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CD45RA+ 耗尽供者淋巴细胞输注在异基因造血干细胞移植后环磷酰胺治疗血液系统恶性肿瘤患者中的可行性和疗效。

Feasibility and Efficacy of CD45RA+ Depleted Donor Lymphocytes Infusion After Haploidentical Transplantation With Post-Transplantation Cyclophosphamide in Patients With Hematological Malignancies.

机构信息

IRCCS Humanitas Research Hospital, Milan, Italy.

IRCCS Humanitas Research Hospital, Milan, Italy.

出版信息

Transplant Cell Ther. 2021 Jun;27(6):478.e1-478.e5. doi: 10.1016/j.jtct.2021.03.010. Epub 2021 Mar 11.

Abstract

Allogeneic stem cell transplantation from haploidentical donor using post-transplantation cyclophosphamide has been used to cure hematological diseases. Because of slow immunological reconstitution, there is an increased incidence of viral infection. The aim of our study was to prospectively evaluate the efficacy and the feasibility of a CD45RA+ depleted donor lymphocytes infusion (DLI) in terms of reduction of viral infection early after haploidentical transplantation. This a prospective single-center study. We enrolled 23 patients, of whom 19 were evaluable. Graft-versus-host disease (GVHD) prophylaxis was the same for all patients. The primary endpoint was 100-day cumulative incidence of viral infections. The primary endpoint was met, because the 100-day cumulative incidence of viral infection was 32%. The median time from transplantation to first CD45RA+ depleted DLI was 55 days (range, 46-63). 28% of patients had cytomegalovirus reactivation, no patients reactivated human herpesvirus-6; 1 patient developed BK virus related hemorrhagic cystitis. Most of the patients received the planned 3 infusions. Only 1 patient had development of grade 2 acute GVHD, and 2 patients had moderate chronic GVHD. All evaluable patients were off immunosuppressive therapy at last follow-up. The median follow-up was 12 months (range, 3-23), the 1-year overall survival and progression-free survival were 79% and 75%, respectively; the 100-day and 1-year non-relapse mortality were 5% and 12%, respectively. CD45RA+ depleted DLI are feasible in patients treated with haploidentical transplantation. The toxic profile is good with a low risk for development of both acute and chronic GVHD.

摘要

异基因造血干细胞移植(HSCT)使用移植后环磷酰胺(PT-Cy)已被用于治疗血液系统疾病。由于免疫重建缓慢,病毒感染的发生率增加。我们的研究旨在前瞻性评估 CD45RA+耗竭供者淋巴细胞输注(DLI)在减少异基因 HSCT 后早期病毒感染方面的疗效和可行性。这是一项前瞻性单中心研究。我们纳入了 23 例患者,其中 19 例可评估。所有患者的移植物抗宿主病(GVHD)预防方案相同。主要终点是异基因 HSCT 后 100 天累积病毒感染发生率。主要终点达到,因为病毒感染的 100 天累积发生率为 32%。从移植到首次 CD45RA+耗竭 DLI 的中位时间为 55 天(范围,46-63)。28%的患者发生巨细胞病毒(CMV)再激活,无患者发生人类疱疹病毒 6(HHV-6)再激活;1 例患者发生 BK 病毒相关出血性膀胱炎。大多数患者接受了计划的 3 次输注。只有 1 例患者出现 2 级急性 GVHD,2 例患者出现中度慢性 GVHD。所有可评估的患者在最后一次随访时均已停止免疫抑制治疗。中位随访时间为 12 个月(范围,3-23),1 年总生存率和无进展生存率分别为 79%和 75%;100 天和 1 年非复发死亡率分别为 5%和 12%。CD45RA+耗竭 DLI 可用于接受异基因 HSCT 治疗的患者。其毒性谱良好,发生急性和慢性 GVHD 的风险低。

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