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美国人类 T 细胞嗜淋巴细胞病毒 1 相关成人 T 细胞淋巴瘤白血病异体造血干细胞移植的障碍:来自主要三级中心大型队列的经验。

Barriers to Allogeneic Hematopoietic Stem Cell Transplantation for Human T Cell Lymphotropic Virus 1-Associated Adult T Cell Lymphoma-Leukemia in the United States: Experience from a Large Cohort in a Major Tertiary Center.

机构信息

Department of Medical Oncology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

Biol Blood Marrow Transplant. 2019 Jun;25(6):e199-e203. doi: 10.1016/j.bbmt.2019.02.004. Epub 2019 Feb 12.

Abstract

In the United States adult T cell lymphoma-leukemia (ATLL) carries a dismal prognosis and mainly affects immigrants from human T cell lymphotropic virus 1 endemic areas. Allogeneic hematopoietic stem cell transplant (alloHSCT) can be effective and is recommended as an upfront treatment in the National Comprehensive Cancer Network guidelines. We studied the barriers to alloHSCT in one of the largest ATLL populations in the United States. Comprehensive chart and donor registry reviews were conducted for 88 ATLL patients treated at Montefiore Medical Center from 2003 to 2018. Among 49 patients with acute and 32 with lymphomatous subtypes, 48 (59.5%) were ineligible for alloHSCT because of early mortality (52%), loss to follow-up (21%), uninsured status (15%), patient declination (10%), and frailty (2%). Among 28 HLA-typed eligible patients (34.6%), matched related donors were identified for 7 (25%). A matched unrelated donor (MUD) search yielded HLA-matched in 2 patients (9.5%), HLA mismatched in 6 (28.5%), and no options in 13 (62%). Haploidentical donors were identified for 6 patients (46%) with no unrelated options. There were no suitable donors for 7 (25%) alloHSCT-eligible patients. The main limitation for alloHSCT after donor identification was death from progressive disease (82%). AlloHSCT was performed in 10 patients (12.3%) and was associated with better relapse-free survival (26 versus 11 months, P = .04) and overall survival (47 versus 10 months, P = .03). Early mortality and progressive disease are the main barriers to alloHSCT, but poor follow-up, uninsured status, and lack of suitable donor, including haploidentical, are also substantial limitations that might disproportionally affect this vulnerable population. AlloHSCT can achieve long-term remissions, and strategies aiming to overcome these barriers are urgently needed to improve outcomes in ATLL.

摘要

在美国,成人 T 细胞淋巴瘤白血病(ATLL)预后较差,主要影响来自人类 T 细胞嗜淋巴细胞病毒 1 流行地区的移民。同种异体造血干细胞移植(alloHSCT)可能有效,并且被国家综合癌症网络指南推荐为一线治疗方法。我们研究了在美国最大的 ATLL 人群之一中 alloHSCT 的障碍。对 2003 年至 2018 年在 Montefiore 医疗中心治疗的 88 例 ATLL 患者进行了全面的图表和供者登记册审查。在 49 例急性和 32 例淋巴瘤型病例中,有 48 例(59.5%)因早期死亡率(52%)、失访(21%)、无保险状态(15%)、患者拒绝(10%)和虚弱(2%)而不适合 alloHSCT。在 28 例 HLA 分型合格的患者(34.6%)中,确定了 7 例(25%)有匹配的亲缘供者。在 2 例患者(9.5%)中找到了 HLA 匹配的无关供者,在 6 例患者(28.5%)中找到了 HLA 不匹配的无关供者,在 13 例患者(62%)中找不到供者。在没有无关供者选择的情况下,为 6 例患者(46%)确定了单倍体相合供者。对于 7 例(25%)alloHSCT 合格的患者没有合适的供者。在确定供者后进行 alloHSCT 的主要限制是疾病进展导致的死亡(82%)。10 例患者(12.3%)进行了 alloHSCT,无疾病复发存活率(26 个月与 11 个月,P=0.04)和总存活率(47 个月与 10 个月,P=0.03)均有改善。早期死亡率和疾病进展是 alloHSCT 的主要障碍,但不良随访、无保险状态以及缺乏合适的供者,包括单倍体相合供者,也是巨大的限制因素,可能会不成比例地影响这一弱势群体。alloHSCT 可实现长期缓解,迫切需要制定策略来克服这些障碍,以改善 ATLL 的结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415c/7558434/f30c8f439eef/nihms-1629472-f0001.jpg

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Adult T Cell Leukemia-Lymphoma (ATL): State of the Art.成人 T 细胞白血病-淋巴瘤(ATL):最新进展。
Curr Hematol Malig Rep. 2018 Aug;13(4):300-307. doi: 10.1007/s11899-018-0458-6.

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