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R-MACLO-IVAM 方案联合维持治疗可诱导未经治疗的套细胞淋巴瘤获得持久缓解 - 长期随访结果。

R-MACLO-IVAM regimen followed by maintenance therapy induces durable remissions in untreated mantle cell lymphoma - Long term follow up results.

机构信息

Department of Medicine, Division of Hematology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.

Department of Medicine, Division of Internal Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.

出版信息

Am J Hematol. 2021 Jun 1;96(6):680-689. doi: 10.1002/ajh.26163. Epub 2021 Apr 7.

Abstract

We present long-term combined results of two clinical trials implementing R-MACLO-IVAM induction followed by thalidomide or rituximab maintenance in 44 patients with untreated mantle cell lymphoma (MCL). The first 22 patients (UM-MCL1 ClinicalTrials.gov identifier NCT00450801) received maintenance with thalidomide (200 mg daily until relapse/intolerable toxicity) and a subsequent cohort of 22 patients (UM-MCL2 ClinicalTrials.gov identifier NCT00878254) received rituximab (375 mg/m IV weekly × 4, repeated every 6 months for 3 years). Considering all 44 patients, 41 (93.2%) achieved complete response (CR), two (4.5%) partial response (PR), and one (2.3%) was not evaluated for response. With a median follow up of 7.2 years (range < 1 month to 16 years), the 5-year progression-free survival (PFS) was 55.6% (95% CI: 38.9%-69.4%) and median PFS 7.9 years (95% CI: 3.7-11 years). The 5-year OS was 83.3% (95% CI: 68.1%-91.7%) and median OS was not reached. Patients with blastic variant (n = 6) had a 5-year PFS and OS of 20.8% and 60%, respectively. Myelosuppression was the most common adverse event during immunochemotherapy. Long-term treatment-related mortality was 6.8%. Note, R-MACLO-IVAM followed by maintenance therapy is an effective regimen to induce long-term remission in MCL without need for consolidation with ASCT.

摘要

我们报告了两项临床试验的长期联合结果,这两项临床试验对未经治疗的套细胞淋巴瘤(MCL)患者采用 R-MACLO-IVAM 诱导治疗,随后分别采用沙利度胺或利妥昔单抗维持治疗,共纳入 44 例患者。前 22 例患者(UM-MCL1,临床试验.gov 标识符 NCT00450801)接受沙利度胺(每天 200mg,直到复发/无法耐受毒性)维持治疗,随后的 22 例患者(UM-MCL2,临床试验.gov 标识符 NCT00878254)接受利妥昔单抗(375mg/m2,静脉注射,每周 1 次×4 次,随后每 6 个月重复 3 年)。考虑到所有 44 例患者,41 例(93.2%)达到完全缓解(CR),2 例(4.5%)部分缓解(PR),1 例(2.3%)未评估缓解情况。中位随访 7.2 年(范围为<1 个月至 16 年),5 年无进展生存率(PFS)为 55.6%(95%可信区间:38.9%-69.4%),中位 PFS 为 7.9 年(95%可信区间:3.7-11 年)。5 年总生存率(OS)为 83.3%(95%可信区间:68.1%-91.7%),中位 OS 未达到。存在母细胞样变异(n=6)的患者 5 年 PFS 和 OS 分别为 20.8%和 60%。免疫化疗期间最常见的不良反应是骨髓抑制。长期治疗相关死亡率为 6.8%。需要注意的是,R-MACLO-IVAM 诱导治疗后采用维持治疗是一种有效的方案,可诱导 MCL 长期缓解,无需进行 ASCT 巩固治疗。

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