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苯达莫司汀、环磷酰胺和利妥昔单抗治疗惰性非霍奇金淋巴瘤的长期总生存和无进展生存。

Long-term overall- and progression-free survival after pentostatin, cyclophosphamide and rituximab therapy for indolent non-Hodgkin lymphoma.

机构信息

Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Internal Medicine, Lankenau Medical Center, Wynnewood, PA, USA.

出版信息

Br J Haematol. 2019 May;185(4):670-678. doi: 10.1111/bjh.15814. Epub 2019 Feb 28.

DOI:10.1111/bjh.15814
PMID:30820940
Abstract

In a prospective phase II trial, pentostatin combined with cyclophosphamide and rituximab (PCR) induced strong responses and was well-tolerated in previously untreated patients with advanced-stage, indolent non-Hodgkin lymphoma (iNHL). After a median patient follow-up of more than 108 months, we performed an intent-to-treat analysis of our 83 participants. Progression-free survival (PFS) rates at 108 months for follicular lymphoma (FL), marginal zone lymphoma (MZL) and small lymphocytic lymphoma (SLL) were 71%, 67% and 15%, respectively, and were affected by clinicopathological characteristics. Ten-year PFS rates for those with beta-2-microglobulin levels <2·2 and ≥2·2 mg/l prior to treatment were 71% and 21%, respectively. Patients without bone marrow involvement had 10-year PFS rates of 72% vs. 29% for those with involvement. At time of analysis, the median overall survival (OS) had not been reached. The OS rate was 64% at 10 years and differed significantly based on histology: 94% for FL, 66% for MZL and 39% for SLL. Long-term toxicities included 18 (21·7%) patients with second malignancies and 2 (2·4%) who developed myelodysplastic syndrome after receiving additional lines of chemotherapy. Our 10-year follow-up analysis confirms that PCR is an effective, robust and tolerable treatment regimen for patients with iNHL.

摘要

在一项前瞻性的 II 期临床试验中,喷司他丁联合环磷酰胺和利妥昔单抗(PCR)在未经治疗的晚期惰性非霍奇金淋巴瘤(iNHL)患者中诱导了强烈的反应,并具有良好的耐受性。在中位患者随访超过 108 个月后,我们对 83 名参与者进行了意向治疗分析。108 个月时滤泡性淋巴瘤(FL)、边缘区淋巴瘤(MZL)和小淋巴细胞淋巴瘤(SLL)的无进展生存(PFS)率分别为 71%、67%和 15%,并受临床病理特征的影响。治疗前β-2-微球蛋白水平<2.2 和≥2.2mg/l 的患者,10 年 PFS 率分别为 71%和 21%。无骨髓受累的患者 10 年 PFS 率为 72%,而受累患者为 29%。在分析时,中位总生存(OS)尚未达到。10 年 OS 率为 64%,且根据组织学显著不同:FL 为 94%,MZL 为 66%,SLL 为 39%。长期毒性包括 18 名(21.7%)患者发生第二恶性肿瘤和 2 名(2.4%)患者在接受额外化疗后发生骨髓增生异常综合征。我们的 10 年随访分析证实,PCR 是 iNHL 患者有效、强大且耐受良好的治疗方案。

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