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在T细胞去除的匹配相关供体异基因造血细胞移植后进行剂量递增预防性供体淋巴细胞输注是可行的,并且会导致更高的供体嵌合率、更快的免疫重建以及无进展生存期延长。

Dose escalation prophylactic donor lymphocyte infusion after T-cell depleted matched related donor allogeneic hematopoietic cell transplantation is feasible and results in higher donor chimerism, faster immune re-constitution, and prolonged progression-free survival.

作者信息

Kothari Shawn, Artz Andrew S, Lee Sang Mee, Fulton Noreen, Park Jae-Hyun, Stock Wendy, Larson Richard A, Odenike Olatoyosi, Kline Justin, LaBelle James, Kosuri Satyajit, Riedell Peter, Nakamura Yusuke, Bishop Michael R, Liu Hongtao

机构信息

Section of Hematology/Oncology, Department of Medicine and Comprehensive Cancer Center, University of Chicago, Chicago, IL, USA.

Department of Public Health Sciences, The University of Chicago, Chicago, IL, USA.

出版信息

Bone Marrow Transplant. 2020 Jun;55(6):1161-1168. doi: 10.1038/s41409-020-0798-4. Epub 2020 Jan 28.

Abstract

Prophylactic donor lymphocyte infusion (pDLI) is a potential intervention to prolong remission for patients receiving allogeneic hematopoietic stem cell transplantation (allo-SCT), however, the optimal timing and dose are unknown. We conducted a prospective trial exploring the feasibility of early withdrawal of immunosuppression (WOI) at day 60 followed by dose escalation of pDLI after alemtuzumab-based, T-cell depleted conditioning for patients with high-risk hematologic malignancies. pDLI were administered at day 75 to day 90 and again in 4-8 week intervals with receipt of up to 5 pDLI infusions. Fourty-six patients with matched-related donors (MRD) and 29 patients with matched-unrelated donors (MUD) were considered. Twenty-eight MRD patients were able to undergo WOI, 26 patients (93%) received at least 1 DLI, 16 patients (57%) received 3+, and 7 patients (25%) received 5 pDLI. Only 7 MUD patients were able to undergo WOI, 4 (57%) received at least 1 pDLI, 1 patient (14%) received 3 DLI, and no patients received all 5. Median PFS for patients on the study was 366 days. The estimated 2-year PFS and OS rates for all patients were 41% (95% CI, 32-54%) and 51% (95% CI, 41-63%) compared with 57% (95% CI, 41-77%) and 67% (95% CI, 52-86%) for patients who received at least one pDLI. In addition, MRD patients receiving pDLI had faster immune re-constitution and improved donor chimerism. Our trial proposes a novel dosage and treatment schedule for pDLI that is tolerable for patients who have received MRD allo-SCT and leads to improved outcomes.

摘要

预防性供体淋巴细胞输注(pDLI)是一种可能延长接受异基因造血干细胞移植(allo-SCT)患者缓解期的干预措施,然而,最佳时机和剂量尚不清楚。我们进行了一项前瞻性试验,探讨在第60天早期停用免疫抑制(WOI)的可行性,随后对高危血液系统恶性肿瘤患者在基于阿仑单抗的T细胞清除预处理后进行pDLI剂量递增。pDLI在第75天至第90天给药,并以4至8周的间隔再次给药,最多接受5次pDLI输注。研究了46例有匹配相关供体(MRD)的患者和29例有匹配无关供体(MUD)的患者。28例MRD患者能够进行WOI,26例患者(93%)接受了至少1次DLI,16例患者(57%)接受了3次及以上,7例患者(25%)接受了5次pDLI。只有7例MUD患者能够进行WOI,4例(57%)接受了至少1次pDLI,1例患者(14%)接受了3次DLI,没有患者接受全部5次。研究中患者的中位无进展生存期(PFS)为366天。所有患者的估计2年PFS和总生存期(OS)率分别为41%(95%CI,32-54%)和51%(95%CI,41-63%),而接受至少1次pDLI的患者分别为57%(95%CI,41-77%)和67%(95%CI,52-86%)。此外,接受pDLI的MRD患者免疫重建更快,供体嵌合率提高。我们的试验提出了一种新的pDLI剂量和治疗方案,该方案对于接受MRD allo-SCT的患者是可耐受的,并能改善预后。

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