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2023 年复发型儿科急性髓系白血病的研究现状。

Relapsed pediatric acute myeloid leukaemia: state-of-the-art in 2023.

机构信息

Division of Haematology/Oncology, The Hospital for Sick Children, Department of Paediatrics, University of Toronto; Toronto, Ontario.

Division of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Pennsylvania, United States; University of Pennsylvania Perelman School of Medicine and Abramson Cancer Center; Philadelphia, Pennsylvania.

出版信息

Haematologica. 2023 Sep 1;108(9):2275-2288. doi: 10.3324/haematol.2022.281106.

DOI:10.3324/haematol.2022.281106
PMID:36861399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10483345/
Abstract

Although outcomes of children and adolescents with newly diagnosed acute myeloid leukemia (AML) have improved significantly over the past two decades, more than one-third of patients continue to relapse and experience suboptimal long-term outcomes. Given the small numbers of patients with relapsed AML and historical logistical barriers to international collaboration including poor trial funding and drug availability, the management of AML relapse has varied among pediatric oncology cooperative groups with several salvage regimens utilized and a lack of universally defined response criteria. The landscape of relapsed pediatric AML treatment is changing rapidly, however, as the international AML community harnesses collective knowledge and resources to characterize the genetic and immunophenotypic heterogeneity of relapsed disease, identify biological targets of interest within specific AML subtypes, develop new precision medicine approaches for collaborative investigation in early-phase clinical trials, and tackle challenges of universal drug access across the globe. This review provides a comprehensive overview of progress achieved to date in the treatment of pediatric patients with relapsed AML and highlights modern, state-of-the-art therapeutic approaches under active and emerging clinical investigation that have been facilitated by international collaboration among academic pediatric oncologists, laboratory scientists, regulatory agencies, pharmaceutical partners, cancer research sponsors, and patient advocates.

摘要

尽管过去二十年中,新诊断为急性髓细胞白血病(AML)的儿童和青少年的治疗结果已显著改善,但仍有超过三分之一的患者会复发,并经历不理想的长期预后。鉴于复发 AML 患者数量较少,以及历史上存在的国际合作障碍,包括试验资金不足和药物供应有限,儿科肿瘤学合作组在治疗 AML 复发时采用了多种挽救方案,并且缺乏普遍定义的反应标准。然而,随着国际 AML 界利用集体知识和资源来描述复发疾病的遗传和免疫表型异质性,确定特定 AML 亚型内感兴趣的生物学靶点,开发新的精准医学方法以在早期临床试验中进行合作研究,并解决全球范围内普遍药物获取的挑战,复发儿童 AML 的治疗格局正在迅速变化。这篇综述全面概述了在治疗复发 AML 儿童患者方面取得的进展,并重点介绍了在学术儿科肿瘤学家、实验室科学家、监管机构、制药合作伙伴、癌症研究赞助商和患者权益倡导者之间开展的国际合作的推动下,目前正在积极和新兴临床试验中研究的现代、最先进的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc1/10483345/f1d8cde7fd42/1082275.fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc1/10483345/54c821e98088/1082275.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc1/10483345/f1d8cde7fd42/1082275.fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc1/10483345/54c821e98088/1082275.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc1/10483345/f1d8cde7fd42/1082275.fig2.jpg

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