Evens Andrew M
Division of Blood Disorders, Rutgers Cancer Institute, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Hematol Oncol. 2025 Jun;43 Suppl 2(Suppl 2):e70066. doi: 10.1002/hon.70066.
The treatment landscape for newly diagnosed classical Hodgkin lymphoma (cHL) has seen remarkable advancements over the past decade, which have been fueled by improved prognostication and response-adapted techniques, and primarily driven by randomized clinical trials, especially via the incorporation of novel targeted therapeutic agents into frontline therapy. The studies include several recent landmark clinical trials that integrated novel targeted therapeutic agents into frontline therapy for adolescents and adults with cHL. For early-stage disease, the completion of PET-based response-adapted studies has resulted in refined therapeutic approaches, particularly informing the amount and type of chemotherapy as well as the impact of radiotherapy, balancing immediate efficacy with the mitigation of post-acute and long-term consequences. In untreated advanced-stage cHL, the integration of brentuximab vedotin and checkpoint inhibitors has ushered in a new therapeutic era with improved patient outcomes with progressive-free survival rates exceeding 90%. In addition, outcomes have significantly improved for older cHL patients, partly due to the understanding of the unique needs of this patient population (e.g., the impact of geriatric assessments) and vis-à-vis frontline regimens that have incorporated targeted therapeutic agents. Future directions in cHL emphasize the need for prospective clinical trials that include dynamic clinical prediction models, metabolic tumor burden, ctDNA, and other critical biomarkers to establish predictive factors of treatment effect that yield individualized therapeutic options for patients. Continued innovations in frontline therapy, coupled with efforts to address unmet needs in specific populations, promise to enhance survival rates further and preserve long-term quality of life for all individuals with cHL.
在过去十年中,新诊断的经典型霍奇金淋巴瘤(cHL)的治疗格局取得了显著进展,这得益于预后评估和适应性治疗技术的改进,主要由随机临床试验推动,特别是通过将新型靶向治疗药物纳入一线治疗。这些研究包括最近的几项具有里程碑意义的临床试验,这些试验将新型靶向治疗药物纳入了青少年和成人cHL的一线治疗。对于早期疾病,基于PET的适应性反应研究的完成带来了更精细的治疗方法,特别是在化疗的剂量和类型以及放疗的影响方面提供了指导,在平衡即时疗效与减轻急性和长期后果之间取得了平衡。在未经治疗的晚期cHL中,将维布妥昔单抗和检查点抑制剂相结合开创了一个新的治疗时代,患者预后得到改善,无进展生存率超过90%。此外,老年cHL患者的预后也有显著改善,部分原因是对该患者群体独特需求的认识(例如老年评估的影响)以及针对纳入靶向治疗药物的一线治疗方案。cHL的未来发展方向强调需要进行前瞻性临床试验,包括动态临床预测模型、代谢肿瘤负荷、ctDNA和其他关键生物标志物,以建立治疗效果的预测因素,为患者提供个性化治疗选择。一线治疗的持续创新,加上满足特定人群未满足需求的努力,有望进一步提高生存率,并为所有cHL患者保留长期生活质量。