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Prognostic value of TARC and quantitative PET parameters in relapsed or refractory Hodgkin lymphoma patients treated with brentuximab vedotin and DHAP

Julia Driessen, Marie José Kersten*, Lydia Visser, Anke van den Berg, Sanne H Tonino, Josée M Zijlstra, Pieternella J Lugtenburg, Franck Morschhauser, Martin Hutchings, Sandy Amorim, Thomas Gastinne, Marcel Nijland, Gerben J C Zwezerijnen, Ronald Boellaard, Henrica C W de Vet, Anne I J Arens, Roelf Valkema, Roberto D K Liu, Esther E E Drees, Daphne de JongWouter J Plattel, Arjan Diepstra*, HOVON Lunenburg Lymphoma Phase I/II Consortium (LLPC)

*Corresponding author for this work
20 Citations (Scopus)

Abstract

Risk-stratified treatment strategies have the potential to increase survival and lower toxicity in relapsed/refractory classical Hodgkin lymphoma (R/R cHL) patients. This study investigated the prognostic value of serum (s)TARC, vitamin D and lactate dehydrogenase (LDH), TARC immunohistochemistry and quantitative PET parameters in 65 R/R cHL patients who were treated with brentuximab vedotin (BV) and DHAP followed by autologous stem-cell transplantation (ASCT) within the Transplant BRaVE study (NCT02280993). At a median follow-up of 40 months, the 3-year progression free survival (PFS) was 77% (95% CI: 67-88%) and the overall survival was 95% (90-100%). Significant adverse prognostic markers for progression were weak/negative TARC staining of Hodgkin Reed-Sternberg cells in the baseline biopsy, and a high standard uptake value (SUV)mean or SUVpeak on the baseline PET scan. After one cycle of BV-DHAP, sTARC levels were strongly associated with the risk of progression using a cutoff of 500 pg/ml. On the pre-ASCT PET scan, SUVpeak was highly prognostic for progression post-ASCT. Vitamin D, LDH and metabolic tumor volume had low prognostic value. In conclusion, we established the prognostic impact of sTARC, TARC staining, and quantitative PET parameters for R/R cHL, allowing the use of these parameters in prospective risk-stratified clinical trials. Trial registration: NCT02280993.

Original languageEnglish
JournalLeukemia
Volume36
Issue number12
Pages (from-to)2853-2862
Number of pages10
ISSN0887-6924
DOIs
Publication statusPublished - Dec 2022

Keywords

  • Brentuximab Vedotin
  • Hodgkin Disease/diagnostic imaging
  • Humans
  • Immunoconjugates/therapeutic use
  • Neoplasm Recurrence, Local/diagnostic imaging
  • Positron-Emission Tomography
  • Prognosis
  • Prospective Studies
  • Stem Cell Transplantation
  • Vitamin D/therapeutic use

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