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ECHELON-2 研究中一线应用 Brentuximab vedotin 联合 CHP 或 CHOP 方案后 CD30+PTCL 采用干细胞移植的作用。

Role of stem cell transplant in CD30+ PTCL following frontline brentuximab vedotin plus CHP or CHOP in ECHELON-2.

机构信息

Centre for Lymphoid Cancer and Division of Medical Oncology, British Columbia Cancer, Vancouver, BC, Canada.

Memorial Sloan-Kettering Cancer Center, New York, NY.

出版信息

Blood Adv. 2022 Oct 11;6(19):5550-5555. doi: 10.1182/bloodadvances.2020003971.

DOI:
10.1182/bloodadvances.2020003971
PMID:35470385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9647727/
Abstract

Peripheral T-cell lymphomas (PTCLs) are a heterogeneous group of aggressive non-Hodgkin lymphomas, the majority of which have high relapse rates following standard therapy. Despite use of consolidative stem cell transplant (SCT) following frontline therapy, there remains no consensus on its utility. The double-blind randomized phase 3 ECHELON-2 study (#NCT01777152; clinicaltrials.gov) demonstrated improved progression-free survival (PFS) and overall survival with frontline brentuximab vedotin plus cyclophosphamide, doxorubicin, and prednisone (A+CHP). Herein, we conducted an exploratory subgroups analysis of the impact of consolidative SCT on PFS in patients with previously untreated CD30+ PTCL (ALK- anaplastic large cell lymphoma [ALCL] and non-ALCL) who were in complete response (CR) after frontline treatment with A+CHP or cyclophosphamide, doxorubicin, vincristine, and prednisone. Median PFS follow-up was 47.57 months. The PFS hazard ratio was 0.36, equating to a 64% reduction in the risk of a PFS event in patients who underwent SCT. The median PFS in patients who underwent SCT was not reached, vs 55.66 months in patients who did not undergo SCT. PFS results favored the use of SCT in both ALK- ALCL and non-ALCL subgroups. These data support the consideration of consolidative SCT in patients with CD30+PTCL who achieve CR following treatment with A+CHP.

摘要

外周 T 细胞淋巴瘤 (PTCLs) 是一组异质性侵袭性非霍奇金淋巴瘤,大多数患者在标准治疗后复发率较高。尽管在前线治疗后使用巩固性干细胞移植 (SCT),但其应用仍存在争议。双盲随机 3 期 ECHELON-2 研究 (#NCT01777152; clinicaltrials.gov) 表明,在前线使用 Brentuximab vedotin 联合环磷酰胺、多柔比星和泼尼松 (A+CHP) 治疗后,无进展生存期 (PFS) 和总生存期得到改善。在此,我们对以前未经治疗的 CD30+PTCL(ALK-间变性大细胞淋巴瘤 [ALCL] 和非 ALCL)患者进行了一项探索性亚组分析,这些患者在一线 A+CHP 或环磷酰胺、多柔比星、长春新碱和泼尼松治疗后达到完全缓解 (CR),评估巩固性 SCT 对 PFS 的影响。中位 PFS 随访时间为 47.57 个月。PFS 风险比为 0.36,相当于接受 SCT 患者的 PFS 事件风险降低了 64%。接受 SCT 患者的中位 PFS 尚未达到,而未接受 SCT 患者的中位 PFS 为 55.66 个月。在 ALK- ALCL 和非 ALCL 亚组中,PFS 结果均有利于 SCT 的应用。这些数据支持在接受 A+CHP 治疗后达到 CR 的 CD30+PTCL 患者中考虑使用巩固性 SCT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e04d/9647727/542342671f29/BLOODA_ADV-2020-003971-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e04d/9647727/b47ff7e6204d/BLOODA_ADV-2020-003971-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e04d/9647727/542342671f29/BLOODA_ADV-2020-003971-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e04d/9647727/b47ff7e6204d/BLOODA_ADV-2020-003971-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e04d/9647727/542342671f29/BLOODA_ADV-2020-003971-gr2.jpg

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