Department of Hematology, Centre Hospitalier Universitaire de Rennes, Rennes.
Ann Oncol. 2012 Jun;23(6):1555-61. doi: 10.1093/annonc/mdr450. Epub 2011 Oct 19.
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 between 65 and 80 years of age with newly diagnosed MCL received up to six cycles of RiPAD+C.
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.
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.
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。
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。
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。
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。