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自体造血干细胞移植后复发/难治性神经母细胞瘤异体自然杀伤细胞治疗的安全性和疗效的 I 期研究。

Phase I study of safety and efficacy of allogeneic natural killer cell therapy in relapsed/refractory neuroblastomas post autologous hematopoietic stem cell transplantation.

机构信息

Pediatric Cell and Gene Therapy Research Center, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Tehran, 14194, Iran.

National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.

出版信息

Sci Rep. 2024 Sep 9;14(1):20971. doi: 10.1038/s41598-024-70958-7.

Abstract

Despite low incidence, neuroblastoma, an immunologically cold tumor, is the most common extracranial solid neoplasm in pediatrics. In relapsed/refractory cases, the benefits of autologous hematopoietic stem cell transplantation (auto-HSCT) and other therapies are limited. Natural killer (NK) cells apply cytotoxicity against tumor cells independently of antigen-presenting cells and the adaptive immune system. The primary endpoint of this trial was to assess the safety of the injection of allogenic, ex vivo-expanded and primed NK cells in relapsed/refractory neuroblastoma patients after auto-HSCT. The secondary endpoint included the efficacy of this intervention in controlling tumors. NK cells were isolated and primed ex vivo (by adding interleukin [IL]-2, IL-15, and IL-21) in a GMP-compliant CliniMACS system and administered to four patients with relapsed/refractory MYCN-positive neuroblastoma. NK cell injections (1 and 5 × 10 cells/kg in the first and second injections, respectively) were safe, and no acute or sub-acute adverse events were observed. During the follow-up period, one complete response (CR) and one partial response (PR) were observed, while two cases exhibited progressive disease (PD). In follow-up evaluations, two died due to disease progression, including the case with a PR. The patient with CR had regular growth at the 31-month follow-up, and another patient with PD is still alive and receiving chemotherapies 20 months after therapy. This therapy is an appealing and feasible approach for managing refractory neuroblastomas post-HSCT. Further studies are needed to explore its efficacy with higher doses and more frequent administrations for high-risk neuroblastomas and other immunologically cold tumors.Trial registration number: irct.behdasht.gov.ir (Iranian Registry of Clinical Trials, No. IRCT20201202049568N1).

摘要

尽管神经母细胞瘤的发病率较低,但它是儿科中最常见的颅外实体瘤,属于免疫原性冷肿瘤。在复发/难治性病例中,自体造血干细胞移植(auto-HSCT)和其他疗法的获益有限。自然杀伤(NK)细胞独立于抗原呈递细胞和适应性免疫系统,通过细胞毒性作用杀伤肿瘤细胞。本试验的主要终点是评估在自体 HSCT 后,对复发/难治性神经母细胞瘤患者注射同种异体、体外扩增和预致敏 NK 细胞的安全性。次要终点包括该干预措施控制肿瘤的疗效。NK 细胞在符合 GMP 的 CliniMACS 系统中体外分离和预致敏(通过添加白细胞介素[IL]-2、IL-15 和 IL-21),并用于 4 例 MYCN 阳性神经母细胞瘤复发/难治性患者。NK 细胞注射(第 1 次和第 2 次分别为 1 和 5×10 个细胞/kg)是安全的,未观察到急性或亚急性不良事件。在随访期间,观察到 1 例完全缓解(CR)和 1 例部分缓解(PR),而 2 例发生进展性疾病(PD)。在随访评估中,2 例因疾病进展而死亡,包括 PR 病例。CR 患者在 31 个月的随访中生长正常,另 1 例 PD 患者在治疗后 20 个月仍存活并接受化疗。这种治疗方法对于管理 HSCT 后难治性神经母细胞瘤具有吸引力和可行性。需要进一步研究以探索更高剂量和更频繁给药对高危神经母细胞瘤和其他免疫原性冷肿瘤的疗效。试验注册号:irct.behdasht.gov.ir(伊朗临床试验注册中心,编号 IRCT20201202049568N1)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/11385932/62f5a961a4ae/41598_2024_70958_Fig1_HTML.jpg

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