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利妥昔单抗、阿糖胞苷和氟达拉滨联合环磷酰胺、多柔比星、长春新碱和泼尼松方案免疫化疗延长疗程并序贯利妥昔单抗维持治疗未经治疗的老年套细胞淋巴瘤患者:芬兰淋巴瘤组的前瞻性研究。

Prolonged immunochemotherapy with rituximab, cytarabine and fludarabine added to cyclophosphamide, doxorubicin, vincristine and prednisolone and followed by rituximab maintenance in untreated elderly patients with mantle cell lymphoma: a prospective study by the Finnish Lymphoma Group.

机构信息

Department of Hematology, Helsinki University Central Hospital, Helsinki, Finland.

出版信息

Leuk Lymphoma. 2012 Oct;53(10):1920-8. doi: 10.3109/10428194.2012.672736. Epub 2012 Apr 23.

Abstract

There is no consensus on treatment strategies for elderly patients with mantle cell lymphoma (MCL). In this prospective phase II study we investigated whether the poor outcome could be improved, with reasonable toxicity, by prolonging the immunochemotherapy. Ten cycles of alternating cyclophosphamide, doxorubicin, vincristine and prednisolone (CHOP)/cytarabine (AraC) with eight doses of rituximab (R) were given as induction. The potential synergism of intermediate-dose AraC and fludarabine was tested in cycles 6-8. Induction was followed by bimonthly rituximab maintenance for 2 years. The median age of the 60 included patients was 74 years, and the Mantle Cell Lymphoma International Prognostic Index (MIPI) was intermediate or high risk in 98% of the patients. The overall response rate was 95% (complete response/complete response unconfirmed 87%). The response of 11 patients improved with cycles 6-8 (R-fludarabine-AraC). Progression-free survival was 70% and overall survival 72% at 4 years, respectively. Treatment related mortality was 2%. Severe infections were rare, with only one grade 4 infection. More dose reductions were needed during fludarabine-containing courses as compared to R-AraC. In 20 patients a transient grade 4 neutropenia without severe infections was recorded during maintenance. In conclusion, elderly patients with MCL can be treated relatively intensively with acceptable toxicity.

摘要

对于老年套细胞淋巴瘤(MCL)患者,目前尚无治疗策略的共识。在这项前瞻性的 II 期研究中,我们通过延长免疫化疗来提高疗效,同时控制毒性。10 个周期的环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)/阿糖胞苷(AraC)与 8 个剂量的利妥昔单抗(R)交替进行诱导治疗。在第 6-8 周期中测试了中等剂量 AraC 和氟达拉滨的协同作用。诱导治疗后,每 2 个月给予利妥昔单抗维持治疗 2 年。纳入的 60 例患者的中位年龄为 74 岁,98%的患者的套细胞淋巴瘤国际预后指数(MIPI)为中高危。总缓解率为 95%(完全缓解/不完全缓解 87%)。11 例患者在第 6-8 周期(R-氟达拉滨-AraC)后缓解。4 年时无进展生存率和总生存率分别为 70%和 72%。治疗相关死亡率为 2%。严重感染罕见,仅有 1 例 4 级感染。与 R-AraC 相比,含氟达拉滨的疗程需要更多的剂量减少。在 20 例患者中,在维持治疗期间记录到短暂的 4 级中性粒细胞减少,无严重感染。总之,老年 MCL 患者可以接受相对强化且毒性可接受的治疗。

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