[Recent advances and future perspectives in the treatment of classical Hodgkin lymphoma].

Nobuhiko Yamauchi
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Abstract

Classical Hodgkin lymphoma (cHL) is a highly curable malignancy, with long-term remission achieved in approximately 85% of patients with limited-stage disease and in about 70% of those with advanced-stage disease following first-line therapy. In limited-stage cHL, treatment is generally guided by appropriate risk stratification, and the combination of ABVD followed by radiotherapy has long constituted the therapeutic backbone. For advanced-stage disease, six cycles of brentuximab vedotin plus AVD (BV-AVD) are currently regarded as the standard first-line treatment, whereas six cycles of ABVD remains a reasonable option for older patients in whom treatment tolerability is a particular concern. In recent years, the results of large-scale clinical trials evaluating first-line regimens incorporating brentuximab vedotin (BV) or immune checkpoint inhibitors (IO), together with interim PET-adapted treatment strategies, have shown promise for further improving treatment outcomes while minimizing the use of radiotherapy. For relapsed or refractory disease, immunotherapeutic approaches, including CD30-directed CAR T-cell therapy, are under active development. In parallel, circulating tumor DNA (ctDNA) is emerging as a promising biomarker for minimal residual disease assessment, and ctDNA-based molecular classification has also been proposed. This review outlines the current status and unresolved challenges of first-line treatment for cHL and discusses future perspectives in this evolving field.

经典霍奇金淋巴瘤治疗的最新进展和未来展望。
经典霍奇金淋巴瘤(cHL)是一种高度可治愈的恶性肿瘤,在一线治疗后,约85%的有限期患者和约70%的晚期患者实现了长期缓解。在有限期cHL中,治疗通常以适当的风险分层为指导,ABVD联合放疗长期以来一直是治疗的支柱。对于晚期疾病,6个周期的brentuximab vedotin加AVD (BV-AVD)目前被认为是标准的一线治疗,而6个周期的ABVD对于治疗耐受性特别关注的老年患者仍然是一个合理的选择。近年来,大规模临床试验的结果评估了一线方案,包括brentuximab vedotin (BV)或免疫检查点抑制剂(IO),以及临时pet适应治疗策略,显示出进一步改善治疗结果的希望,同时最大限度地减少了放疗的使用。对于复发或难治性疾病,包括cd30导向的CAR - t细胞疗法在内的免疫治疗方法正在积极发展中。与此同时,循环肿瘤DNA (ctDNA)正在成为一种有前景的生物标志物,用于最小残留疾病评估,基于ctDNA的分子分类也被提出。本文概述了cHL一线治疗的现状和未解决的挑战,并讨论了这一不断发展的领域的未来前景。
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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