Autologous stem cell transplantation in T-cell/histiocyte-rich large B-cell lymphoma: EBMT Lymphoma Working Party study.

IF 7.4 1区 医学 Q1 HEMATOLOGY
Simon Renders, Maud Ngoya, Herve Finel, Marie-Thérèse Rubio, William M Townsend, Roland Schroers, Urban Novak, Nicolaas Schaap, Mahmoud Aljurf, Grzegorz Helbig, Matthew Collin, Guido Kobbe, Huynh Anne, José Antonio Antonio Pérez-Simón, Adrian Bloor, Hervé Ghesquieres, Anna Sureda, Norbert Schmitz, Bertram Glass, Peter Dreger
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Abstract

Although broadly employed, consolidative autologous hematopoietic stem cell transplantation (autoHCT) for relapsed/refractory (r/r) T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL) has never been specifically investigated. Here we have analyzed outcomes of autoHCT for THRLBCL compared to diffuse large cell B-cell lymphoma not otherwise specified (DLBCL). Eligible for this retrospective registry study were adult patients with r/r THRLBCL and DLBCL, respectively, who underwent a first autoHCT in a salvage-sensitive disease status as assessed by PET-CT between 2016 and 2021 and were registered with the European Society for Blood and Marrow Transplantation (EBMT) database. Primary endpoint was progression-free survival (PFS) 2 years after transplantation. Two-hundred-one patients with THRLBCL and 5,543 with DLBCL were included. There were no significant differences in terms of disease status at HCT, pretreatment lines, and interval from diagnosis to transplant between the cohorts, but patients with THRBCL were significantly younger, contained a higher proportion of men, and had a better performance status. Compared to DLBCL, THRLBCL was associated with significantly better 2-year PFS (78% vs. 59%; p<0.001) and overall survival (OS; 81% vs. 74%; p=0.02) because of a significantly lower 2-year relapse incidence (RI; 16% vs. 35%; p<0.001). On multivariate analysis, favorable relapse risk (hazard ratio (HR) 0.46, 95%CI 0.31-0.7) and PFS (HR 0.58, 95%CI 0.41-0.82) of patients with THRLBCL remained significant, while OS benefits (HR 0.78, 95%CI 0.54-1.12) did not. These results were validated in a propensity-score matched analysis. These data prove autoHCT as an effective treatment option for salvage-sensitive r/r THRLBCL.

T细胞/组织细胞丰富的大B细胞淋巴瘤的自体干细胞移植:EBMT淋巴瘤工作组研究。
虽然自体造血干细胞移植(autoHCT)已被广泛应用于治疗复发/难治性(r/r)T细胞/组织细胞丰富的大B细胞淋巴瘤(THRLBCL),但从未进行过专门的研究。在此,我们分析了自体血细胞移植治疗THRLBCL与非特异性弥漫大细胞B细胞淋巴瘤(DLBCL)的疗效比较。有资格参与这项回顾性登记研究的患者分别是r/r THRLBCL和DLBCL成人患者,他们在2016年至2021年期间接受了首次自体HCT,经PET-CT评估处于挽救敏感疾病状态,并在欧洲血液和骨髓移植学会(EBMT)数据库中进行了登记。主要终点是移植后两年的无进展生存期(PFS)。共纳入了211名THRLBCL患者和5543名DLBCL患者。两组患者在接受造血干细胞移植时的疾病状态、预处理线以及从诊断到移植的间隔时间方面没有明显差异,但THRBCL患者明显更年轻,男性比例更高,表现状态更好。与DLBCL相比,THRLBCL的2年PFS明显更好(78% vs. 59%; p
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来源期刊
Blood advances
Blood advances Medicine-Hematology
CiteScore
12.70
自引率
2.70%
发文量
840
期刊介绍: Blood Advances, a semimonthly medical journal published by the American Society of Hematology, marks the first addition to the Blood family in 70 years. This peer-reviewed, online-only, open-access journal was launched under the leadership of founding editor-in-chief Robert Negrin, MD, from Stanford University Medical Center in Stanford, CA, with its inaugural issue released on November 29, 2016. Blood Advances serves as an international platform for original articles detailing basic laboratory, translational, and clinical investigations in hematology. The journal comprehensively covers all aspects of hematology, including disorders of leukocytes (both benign and malignant), erythrocytes, platelets, hemostatic mechanisms, vascular biology, immunology, and hematologic oncology. Each article undergoes a rigorous peer-review process, with selection based on the originality of the findings, the high quality of the work presented, and the clarity of the presentation.
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