Late Adverse Effects after Treatment for Childhood Acute Leukemia

Q3 Medicine Acta medica academica Pub Date : 2024-04-15 DOI:10.5644/ama2006-124.438
Jelena Roganovic, Riccardo Haupt, E. Bárdi, L. Hjorth, Gisela Michel, Vesna Pavasovic, Katrin Scheinemann, H. V. D. van der Pal, L. Zadravec Zaletel, Ana E. Amariutei, Roderick Skinner, PanCare Board
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Abstract

The aim of this review is to raise awareness and knowledge among healthcare professionals and policymakers about late adverse effects in survivors of childhood leukemia. With contemporary treatment, over 90% of children with acute lymphoblastic leukemia (ALL) and over 60% with acute myeloid leukemia (AML) are cured. Large cohort studies demonstrate that 20% of ALL and most AML survivors have at least one chronic health condition by 20-25 years after diagnosis. These are life-changing or threatening in some survivors and contribute to increased premature mortality. We describe the frequency, causes, clinical features, and natural history of the most frequent and severe late adverse effects in childhood leukemia survivors, including subsequent malignant neoplasms, metabolic toxicity, gonadotoxicity and impaired fertility, endocrinopathy and growth disturbances, bone toxicity, central and peripheral neurotoxicity, cardiotoxicity, psychosocial late effects, accelerated ageing and late mortality. The wide range of late effects in survivors of haemopoietic stem cell transplant is highlighted. Recent developments informing the approach to long-term survivorship care are discussed, including electronic personalized patient-specific treatment summaries and care plans such as the Survivor Passport (SurPass), surveillance guidelines and models of care. The importance of ongoing vigilance is stressed given the increasing use of novel targeted drugs with limited experience of long-term outcomes. Conclusion. It is vital to raise awareness of the existence and severity of late effects of childhood leukemia therapy among parents, patients, health professionals, and policymakers. Structured long-term surveillance recommendations are necessary to standardize follow-up care.
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儿童急性白血病治疗后的晚期不良反应
本综述旨在提高医护人员和决策者对儿童白血病幸存者晚期不良反应的认识和了解。通过现代治疗方法,90% 以上的急性淋巴细胞白血病(ALL)患儿和 60% 以上的急性髓细胞白血病(AML)患儿可以治愈。大型队列研究表明,20% 的急性淋巴细胞白血病(ALL)和大多数急性髓细胞白血病(AML)幸存者在确诊后 20-25 年间至少患有一种慢性疾病。这些病症改变了一些幸存者的生活或对其构成威胁,并导致过早死亡率上升。我们描述了儿童白血病幸存者最常见和最严重的晚期不良反应的频率、原因、临床特征和自然史,包括后续恶性肿瘤、代谢毒性、性腺毒性和生育能力受损、内分泌病变和生长障碍、骨毒性、中枢和外周神经毒性、心脏毒性、心理社会晚期反应、加速衰老和晚期死亡率。重点介绍了造血干细胞移植幸存者的各种晚期效应。讨论了长期幸存者护理方法的最新进展,包括电子个性化患者治疗摘要和护理计划(如幸存者护照(SurPass))、监测指南和护理模式。鉴于新型靶向药物的使用越来越多,但长期疗效经验有限,因此强调了持续警惕的重要性。结论。提高家长、患者、医疗专业人员和政策制定者对儿童白血病治疗后期效应的存在和严重性的认识至关重要。有必要提出结构化的长期监测建议,以规范后续治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta medica academica
Acta medica academica Medicine-Medicine (all)
CiteScore
1.90
自引率
0.00%
发文量
21
审稿时长
15 weeks
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