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