Remission of relapsed/refractory classical Hodgkin lymphoma induced by brentuximab vedotin and pembrolizumab combination after allogeneic hematopoietic stem cell transplantation: a case report

Front Immunol. 2024 Mar 6:15:1360275. doi: 10.3389/fimmu.2024.1360275. eCollection 2024.

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative treatment option for patients with highly chemorefractory Hodgkin lymphoma (HL). The CD30-targeting antibody-drug conjugate Brentuximab-Vedotin (BV) and programmed cell death protein-1 (PD-1) blocking agents have demonstrated clinical activity with durable responses in relapsed/refractory (r/r) HL. However, patients with a history of allo-HSCT were frequently excluded from clinical trials due to concerns about the risk of graft-versus-host disease (GVHD). We report the clinical history of a patient with refractory classical HL who underwent two allo-HSCTs (first from matched unrelated and second from haploidentical donor) after relapsing on BV and nivolumab and for whom durable remission was finally obtained using BV-pembrolizumab combination for relapse after haploidentical HSCT. Such treatment was associated with the onset of GVHD after only two cycles which led to treatment discontinuation. However, the side effects were rapidly controlled, and after 2 years of follow-up, the patient is still in remission. Our data support the feasibility and efficacy of combining PD-1 blockade with BV to enhance the graft-versus-lymphoma effect after allo-HSCT.

Keywords: DLI; Hodgkin lymphoma; brentuximab-vedotin; haploidentical allogeneic stem cell transplant; pembrolizumab.

Publication types

  • Case Reports

MeSH terms

  • Antibodies, Monoclonal, Humanized*
  • Brentuximab Vedotin / therapeutic use
  • Graft vs Host Disease* / drug therapy
  • Graft vs Host Disease* / etiology
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Hodgkin Disease* / drug therapy
  • Humans
  • Neoplasm Recurrence, Local / drug therapy
  • Programmed Cell Death 1 Receptor

Substances

  • Brentuximab Vedotin
  • pembrolizumab
  • Programmed Cell Death 1 Receptor
  • Antibodies, Monoclonal, Humanized

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.