Immunotherapy-Based Therapies in Pediatric Hodgkin Lymphoma: Potential to Narrow the Gap in Long-Term Survival

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ID: 330738
2026
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Abstract
Abstract Pediatric advanced-stage Hodgkin lymphoma (HL) is highly curable, yet survivors treated with historical regimens face substantial late morbidity and excess mortality. Immunotherapy-based frontline therapies improve disease control, but late toxicities remain unknown. We developed a simulation model to project lifetime outcomes after contemporary brentuximab vedotin- or nivolumab-containing regimens using trial data (COG AHOD1331 and SWOG S1826), Childhood Cancer Survivor Study data, and national databases. We assessed how frontline and relapse therapy changes could influence long-term survival and late-effect outcomes, with sensitivity analyses to evaluate potential immunotherapy-related late mortality. Compared with expected survival at age 50 in the general population, HL survival was 86% at age 50 after historical regimens and 92-93% after contemporary immunotherapy-based therapies. Survival gains persisted unless immunotherapy-related late mortality exceeded approximately 8%. These projections suggest contemporary regimens may narrow the long-term survival gap while reducing late-effect burden.
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openalex_W7215071976 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Jenna R. Rogers, Zachary J. Ward, Angela Marie Feraco, Sharon M. Castellino, Kayla L. Stratton, Wendy M. Leisenring, Gregory T. Armstrong, Eric Jessen Chow, Rebecca M. Howell, Melissa M. Hudson, Kara M. Kelly, Lindsay McOmber Morton, Kevin Charles Oeffinger, Susan A. Smith, Lisa Diller, Jennifer M. Yeh
Journal JNCI Journal of the National Cancer Institute
Year 2026
DOI
10.1093/jnci/djag353
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