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利用免疫疗法治疗小儿 T 细胞恶性肿瘤。

Harnessing immunotherapy for pediatric T-cell malignancies.

机构信息

Division of Oncology, Department of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia and Pereleman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Expert Rev Clin Immunol. 2020 Apr;16(4):361-371. doi: 10.1080/1744666X.2020.1732819. Epub 2020 Feb 27.

Abstract

Pediatric T-cell hematologic malignancies are a diverse group of rare cancers. The most common pediatric T-cell malignancies include T-cell acute lymphoblastic leukemia (T-ALL) and anaplastic large cell lymphoma (ALCL). Although the overall survival rates have improved markedly in recent years, children with relapsed T-ALL and ALCL have very low rates of cure and few salvage therapies exist. Current treatment regimens rely on toxic chemotherapies with significant short- and long-term morbidity. Immunotherapies, including antibodies and adoptive cellular therapies, have revolutionized the treatment of B-cell malignancies in pediatrics. The adaptation of these therapies to T-cell malignancies has been slower because of challenges implicit in the design and implementation of immunotherapies for T-cell malignancies, including the potential risks of fratricide, immunosuppression, and graft versus host disease (GVHD). We present a review of current challenges in the development of immunotherapies for T-cell hematologic malignancies, potential solutions and therapies under investigation. We include a particular focus on T-ALL and ALCL. Immunotherapies offer promising strategies to improve outcomes in children with T-cell malignancies, particularly in the setting of relapse. Optimizing efficacy, mitigating toxicity, and safely integrating with conventional therapies are key considerations as immunotherapies are translated into the clinic.

摘要

儿科 T 细胞血液恶性肿瘤是一组多样化的罕见癌症。最常见的儿科 T 细胞恶性肿瘤包括 T 细胞急性淋巴细胞白血病(T-ALL)和间变大细胞淋巴瘤(ALCL)。尽管近年来整体生存率有了显著提高,但复发的 T-ALL 和 ALCL 患儿的治愈率非常低,且几乎没有挽救疗法。目前的治疗方案依赖于具有明显短期和长期发病率的毒性化疗。免疫疗法,包括抗体和过继细胞疗法,已经彻底改变了儿科 B 细胞恶性肿瘤的治疗。由于设计和实施 T 细胞恶性肿瘤免疫疗法中存在的挑战,包括同种杀伤、免疫抑制和移植物抗宿主病(GVHD)的潜在风险,这些疗法在 T 细胞恶性肿瘤中的应用速度较慢。我们介绍了当前 T 细胞血液恶性肿瘤免疫疗法发展所面临的挑战,以及正在研究的潜在解决方案和疗法。我们特别关注 T-ALL 和 ALCL。免疫疗法为改善 T 细胞恶性肿瘤患儿的预后提供了有前途的策略,特别是在复发的情况下。在将免疫疗法转化为临床应用时,优化疗效、减轻毒性以及安全地与常规疗法结合是关键考虑因素。

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