 9 (75%) patients remain alive, and the median time to progression has not been reached. A third of the patients required dose reductions after a median of 6.5 cycles. No grade 3 or 4 peripheral neuropathy was witnessed. Conclusions: Although the number of studied patients is small, VRCD appears safe and active as front-line therapy for low-grade non-Hodgkin lymphoma. Further studies are justified.
机译:目的:评价VRCD(velcade /利妥昔单抗/环磷酰胺/地塞米松)联合治疗对化疗敏感的低度非霍奇金淋巴瘤或不适合移植的套细胞患者的疗效和毒性。方法:在每35天周期的第1、8、15和22天,以1.6 mg / m 2的Velcade对其进行治疗。在周期1的velcade的同一天,给予利妥昔单抗375 mg / m 2,随后的周期仅在第1天给予利妥昔单抗。在第1、2、8、9、15、16、22和23天口服地塞米松40 mg,在第1-4天以400 mg / m 2口服环磷酰胺。患者必须符合开始治疗的标准,并且必须表现出足够的机能状态和器官功能。结果:招募了12名患者,此后由于缺乏资金而关闭了研究。中位年龄为68岁(37-83岁),其中83%患有III / IV期疾病。边缘区5例,滤泡4例,小淋巴细胞2例,套细胞组织学1例。总体缓解率为90%(完全缓解率为54%)。在22个月的中位随访中,有9名(75%)患者仍然存活,并且尚未达到进展的中位时间。中位数6.5个周期后,三分之一的患者需要降低剂量。没有观察到3或4级周围神经病变。结论:尽管研究的患者人数很少,但VRCD似乎是安全且有效的低级非霍奇金淋巴瘤一线治疗药物。进一步的研究是合理的。

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