自体干细胞移植治疗NK/ t细胞淋巴瘤:EBMT淋巴瘤工作组开展的一项多国队列a研究中EBV-DNA对预后的影响

IF 14.6 2区 医学 Q1 HEMATOLOGY
HemaSphere Pub Date : 2025-08-15 DOI:10.1002/hem3.70184
Philipp Berning, Maud Ngoya, Won Seog Kim, Evgenii Shumilov, Depei Wu, Haiwen Huang, Anne Cairoli, Alessandra Tucci, Guillaume Dachy, Romain Gounot, Anne C. Wilke, Christof Scheid, Peter Dreger, Jose Luis Lopez Lorenzo, Adrian Bloor, Joanna Romejko-Jarosinska, Alain Gadisseur, Roland Schroers, Péter Reményi, Ludovic Gabellier, Monica Poiani, Khalid Halahleh, Jacques-Emmanuel Galimard, Georg Lenz, Anna Sureda, Ali Bazarbachi, Bertram Glass, Norbert Schmitz
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引用次数: 0

摘要

自然杀伤(NK)/ t细胞淋巴瘤(NKTCLs)是一种罕见的侵袭性淋巴瘤,常见于东亚和南美。尽管在很大程度上由于基于天冬酰胺酶的治疗而有所改善,但晚期疾病的预后仍然很差,自体干细胞移植(auto-HCT)的作用仍然存在争议。本研究评估了亚洲和欧洲NKTCL患者auto-HCT的实际结果。我们纳入了2011年至2022年间接受auto-HCT的130名成人NKTCL患者,使用的数据来自欧洲血液和骨髓移植协会(EBMT)登记和韩国登记数据。中位年龄51.3岁;66.9%为男性。大多数患者(95.1%)的东部肿瘤合作组(ECOG)评分为0-1;65.3%为III-IV期。53.1%的患者有一条既往治疗线,46.9%的患者有≥2条既往治疗线。移植前使用以天冬酰胺酶为基础的方案者占79.5%。auto-HCT的应答包括完全缓解(59.7%)、部分缓解(27.9%)和疾病稳定/进展(12.4%)。外周血eb病毒dna阳性率为37.3%。中位随访4.6年,3年总生存期(OS)和无进展生存期(PFS)分别为63.8%和47.6%。3年复发率46.7%,NRM 5.7%。与PR(52.8%)和疾病稳定/进展(32.0%)相比,完全缓解患者的3年OS(75.2%)得到改善(P = 0.007)。在auto-HCT检测中,血液中可检测到EBV-DNA的患者预后较差(3年OS: 26.7% vs. 78.1%;P < 0.0001)。在auto-HCT前获得完全缓解且血液中检测不到EBV-DNA的患者生存率较高,这表明auto-HCT可能是选定高危患者的一种治疗选择。这是评估NKTCL auto-HCT预后因素的最大的跨国队列研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Autologous stem cell transplantation in NK/T-cell lymphoma: Prognostic impact of EBV-DNA in a multinational cohort—A study by the EBMT Lymphoma Working Party

Autologous stem cell transplantation in NK/T-cell lymphoma: Prognostic impact of EBV-DNA in a multinational cohort—A study by the EBMT Lymphoma Working Party

Natural killer (NK)/T-cell lymphomas (NKTCLs) are rare, aggressive lymphomas prevalent in East Asia and South America. Despite improvements, largely due to asparaginase-based therapies, outcomes for advanced disease remain poor, and the role of autologous stem cell transplantation (auto-HCT) remains controversial. This study evaluated real-world outcomes of auto-HCT in NKTCL patients across Asia and Europe. We included 130 adult NKTCL patients undergoing auto-HCT between 2011 and 2022 using data from the European Society for Blood and Marrow Transplantation (EBMT) registry and South Korean registry data. Median age was 51.3 years; 66.9% were male. Most patients (95.1%) had an Eastern Cooperative Oncology Group (ECOG) score 0–1; 65.3% had Stage III–IV disease. One prior therapy line was reported in 53.1%, and ≥2 lines in 46.9%. Asparaginase-based regimens were used in 79.5% pretransplant. Responses at auto-HCT included complete (59.7%), partial (27.9%) remission, and stable/progressive disease (12.4%). Epstein–Barr virus (EBV)-DNA in the peripheral blood was reported in 37.3%. With a median follow-up of 4.6 years, 3-year overall survival (OS) and progression-free survival (PFS) were 63.8% and 47.6%. Relapse and NRM rates at 3 years were 46.7% and 5.7%. Patients in complete remission had improved 3-year OS (75.2%) compared to PR (52.8%) and stable/progressive disease (32.0%) (P = 0.007). Detectable EBV-DNA in the blood at auto-HCT was associated with poor outcomes (3-year OS: 26.7% vs. 78.1% in patients with undetectable EBV-DNA; P < 0.0001). Patients achieving complete remission and undetectable EBV-DNA in the blood before auto-HCT had a favorable survival, suggesting auto-HCT may be a treatment option in selected high-risk patients. This is the largest multinational cohort evaluating prognostic factors for auto-HCT for NKTCL.

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来源期刊
HemaSphere
HemaSphere Medicine-Hematology
CiteScore
6.10
自引率
4.50%
发文量
2776
审稿时长
7 weeks
期刊介绍: HemaSphere, as a publication, is dedicated to disseminating the outcomes of profoundly pertinent basic, translational, and clinical research endeavors within the field of hematology. The journal actively seeks robust studies that unveil novel discoveries with significant ramifications for hematology. In addition to original research, HemaSphere features review articles and guideline articles that furnish lucid synopses and discussions of emerging developments, along with recommendations for patient care. Positioned as the foremost resource in hematology, HemaSphere augments its offerings with specialized sections like HemaTopics and HemaPolicy. These segments engender insightful dialogues covering a spectrum of hematology-related topics, including digestible summaries of pivotal articles, updates on new therapies, deliberations on European policy matters, and other noteworthy news items within the field. Steering the course of HemaSphere are Editor in Chief Jan Cools and Deputy Editor in Chief Claire Harrison, alongside the guidance of an esteemed Editorial Board comprising international luminaries in both research and clinical realms, each representing diverse areas of hematologic expertise.
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