Treatment of Relapsed and Refractory Hodgkin Lymphoma – Recommendations of the Czech Hodgkin Lymphoma Study Group

Česká verze

Authors: H. Mociková ¹; J. Marková ¹; Ľ. Gahérová ¹; Z. Král ²; A. Sýkorová ³; D. Belada ³; V. Procházka ⁴ ; L. Martinková ⁵; T. Papajík ⁴; T. Kozák ¹
Authors place of work: Interní hematologická klinika 3. LF UK a FN Královské Vinohrady, Praha ¹; Interní hematologická a onkologická klinika LF MU a FN Brno ²; IV. interní hematologická klinika LF UK a FN Hradec Králové ³; Hematoonkologická klinika LF UP a FN Olomouc ⁴; Klinika hematoonkologie LF OU a FN Ostrava ⁵
Published in the journal: Klin Onkol 2016; 29(5): 342-346
Category: Přehledy
doi: https://doi.org/http://dx.doi.org/10.14735/amko2016342

Summary

High-dose chemotherapy with autologous stem cell transplantation remains the current standard of treatment for young patients with Hodgkin lymphoma in first relapse or in those who are refractory to first-line treatment. The most important prognostic factors in relapses are clinical stage IV, poor performance status, bulky mass, and less than partial remission after salvage chemotherapy. Standard salvage chemotherapy in relapse before autologous transplantation has not been defined; however, DHAP and ICE are most frequently used in this setting. A standard conditioning regimen before autologous transplantation is BEAM. Tandem autologous transplantation has been investigated in high-risk patients. Brentuximab vedotin is recommended as a consolidation treatment in patients with a high risk of relapse after autologous transplantation. Brentuximab vedotin is the standard of treatment for relapse after autologous transplantation, and subsequent allogeneic stem cell transplantation should be considered in young patients. Bretuximab vedotin in combination with bendamustine, nivolumab, and pembrolizumab, and combinations thereof with other drugs, were investigated in clinical trials in relapsed or refractory patients with Hodgkin lymphoma.

Key words:
Hodgkin lymphoma – autologous stem cell transplantation – brentuximab vedotin – nivolumab

This work was supported by grant awarded by AZV 16-29857, Ministry of Health in Czech Republic, Research project P 27/2012 awarded by Charles University in Prague, 3rd Faculty of Medicine, Prague.

The authors declare they have no potential confl icts of interest concerning drugs, products, or services used in the study.

The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.

Submitted:
7. 6. 2016

Accepted:
24. 8. 2016

Zdroje

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