Anti–programmed cell death protein 1–based salvage therapy for relapsed/refractory Hodgkin lymphoma: a multicenter real-world analysis

In relapsed/refractory classic Hodgkin lymphoma (r/r cHL), salvage followed by high-dose chemotherapy and autologous stem cell transplantation (HD-ASCT) yields suboptimal outcomes. PD-1 inhibitor-based salvage regimens have shown superior complete response (CR) rates of up to 95% (for P-GVD) with unprecedented PFS after HD-ASCT. However, immune checkpoint inhibitors are not EMA-approved in 2nd line, and European data remain sparse. This retrospective, multicentric analysis included r/r cHL patients who received salvage with intent to consolidation. Response before and after SCT consolidation, and PFS and OS were assessed. 47 patients were included (median prior lines: 2). Salvage regimens were PD-1 monotherapy (n=10), PD-1 + chemotherapy [P-ICE/ N-ICE /P-GVD] (n=34), or PD-1 + BV (brentuximab vedotin) (n=3). Overall response (OR)/CR were 90.9%/47.7%. OR/CR rates by salvage regimen were: PD-1 monotherapy 80/10%; PD-1 + chemotherapy, 93.6/61.3%; PD-1 + BV, 100/33.3%. With median follow-up of 16 months, 1- year PFS was 83.9% and OS was 95.6%. In the subgroup of patients with one prior line (n=22), 1-year PFS was 100%. In this real-world cohort, previously reported high CR rates were not reached. However, with the restriction of a limited follow-up, outcomes after HDASCT were excellent, supporting the role of PD-1 inhibitor-based salvage followed by consolidative HD-ASCT for r/r cHL.

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Journal
Haematologica
Published
2026-02-26
DOI
https://doi.org/10.3324/haematol.2025.288996
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Anti–programmed cell death protein 1–based salvage therapy for relapsed/refractory Hodgkin lymphoma: a multicenter real-world analysis

Markus Sellmayr, Joe Puthenparambil, Justin Ferdinandus, Tanja Zamrik et al.
Haematologica
Lymphoma Diagnosis and Treatment
article

Anti–programmed cell death protein 1–based salvage therapy for relapsed/refractory Hodgkin lymphoma: a multicenter real-world analysis

Markus Sellmayr, Joe Puthenparambil, Justin Ferdinandus, Tanja Zamrik, Ina Bühnen, David Beverungen, Ulf Schnetzke, Hishan Tharmaseelan, Johannes C. Hellmuth, T. Melchardt, Evgenii Shumilov, Julia Meißner, Carsten Kobe, Lisa Marie Sgonina, Andrea Kerkhoff, Bastian Von Tresckow, Peter Borchmann, Paul J. Bröckelmann
article en

Abstract

In relapsed/refractory classic Hodgkin lymphoma (r/r cHL), salvage followed by high-dose chemotherapy and autologous stem cell transplantation (HD-ASCT) yields suboptimal outcomes. PD-1 inhibitor-based salvage regimens have shown superior complete response (CR) rates of up to 95% (for P-GVD) with unprecedented PFS after HD-ASCT. However, immune checkpoint inhibitors are not EMA-approved in 2nd line, and European data remain sparse. This retrospective, multicentric analysis included r/r cHL patients who received salvage with intent to consolidation. Response before and after SCT consolidation, and PFS and OS were assessed. 47 patients were included (median prior lines: 2). Salvage regimens were PD-1 monotherapy (n=10), PD-1 + chemotherapy [P-ICE/ N-ICE /P-GVD] (n=34), or PD-1 + BV (brentuximab vedotin) (n=3). Overall response (OR)/CR were 90.9%/47.7%. OR/CR rates by salvage regimen were: PD-1 monotherapy 80/10%; PD-1 + chemotherapy, 93.6/61.3%; PD-1 + BV, 100/33.3%. With median follow-up of 16 months, 1- year PFS was 83.9% and OS was 95.6%. In the subgroup of patients with one prior line (n=22), 1-year PFS was 100%. In this real-world cohort, previously reported high CR rates were not reached. However, with the restriction of a limited follow-up, outcomes after HDASCT were excellent, supporting the role of PD-1 inhibitor-based salvage followed by consolidative HD-ASCT for r/r cHL.

Haematologica
Heidelberg University (DE), Paracelsus Medical University (AT), LMU Klinikum (DE), Düsseldorf University Hospital (DE), Integrated Oncology (United States) (US), University Hospital Münster (DE), Essen University Hospital (DE), University Hospital Leipzig (DE), Jena University Hospital (DE), University Hospital Cologne (DE), West German Heart and Vascular Center Essen (DE), Heinrich Heine University Düsseldorf (DE), Ludwig-Maximilians-Universität München (DE)
Amgen, Bristol-Myers Squibb, Eli Lilly and Company, AstraZeneca, Gilead Sciences, Celgene, BeiGene, Swedish Orphan Biovitrum
Openalex Percentile: Top 43%
Lymphoma Diagnosis and Treatment
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