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小儿复发性或难治性急性淋巴细胞白血病I期和II期试验中的研究性治疗方案。

Investigational treatment options in phase I and phase II trials for relapsed or refractory acute lymphoblastic leukemia in pediatric patients.

作者信息

Asare Julie M, Rabik Cara A, Muller Bradley, Brown Patrick A, Cooper Stacy

机构信息

Department of Oncology, The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Expert Opin Investig Drugs. 2021 Jun;30(6):611-620. doi: 10.1080/13543784.2021.1916466. Epub 2021 May 4.

Abstract

: Upfront treatment of pediatric patients with B-cell acute lymphoblastic leukemia (B-ALL) and T-cell acute lymphoblastic leukemia (T-ALL) results in cure rates of 60-95%, depending on risk factors. However, patients with refractory or relapsed B-ALL or T-ALL have much worse outcomes with conventional chemotherapy, hence treatment of these cohorts with novel agents is a priority.: This paper reviews early phase clinical trials in pediatric leukemia. Investigational antibody therapy, chimeric antigen receptor T-cell (CAR-T), and other targeted therapies are examined. The authors discuss the mechanisms of action, side effects, trial designs, and outcomes and reflect on potential research directions. PubMed and Clinicaltrials.gov were searched from 2010 to present, using keywords 'lymphoblastic leukemia' with filters for pediatric age, Phase 1 clinical trial and Phase 2 clinical trial.: Pediatric patients with relapsed or refractory leukemia often do not derive additional benefit from intensified conventional chemotherapy approaches which have arguably been maximized in the upfront setting. Therefore, novel approaches, such as immunotherapy and targeted agents should be prioritized. Progress will require commitment from pharmaceutical companies regarding these orphan diagnoses and acknowledgment from regulatory bodies that outcomes are suboptimal with conventional chemotherapy.

摘要

对患有B细胞急性淋巴细胞白血病(B-ALL)和T细胞急性淋巴细胞白血病(T-ALL)的儿科患者进行前期治疗,根据风险因素不同,治愈率可达60%-95%。然而,患有难治性或复发性B-ALL或T-ALL的患者采用传统化疗的预后要差得多,因此,用新型药物治疗这些患者群体是当务之急。本文综述了儿科白血病的早期临床试验。研究了研究性抗体疗法、嵌合抗原受体T细胞(CAR-T)及其他靶向疗法。作者讨论了其作用机制、副作用、试验设计及结果,并思考了潜在的研究方向。检索了2010年至今的PubMed和Clinicaltrials.gov,使用关键词“淋巴细胞白血病”,并筛选儿科年龄、1期临床试验和2期临床试验。患有复发性或难治性白血病的儿科患者通常无法从强化的传统化疗方法中获得额外益处,而传统化疗方法在前瞻性治疗中可能已达到最大化。因此,应优先考虑免疫疗法和靶向药物等新型方法。取得进展需要制药公司对这些罕见病诊断给予支持,以及监管机构承认传统化疗的疗效并不理想。

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