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异基因造血干细胞移植后复发患者接受供者淋巴细胞输注和细胞因子诱导的杀伤细胞序贯输注的 II 期研究。

Phase II Study of Sequential Infusion of Donor Lymphocyte Infusion and Cytokine-Induced Killer Cells for Patients Relapsed after Allogeneic Hematopoietic Stem Cell Transplantation.

机构信息

USS Center of Cell Therapy "G. Lanzani" ASST Papa Giovanni XXIII Bergamo, Bergamo,Italy.

USC Hematology and Bone Marrow Transplant Unit ASST Papa Giovanni XXIII Bergamo, Bergamo, Italy.

出版信息

Biol Blood Marrow Transplant. 2017 Dec;23(12):2070-2078. doi: 10.1016/j.bbmt.2017.07.005. Epub 2017 Jul 13.

DOI:10.1016/j.bbmt.2017.07.005
PMID:28712935
Abstract

Seventy-four patients who relapsed after allogeneic stem cell transplantation were enrolled in a phase IIA study and treated with the sequential infusion of donor lymphocyte infusion (DLI) followed by cytokine-induced killer (CIK) cells. Seventy-three patients were available for the intention to treat analysis. At least 1 infusion of CIK cells was given to 59 patients, whereas 43 patients received the complete cell therapy planned (58%). Overall, 12 patients (16%) developed acute graft-versus-host disease (aGVHD) of grades I to II in 7 cases and grades III to IV in 5). In 8 of 12 cases, aGVHD developed during DLI treatment, leading to interruption of the cellular program in 3 patients, whereas in the remaining 5 cases aGVHD was controlled by steroids treatment, thus allowing the subsequent planned administration of CIK cells. Chronic GVHD (cGVHD) was observed in 11 patients (15%). A complete response was observed in 19 (26%), partial response in 3 (4%), stable disease in 8 (11%), early death in 2 (3%), and disease progression in 41 (56%). At 1 and 3 years, rates of progression-free survival were 31% and 29%, whereas rates of overall survival were 51% and 40%, respectively. By multivariate analysis, the type of relapse, the presence of cGVHD, and a short (<6 months) time from allogeneic hematopoietic stem cell transplantation to relapse were the significant predictors of survival. In conclusion, a low incidence of GVHD is observed after the sequential administration of DLI and CIK cells, and disease control can be achieved mostly after a cytogenetic or molecular relapse.

摘要

74 例异基因造血干细胞移植后复发的患者入组一项 2 期 A 研究,并接受序贯输注供者淋巴细胞输注(DLI)继之以细胞因子诱导的杀伤(CIK)细胞治疗。73 例患者可进行意向治疗分析。59 例患者至少输注 1 次 CIK 细胞,而 43 例患者接受了计划的完整细胞治疗(58%)。总体而言,12 例患者(16%)发生 1 至 2 级急性移植物抗宿主病(aGVHD)7 例,3 至 4 级 5 例。在 12 例中,8 例在 DLI 治疗期间发生 aGVHD,导致 3 例中断细胞治疗程序,而其余 5 例 aGVHD 通过皮质类固醇治疗得到控制,从而允许随后计划给予 CIK 细胞。11 例患者(15%)观察到慢性移植物抗宿主病(cGVHD)。19 例(26%)观察到完全缓解,3 例(4%)部分缓解,8 例(11%)疾病稳定,2 例(3%)早期死亡,41 例(56%)疾病进展。1 年和 3 年时,无进展生存率分别为 31%和 29%,总生存率分别为 51%和 40%。通过多变量分析,复发类型、cGVHD 的存在以及异基因造血干细胞移植后至复发的时间(<6 个月)是生存的显著预测因素。总之,DLI 和 CIK 细胞序贯给药后观察到 GVHD 发生率低,且在细胞遗传学或分子复发后可实现疾病控制。

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