Patriarca Francesca, Sperotto Alessandra, Lorentino Francesca, Oldani Elena, Mammoliti Sonia, Isola Miriam, Picardi Alessandra, Arcese William, Saporiti Giorgia, Sorasio Roberto, Mordini Nicola, Cavattoni Irene, Musso Maurizio, Borghero Carlo, Micò Caterina, Fanin Renato, Bruno Benedetto, Ciceri Fabio, Bonifazi Francesca
Clinica Ematologica e Centro Trapianti, Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.
Department of Medical Area (DAME) Università di Udine, Udine, Italy.
Front Oncol. 2020 Oct 15;10:572918. doi: 10.3389/fonc.2020.572918. eCollection 2020.
We conducted a retrospective multicenter study including pediatric and adult patients with acute leukemia (AL) who received donor lymphocyte infusions (DLIs) after allogeneic hematopoietic stem cell transplantation (HCT) between January 1, 2010 and December 31, 2015, in order to determine the efficacy and toxicity of the immune treatment. Two hundred fifty-two patients, median age 45.1 years (1.6-73.4), were enrolled from 34 Italian transplant centers. The underlying disease was acute myeloid leukemia in 180 cases (71%). Donors were HLA identical or 1 locus mismatched sibling (40%), unrelated (40%), or haploidentical (20%). The first DLI was administered at a median time of 258 days (55-3,784) after HCT. The main indication for DLI was leukemia relapse (73%), followed by mixed chimerism (17%), and pre-emptive/prophylactic use (10%). Ninety-six patients (38%) received one single infusion, whereas 65 (26%), 42 (17%), and 49 patients (19%) received 2, 3, or ≥4 infusions, respectively, with a median of 31 days between two subsequent DLIs. Forty percent of evaluable patients received no treatment before the first DLI, whereas radiotherapy, conventional chemotherapy or targeted treatments were administered in 3, 39, and 18%, respectively. In informative patients, a few severe adverse events were reported: grade III-IV graft versus host disease (GVHD) (3%), grade III-IV hematological toxicity (11%), and DLI-related mortality (9%). Forty-six patients (18%) received a second HCT after a median of 232 days (32-1,390) from the first DLI. With a median follow-up of 461 days (2-3,255) after the first DLI, 1-, 3-, and 5- year overall survival (OS) of the whole group from start of DLI treatment was 55, 39, and 33%, respectively. In multivariate analysis, older recipient age, and transplants from haploidentical donors significantly reduced OS, whereas DLI for mixed chimerism or as pre-emptive/prophylactic treatment compared to DLI for AL relapse and a schedule including more than one DLI significantly prolonged OS. This GITMO survey confirms that DLI administration in absence of overt hematological relapse and multiple infusions are associated with a favorable outcome in AL patients. DLI from haploidentical donors had a poor outcome and may represent an area of further investigation.
我们进行了一项回顾性多中心研究,纳入了2010年1月1日至2015年12月31日期间接受异基因造血干细胞移植(HCT)后接受供体淋巴细胞输注(DLI)的急性白血病(AL)儿科和成年患者,以确定免疫治疗的疗效和毒性。从34个意大利移植中心招募了252例患者,中位年龄45.1岁(1.6 - 73.4岁)。基础疾病为急性髓系白血病180例(71%)。供体为HLA全相合或1个位点不相合的同胞(40%)、无关供体(40%)或单倍体相合供体(20%)。首次DLI在HCT后中位时间258天(55 - 3784天)给予。DLI的主要适应证为白血病复发(73%),其次为混合嵌合体(17%)和抢先/预防性使用(10%)。96例患者(38%)接受单次输注,而65例(26%)、42例(17%)和49例患者(19%)分别接受2次、3次或≥4次输注,两次连续DLI之间的中位间隔时间为31天。40%的可评估患者在首次DLI前未接受治疗,而分别有3%、39%和18%的患者接受了放疗、传统化疗或靶向治疗。在有信息的患者中,报告了一些严重不良事件:III - IV级移植物抗宿主病(GVHD)(3%)、III - IV级血液学毒性(11%)和DLI相关死亡率(9%)。46例患者(18%)在首次DLI后中位时间232天(32 - 1390天)接受了第二次HCT。首次DLI后中位随访461天(2 - 3255天),从DLI治疗开始,全组1年、3年和5年总生存率(OS)分别为55%、39%和33%。多因素分析显示,受者年龄较大以及来自单倍体相合供体的移植显著降低OS,而与用于AL复发的DLI相比,用于混合嵌合体或抢先/预防性治疗的DLI以及包括不止一次DLI的方案显著延长OS。这项GITMO调查证实,在无明显血液学复发情况下给予DLI以及多次输注与AL患者的良好结局相关。来自单倍体相合供体的DLI结局较差,可能是一个需要进一步研究的领域。