Late effects after novel therapies for childhood cancer: Anticipating the future landscape of health outcomes for survivors

Amy M Berkman,David T Teachey,Matthew J Ehrhardt,Ching-Hon Pui,Hiroto Inaba,Seth E Karol,Sharon M Castellino,Stephanie B Dixon,Jun J Yang,Thomas G Gross,Sara M Federico,Roger J Packer,Alberto S Pappo,Ibrahim Qaddoumi,Ralph Salloum,Stephanie M Smith,Todd Cooper,Tara O Henderson,Douglas S Hawkins,Paul C Nathan,Eric J Chow,Elizabeth Fox,Gregory T Armstrong
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Abstract

Abstract Five-year survival rates for childhood cancer now exceed 85%, with recent improvements driven by advances in understanding of tumor biology allowing for molecular risk stratification. The introduction of novel therapies, including antibodies, antibody-drug conjugates, immune checkpoint inhibitors, cellular therapy, and targeted small molecule inhibitors into early-phase and pivotal trials has the potential to further improve survival. Although these agents have transformed outcomes for some children with cancer, their long-term toxicity profiles remain poorly defined. Large cohort studies have characterized the late effects of conventional cytotoxic chemotherapies and radiation, informing survivorship guidelines and risk-based surveillance strategies. In contrast, the distinct mechanisms of action of targeted and immune-based therapies introduce new and potentially persistent toxicities affecting cardiovascular, neurologic, endocrine, gastrointestinal, and immune systems. This review synthesizes current evidence on acute toxicities of novel therapies and summarizes available data about persistent long-term toxicities and new onset late effects outcomes, including growth impairment, persistent immune dysfunction, and subsequent malignancies in children treated with these agents. We focus on therapies with U.S. Food and Drug Administration approval for pediatric indications. Current evidence from acute toxicity profiles, limited pediatric long-term follow-up, and emerging data from adult populations highlights the urgent need for systematic evaluation of long-term outcomes in children treated with these therapies. As the use of novel agents continues to expand, extending established survivorship cohorts to include children exposed to novel therapies, while developing complementary approaches to detect previously unrecognized toxicities, will be essential for defining late effects and informing evidence-based surveillance and intervention strategies.
儿童癌症新疗法后的后期效应:预测幸存者健康结果的未来前景
儿童癌症的5年生存率现已超过85%,最近由于对肿瘤生物学的理解的进步,使得分子风险分层得以实现。新疗法的引入,包括抗体、抗体-药物偶联物、免疫检查点抑制剂、细胞疗法和靶向小分子抑制剂,在早期和关键试验中有可能进一步提高生存率。尽管这些药物已经改变了一些癌症儿童的预后,但它们的长期毒性特征仍然不明确。大型队列研究已经确定了传统细胞毒性化疗和放疗的晚期效应,为生存指南和基于风险的监测策略提供了信息。相比之下,靶向治疗和免疫治疗的不同作用机制引入了新的和潜在的持久性毒性,影响心血管、神经、内分泌、胃肠道和免疫系统。这篇综述综合了目前关于新疗法急性毒性的证据,并总结了关于持续长期毒性和新发迟发效应结局的现有数据,包括使用这些药物治疗的儿童的生长损害、持续免疫功能障碍和随后的恶性肿瘤。我们专注于美国食品和药物管理局批准的儿科适应症治疗。目前来自急性毒性特征、有限的儿科长期随访和来自成年人群的新数据的证据表明,迫切需要对接受这些疗法治疗的儿童的长期结果进行系统评估。随着新药物的使用不断扩大,扩大已建立的幸存者队列,包括接受新疗法的儿童,同时开发补充方法来检测以前未被认识到的毒性,对于确定晚期效应和告知循证监测和干预策略至关重要。
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