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来那度胺、硼替佐米、多柔比星、地塞米松和苯丁酸氮芥(RiPAD+C)联合方案作为老年套细胞淋巴瘤患者一线治疗:GOELAMS Ⅱ期试验结果。

Combination of rituximab, bortezomib, doxorubicin, dexamethasone and chlorambucil (RiPAD+C) as first-line therapy for elderly mantle cell lymphoma patients: results of a phase II trial from the GOELAMS.

机构信息

Department of Hematology, Centre Hospitalier Universitaire de Rennes, Rennes.

出版信息

Ann Oncol. 2012 Jun;23(6):1555-61. doi: 10.1093/annonc/mdr450. Epub 2011 Oct 19.

Abstract

BACKGROUND

There is no consensual first-line chemotherapy for elderly patients with mantle cell lymphoma (MCL). The GOELAMS (Groupe Ouest-Est des Leucémies Aiguës et Maladies du Sang) group previously developed the (R)VAD+C regimen (rituximab, vincristine, doxorubicin, dexamethasone and chlorambucil), which appeared as efficient as R-CHOP (rituximab, cyclophosphamide, doxorubicine, vincristine, prednisone) while less toxic. Based on this protocol, we now added bortezomib (RiPAD+C: rituximab, bortezomib, doxorubicin, dexamethasone and chlorambucil) given its efficacy in relapsed/refractory MCL patients. The goal of the current phase II trial was to evaluate the feasibility and efficacy of the RiPAD+C regimen as frontline therapy for elderly patients with MCL.

PATIENTS AND METHODS

Patients between 65 and 80 years of age with newly diagnosed MCL received up to six cycles of RiPAD+C.

RESULTS

Thirty-nine patients were enrolled. Median age was 72 years (65-80). After four cycles of RiPAD+C, the overall response rate was 79%, including 51% complete responses (CRs). After six cycles, CR rate increased up to 59%. After a 27-month follow-up, median progression-free survival (PFS) is 26 months and median overall survival has not been reached. Four patients (10%) discontinued the treatment because of a severe toxicity and seven patients (18%) experienced grade 3 neurotoxicity.

CONCLUSION

The bortezomib-containing RiPAD+C regimen results in high CR rates and prolonged PFS with predictable and manageable toxic effects in elderly patients with MCL.

摘要

背景

对于老年套细胞淋巴瘤(MCL)患者,目前尚无共识的一线化疗方案。GOELAMS(法国东部和西部急性白血病和血液疾病小组)曾开发过(R)VAD+C 方案(利妥昔单抗、长春新碱、多柔比星、地塞米松和苯丁酸氮芥),该方案与 R-CHOP(利妥昔单抗、环磷酰胺、多柔比星、长春新碱、泼尼松)相比疗效相当,但毒性更小。在此方案基础上,我们加入硼替佐米(RiPAD+C:利妥昔单抗、硼替佐米、多柔比星、地塞米松和苯丁酸氮芥),因其在复发/难治性 MCL 患者中的疗效而使用。本 II 期试验的目的是评估 RiPAD+C 方案作为老年 MCL 患者一线治疗的可行性和疗效。

患者和方法

新诊断为 MCL 的年龄在 65 至 80 岁之间的患者接受了最多 6 个周期的 RiPAD+C 治疗。

结果

共纳入 39 例患者。中位年龄为 72 岁(65-80 岁)。在接受 4 个周期的 RiPAD+C 后,总体缓解率为 79%,包括 51%的完全缓解(CR)。在 6 个周期后,CR 率增加至 59%。在 27 个月的随访后,中位无进展生存期(PFS)为 26 个月,中位总生存期尚未达到。4 例患者(10%)因严重毒性而停止治疗,7 例患者(18%)出现 3 级神经毒性。

结论

含硼替佐米的 RiPAD+C 方案在老年 MCL 患者中可产生高 CR 率、延长 PFS,并具有可预测和可控的毒性作用。

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