Allogeneic stem cell transplantation with prior pembrolizumab and bendamustine therapy induce complete metabolic response in relapsed/refractory classical hodgkin lymphoma with relapse after nivolumab
Relapsed/refractory classical Hodgkin lymphoma (r/r cHL) poses a therapeutic challenge, particularly after failure of checkpoint inhibitors (CPIs) and brentuximab vedotin. We report a case of a heavily pretreated young male patient with r/r cHL who achieved complete metabolic response (CMR) after allogeneic hematopoietic stem cell transplantation (allo-HCT) following pembrolizumab and bendamustine therapy, currently in CMR at 19 months post-transplantation. Despite prior resistance to nivolumab, pembrolizumab combined with bendamustine contributed to disease control in the pre-transplant period. This case highlights allo-HCT's curative potential even in partial responders and suggests that pre-transplant CPI therapy may enhance the graft-versus-lymphoma effect, improving post-transplantation outcomes in r/r cHL. Another explanation for the therapeutic success may be that the employment of a CPI has likely contributed to sensitization to chemotherapy and bendamustine potentially lowering the occurrence of GvHD due to T-cell compartment impairment, with the need for large scale prospective trials to demonstrate our findings.
Authors
- Jarosław Dybko (ORCID: https://orcid.org/0000-0003-3555-2887)
- Zbigniew Podgajny
- Monika Mordak‐Domagała
- Agnieszka Kuś
- Ugo Giordano (ORCID: https://orcid.org/0009-0000-8735-3076)
- Karolina Kędziora
- Mateusz Sawicki
- Zuzanna Dybko
Institutions
- Wrocław University of Science and Technology (PL)
- Wroclaw Medical University (PL)
- Affidea (CH)
- Wroclaw University of Health and Sport Sciences (PL)
- Cells Therapy (Poland) (PL)
- AGH University of Krakow (PL)
Publication Details
- Journal
- Annals of Hematology
- Published
- 2025-08-30
- DOI
- https://doi.org/10.1007/s00277-025-06568-8
- Primary Topic
- Lymphoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00