Translational Research in Pediatric Oncology, Hematopoietic Transplantation & Cell Therapy, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Pediatric Hemato-Oncology Unit, Hospital Universitario La Paz, Madrid, Spain.
Cancer Lett. 2018 May 28;422:107-117. doi: 10.1016/j.canlet.2018.02.033. Epub 2018 Feb 23.
Primary refractory or relapsed pediatric leukemia yield significant morbidity and mortality, with long-term survival rates <40%. Here we present a post-hoc analysis assessing safety and efficacy of infusing activated and expanded Natural Killer cells (NKAE) from haploidentical donors in patients from 2 clinical trials. In total, 18 children, adolescents and young adults with relapse or refractory acute leukemia were treated with two cycles of rescue chemotherapy followed by fresh NKAE cells infusions and low doses of IL-2. The overall response rate, complete remission achievement at the end of the study, was 72% (13 of 18). We infused 52 NKAE cell products containing a median of 6.76 × 10 NK cells/kg (0.7-34.16) and 0.49 × 10 T cells/kg (0-11). All infusions were well tolerated with no graft versus host disease nor other serious adverse events. Among the 14 patients who completed treatment, 4 of them are alive and leukemia-free more than 750 days post-transplant. We conclude that infusion of fresh NKAE cell therapy is feasible and safe in heavily pretreated pediatric population, and should be further investigated in advanced-phase clinical trials as well as a consolidation therapy to decrease relapse in patients with high-risk leukemia.
Registered at www.clinicaltrials.gov as NCT01944982 and NCT02074657.
原发性难治或复发性儿科白血病导致显著的发病率和死亡率,长期生存率<40%。在这里,我们进行了一项事后分析,评估来自半相合供体的激活和扩增的自然杀伤细胞(NKAE)输注在 2 项临床试验中的患者的安全性和疗效。共有 18 名患有复发或难治性急性白血病的儿童、青少年和年轻成人接受了两个周期的挽救性化疗,随后输注新鲜 NKAE 细胞和低剂量的 IL-2。总的来说,18 名患者中有 13 名(72%)对治疗有反应,在研究结束时达到完全缓解。我们输注了 52 个 NKAE 细胞产品,其中包含中位数为 6.76×10 NK 细胞/kg(0.7-34.16)和 0.49×10 T 细胞/kg(0-11)。所有输注均耐受良好,无移植物抗宿主病或其他严重不良事件。在完成治疗的 14 名患者中,有 4 名患者在移植后超过 750 天白血病无复发且存活。我们得出结论,新鲜 NKAE 细胞疗法输注在预处理过的儿科人群中是可行且安全的,应在高级临床试验中进一步研究,作为巩固治疗以降低高危白血病患者的复发率。
在 www.clinicaltrials.gov 上注册为 NCT01944982 和 NCT02074657。