首页> 外文期刊>Leukemia and lymphoma >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
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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

机译:利妥昔单抗,阿糖胞苷和氟达拉滨联合环磷酰胺,阿霉素,长春新碱和泼尼松龙的长期免疫化学疗法,然后对未治疗的老年套细胞淋巴瘤患者进行利妥昔单抗维持治疗:芬兰淋巴瘤小组的一项前瞻性研究

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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 68. 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 68 (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.
机译:对于老年套细胞淋巴瘤(MCL)患者的治疗策略尚无共识。在这项前瞻性II期研究中,我们研究了延长免疫化学疗法是否可以改善不良结局并具有合理的毒性。给予十个周期的交替的环磷酰胺,阿霉素,长春新碱和泼尼松龙(CHOP)/阿糖胞苷(AraC)和八剂利妥昔单抗(R)诱导。在第68个周期中测试了中等剂量AraC和氟达拉滨的潜在协同作用。诱导后,利妥昔单抗每两个月维持2年。纳入研究的60名患者的中位年龄为74岁,并且98%的患者的Mantle细胞淋巴瘤国际预后指数(MIPI)为中度或高风险。总体缓解率为95%(完全缓解/完全缓解未经确认为87%)。 11例患者的反应在68周期(R-氟达拉滨-AraC)时有所改善。 4年无进展生存率分别为70%和总生存率72%。与治疗相关的死亡率为2%。严重感染很少见,只有一种4级感染。与R-AraC相比,在含氟达拉滨的疗程中需要更多的剂量减少。在维持期间,记录了20例患者暂时没有严重感染的4级中性粒细胞减少症。总之,老年MCL患者可以接受相对较重的治疗,并具有可接受的毒性。

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