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利妥昔单抗联合苯丁酸氮芥作为套细胞淋巴瘤一线治疗:一种高效方案。

Combination of rituximab with chlorambucil as first line treatment in patients with mantle cell lymphoma: a highly effective regimen.

机构信息

Department of Hematology, Athens Medical Center-Psychikon Branch, Laikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Leuk Lymphoma. 2011 Mar;52(3):387-93. doi: 10.3109/10428194.2010.534518. Epub 2010 Dec 6.

Abstract

The optimal treatment approach for patients with mantle cell lymphoma (MCL) is not well defined. Intensive therapeutic regimens result in high response rates and prolonged progression-free survival but at the expense of significant toxicity. We report here our results of the administration of rituximab plus chlorambucil (R-Chl) as first line treatment in patients with MCL. Twenty consecutively diagnosed patients were treated with this combination in which an induction and a maintenance arm were included. During induction, rituximab was administered at a dose of 375 mg/m(2) on day 1, while chlorambucil was given afterward at a dose of 10 mg/day for 10 consecutive days for eight cycles and then as a single agent for an additional four cycles. Maintenance consisted of rituximab administration every 2 months for 1 year. Most patients had indolent disease features such as a low mantle-cell international prognostic index (MIPI) score. The overall response rate was 95% (90% CR, 5% PR). Among patients in CR, 78% presented a molecular remission. The 3-year progression-free survival was 89%. There were no serious side effects. These results show that the R-Chl combination could be an effective therapeutic option as first line treatment in MCL, especially for patients with indolent disease characteristics.

摘要

套细胞淋巴瘤(MCL)患者的最佳治疗方法尚未明确。强化治疗方案可获得较高的缓解率和无进展生存期,但代价是显著的毒性。我们在此报告了我们采用利妥昔单抗联合苯丁酸氮芥(R-Chl)作为 MCL 患者一线治疗的结果。20 例连续诊断的患者接受了这种联合治疗,其中包括诱导期和维持期。在诱导期,利妥昔单抗的剂量为 375mg/m2,于第 1 天给药,而苯丁酸氮芥随后以 10mg/天的剂量给药,连续给药 10 天,共 8 个周期,然后作为单一药物再给药 4 个周期。维持治疗包括利妥昔单抗每 2 个月给药 1 年。大多数患者具有惰性疾病特征,如低套细胞国际预后指数(MIPI)评分。总体缓解率为 95%(完全缓解率 90%,部分缓解率 5%)。在完全缓解的患者中,78%的患者出现了分子缓解。3 年无进展生存率为 89%。没有严重的副作用。这些结果表明,R-Chl 联合方案可能是 MCL 一线治疗的有效治疗选择,特别是对于具有惰性疾病特征的患者。

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