Salvage Therapy for Hodgkin's Lymphoma: A Review of Current Regimens and Outcomes
- PMID: 33149713
- PMCID: PMC7603406
- DOI: 10.2147/JBM.S250581
Salvage Therapy for Hodgkin's Lymphoma: A Review of Current Regimens and Outcomes
Abstract
Relapse/refractory Hodgkin lymphoma patients are still a clinical concern. Indeed, despite more effective first-line chemotherapy regimens and better stratification of unresponsive patients by clinical factors and use of early PET, roughly one-third of such patients need salvage chemotherapy and consolidation with high-dose chemotherapy. In this paper, the authors review the different salvage treatments, with special emphasis on newer combinations with brentuximab vedotin or check point inhibitors. The overall response rate is constantly increasing, with a complete remission rate approaching 80%. Functional response evaluation by PET imaging is a strong predictive factor of longer survival, and more sophisticated tools, such as detection of circulating tumour DNA, are emerging to refine the disease-status assessment after treatment. Consolidation by high-dose chemotherapy is still considered the standard of care in chemosensitive patients, leading to a high fraction of patients towards long-term disease control. Maintenance therapy with BV is now approved, reducing disease relapse/progression. An increasing number of Hodgkin lymphoma patients will be cured after first- and second-line therapy, and long-term toxicity needs to be continuously assessed and avoided.
Keywords: Hodgkin lymphoma; brentuximab vedotin; checkpoint inhibitors; high-dose chemotherapy; refractory/relapsed disease.
© 2020 Castagna et al.
Conflict of interest statement
Armando Santoro reports advisory board for BMS, SERVIER, GILEAD, PFIZER, EISAI, BAYER, and MSD, consultancy for ARQULE and SANOFI, speaker’s bureau for TAKEDA, BMS, ROCHE, ABB-VIE, AMGEN, CELGENE, SERVIER, GILEAD, ASTRAZENECA, PFIZER, ARQULE, LILLY, SANDOZ, EISAI, NOVARTIS, BAYER, and MSD, during the conduct of the study. C. Carlo-Stella has received research support from ADC Therapeutics and Rhizen Pharmaceuticals; has served as consultant or advisor for Servier, Novartis, Genenta Science srl, ADC Therapeutics, Roche, Sanofi, Karyopharm; and has received honoraria for speaker engagements from Bristol-Myers Squibb, Merck Sharp & Dohme, Janssen Oncology, Astra-ZenecaLuca Castagna. The authors report no other potential conflicts of interest in this work.
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