Personalized medicine for Hodgkin lymphoma: Mitigating toxicity while preserving cure

Hematol Oncol. 2021 Jun:39 Suppl 1:39-45. doi: 10.1002/hon.2856.

Abstract

The treatment of classical Hodgkin lymphoma in young patients is one of the success stories of modern medicine. The use of risk- and response-adapted approaches to guide treatment decisions has led to impressive cure rates while reducing the long-term toxicity associated with more intensive therapies. Tissue biomarkers have not yet proven more effective than clinical characteristics for risk stratification of patients at presentation, but functional imaging features such as metabolic tumor volume may be used to predict response, if early observations can be validated. The success of treatment in younger patients has unfortunately not been mirrored in those over 60, where complex decision-making is often required, with a paucity of data from clinical trials. The use of PD1 blocking antibodies and brentuximab vedotin in this cohort, either alone or in combination with chemotherapy, may provide attractive options. The incorporation of frailty assessment, quality-of-life outcomes, and specialist geriatric input is also important to ensure the best outcomes for this diverse group.

Keywords: FDG-PET; Hodgkin lymphoma; antibody-drug conjugate; checkpoint blocking antibody.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor* / antagonists & inhibitors
  • Biomarkers, Tumor* / genetics
  • Biomarkers, Tumor* / metabolism
  • Brentuximab Vedotin / therapeutic use*
  • Female
  • Hodgkin Disease* / drug therapy
  • Hodgkin Disease* / genetics
  • Hodgkin Disease* / metabolism
  • Hodgkin Disease* / pathology
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use*
  • Male
  • Middle Aged
  • Neoplasm Proteins* / antagonists & inhibitors
  • Neoplasm Proteins* / genetics
  • Neoplasm Proteins* / metabolism
  • Precision Medicine*
  • Programmed Cell Death 1 Receptor* / antagonists & inhibitors
  • Programmed Cell Death 1 Receptor* / genetics
  • Programmed Cell Death 1 Receptor* / metabolism

Substances

  • Biomarkers, Tumor
  • Immune Checkpoint Inhibitors
  • Neoplasm Proteins
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Brentuximab Vedotin