干细胞移植治疗htlv -1相关北美成人t细胞白血病/淋巴瘤的疗效

Abdul-Hamid Bazarbachi, Daniel Reef, Hiba Narvel, Riya Patel, Rama Al Hamed, Sindhu Vikash, Karun Neupane, Eleftheria Atalla, Astha Thakkar, Shafia Rahman, Urvi Shah, Diego Adrianzen-Herrera, Ryann Quinn, Sumaira Zareef, Emma Rabinovich, Alyssa De Castro, Felisha Joseph, Kailyn Gillick, Jennat Mustafa, Fariha Khatun, Amanda Lombardo, Latoya Townsend-Nugent, Michelly Abreu, Nicole Chambers, Richard Elkind, Yang Shi, Yanhua Wang, Olga Derman, Kira Gritsman, Ulrich Steidl, Mendel Goldfinger, Noah Kornblum, Aditi Shastri, Ioannis Mantzaris, Liza Bachier-Rodriguez, Nishi Shah, Dennis Cooper, Amit Verma, Bihui Hilda Ye, Murali Janakiram, Roberto Alejandro Sica
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引用次数: 1

摘要

成人t细胞白血病/淋巴瘤(ATLL)仍然具有挑战性的治疗和令人沮丧的结果。同种异体干细胞移植(Allogeneic stem cell transplantation, allo-SCT)有很好的结果,但数据仍然很少。在这项来自北美的100例ATLL患者(67例急性,22例淋巴瘤)的单中心回顾性分析中,17例接受了同种异体细胞移植,5例接受了自体细胞移植(ASCT),中位随访时间为65个月。移植后3年复发率(RI)和非复发死亡率(NRM)分别为51%和37%,3年无进展生存率(PFS)和总生存率(OS)分别为31%和35%。ASCT 1年的RI为80%,而同种异体sct为30% (p = 0.03)。校正不朽时间偏差后,allo-SCT显著改善了OS (HR = 0.4, p = 0.01)。在探索性多变量分析中,获得首次完全缓解且Karnofsky评分≥90的患者具有明显更好的结果,与西班牙裔患者相比,黑人患者的结果更差。在移植患者中,14例在2年内死亡,其中4例为ASCT受者。我们的数据是迄今为止日本和欧洲以外最大的ATLL移植队列。我们表明,同种异体细胞移植,而不是ASCT,是一种有效的选择,在选择的ATLL患者中,可以诱导长期生存,40%的患者在5年后存活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Outcome of Stem Cell Transplantation in HTLV-1-Associated North American Adult T-Cell Leukemia/Lymphoma.

Outcome of Stem Cell Transplantation in HTLV-1-Associated North American Adult T-Cell Leukemia/Lymphoma.

Outcome of Stem Cell Transplantation in HTLV-1-Associated North American Adult T-Cell Leukemia/Lymphoma.

Outcome of Stem Cell Transplantation in HTLV-1-Associated North American Adult T-Cell Leukemia/Lymphoma.

Adult T-cell leukemia/lymphoma (ATLL) remains challenging to treat and has dismal outcome. Allogeneic stem-cell transplantation (allo-SCT) has promising results, but data remain scarce. In this single-center retrospective analysis of 100 patients with ATLL from north America (67 acute, 22 lymphomatous), 17 underwent allo-SCT and 5 autologous SCT (ASCT), with a median follow-up of 65 months. Post-transplant 3-years relapse incidence (RI) and non-relapse mortality (NRM) were 51% and 37%, respectively, and 3-year progression-free survival (PFS) and overall survival (OS) were 31% and 35%, respectively. ASCT 1-year RI was 80% compared to 30% in allo-SCT (p = 0.03). After adjusting for immortal-time bias, allo-SCT had significantly improved OS (HR = 0.4, p = 0.01). In exploratory multivariate analysis, patients achieving first complete response and Karnofsky score ≥ 90 had significantly better outcomes, as did Black patients, compared to Hispanics, who had worse outcome. In transplanted patients, 14 died within 2 years, 4 of which ASCT recipients. Our data are the largest ATLL transplant cohort presented to date outside of Japan and Europe. We show that allo-SCT, but not ASCT, is a valid option in select ATLL patients, and can induce long term survival, with 40% of patients alive after more than 5 years.

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