研究概要
CR患者在第31个月随访时生长规律,另一例PD患者在治疗后20个月仍存活并正在接受化疗。
中文摘要
尽管发病率低,神经母细胞瘤作为一种免疫冷肿瘤,是儿科最常见的颅外实体肿瘤。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)细胞对肿瘤细胞的细胞毒性作用不依赖于抗原呈递细胞和适应性免疫系统。本试验的主要终点是评估在auto-HSCT后对复发/难治性神经母细胞瘤患者注射异体、体外扩增并致敏的NK细胞的安全性。次要终点包括该干预控制肿瘤的疗效。NK细胞在符合GMP标准的CliniMACS系统中被分离并体外致敏(通过添加白细胞介素[IL]-2、IL-15和IL-21),并给予四例复发/难治性MYCN阳性神经母细胞瘤患者。NK细胞注射(首次和第二次注射分别为1和5 10 7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,观察到一例完全缓解(CR)和一例部分缓解(PR),而两例表现为疾病进展(PD)。在随访评估中,两例因疾病进展死亡,包括那例PR病例。CR患者在31个月随访时生长发育正常,另一例PD患者在治疗后20个月仍存活并正在接受化疗。该疗法是HSCT后管理难治性神经母细胞瘤的一种有吸引力且可行的方法。需要进一步研究探索其在高危神经母细胞瘤和其他免疫冷肿瘤中以更高剂量和更频繁给药方案的疗效。试验注册号:irct.behdasht.gov。ir(伊朗临床试验注册中心,编号 IRCT20201202049568N1)。
展开英文摘要原文
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 7 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).
论文信息
- 作者
- Mohseni R、Mahdavi Sharif P、Behfar M、Shojaei S、Shoae-Hassani A、Jafari L、Khosravi A、Nikfetrat Z
- 第一作者单位
- Pediatric Cell and Gene Therapy Research Center, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Tehran, 14194, Iran.Iran
- 通讯作者单位
- Pediatric Cell and Gene Therapy Research Center, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Tehran, 14194, Iran. aahamidieh@tums.ac.ir.Iran
- 文献类型
- I 期临床试验
- 期刊
- Scientific reports2024 Sep 9