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来那度胺联合 R-CHOP 方案治疗滤泡性淋巴瘤转化的弥漫性大 B 细胞淋巴瘤新诊患者的疗效:来自 2 期 MC078E 研究的结果。

Lenalidomide in combination with R-CHOP produces high response rates and progression-free survival in new, untreated diffuse large B-cell lymphoma transformed from follicular lymphoma: results from the Phase 2 MC078E study.

机构信息

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.

出版信息

Blood Cancer J. 2021 Sep 25;11(9):160. doi: 10.1038/s41408-021-00542-z.

Abstract

Diffuse large B-cell lymphoma (DLBCL), either concurrent with or transformed from follicular lymphoma (FL) is often excluded from clinical trials. Lenalidomide has response rates of 45% in relapsed transformed DLBCL. Herein we present an analysis of MC078E, a phase II clinical trial testing lenalidomide plus R-CHOP (R2CHOP) for patients with untreated transformed/concurrent DLBCL (NCT00670358). Adult patients with transformed or concurrent DLBCL were included. Patients received six cycles of rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (R-CHOP) with lenalidomide 25 mg days 1-10 of each cycle. The primary outcome was progression-free survival (PFS) at 24 months. Secondary outcomes were response rates, event-free survival (EFS), and overall survival (OS). Thirty-nine patients were accrued from August 5, 2013 to July 28, 2020 and 33 were eligible by central pathology review. The median age was 64 (24-80) years, 18 (54%) were male, 25 (76%) were concurrent and 8 (24%) were transformed DLBCL. The PFS, EFS, and OS rates at 24 months were 84.4% (CI: 67.2-94.7%), 84.5% (CI: 72.9-98%), and 97.0% (CI: 91.3-100%), respectively. R2CHOP is effective in concurrent and transformed DLBCL. The study supports the inclusion of anthracycline-naive transformed and concurrent DLBCL in future clinical trials of novel immunomodulatory analogues.

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL),无论是并发还是由滤泡性淋巴瘤(FL)转化而来,通常都被排除在临床试验之外。来那度胺在复发转化的 DLBCL 中的缓解率为 45%。在此,我们报告了 MC078E 的分析结果,这是一项测试来那度胺联合 R-CHOP(R2CHOP)治疗未经治疗的转化/并发 DLBCL 患者的 II 期临床试验(NCT00670358)。纳入了转化或并发 DLBCL 的成年患者。患者接受六个周期的利妥昔单抗、环磷酰胺、多柔比星、长春新碱、泼尼松(R-CHOP),每个周期的第 1-10 天给予来那度胺 25mg。主要终点是 24 个月时的无进展生存期(PFS)。次要终点是缓解率、无事件生存期(EFS)和总生存期(OS)。39 例患者于 2013 年 8 月 5 日至 2020 年 7 月 28 日入组,33 例经中心病理复查合格。中位年龄为 64(24-80)岁,18 例(54%)为男性,25 例(76%)为并发 DLBCL,8 例(24%)为转化性 DLBCL。24 个月时的 PFS、EFS 和 OS 率分别为 84.4%(CI:67.2-94.7%)、84.5%(CI:72.9-98%)和 97.0%(CI:91.3-100%)。R2CHOP 对并发和转化性 DLBCL 有效。该研究支持在新型免疫调节类似物的未来临床试验中纳入蒽环类药物初治的转化和并发 DLBCL。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08c/8464592/943e1d18a676/41408_2021_542_Fig1_HTML.jpg

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