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Brentuximab vedotin and bendamustine: an effective salvage therapy for relapsed or refractory Hodgkin lymphoma patients.

Authors :
Uncu Ulu B
Dal MS
Yönal Hindilerden İ
Akay OM
Mehtap Ö
Büyükkurt N
Hindilerden F
Güneş AK
Yiğenoğlu TN
Başcı S
Kızıl Çakar M
Yanardağ Açık D
Korkmaz S
Ulaş T
Özet G
Ferhanoğlu B
Nalçacı M
Altuntaş F
Source :
Journal of chemotherapy (Florence, Italy) [J Chemother] 2022 May; Vol. 34 (3), pp. 190-198. Date of Electronic Publication: 2021 Sep 13.
Publication Year :
2022

Abstract

The prognosis is poor for relapsed or refractory (R/R) classical Hodgkin Lymphoma (cHL) patients. The brentuximab vedotin (Bv) and bendamustine (B) combination has been used as a preferable salvage regimen in R/R cHL patient trials. We retrospectively evaluated response rates, toxicities, and the survival in R/R cHL patients treated with the BvB combination. In a multi-centre real-life study, 61 R/R HL patients received intravenous doses of 1.8 mg/kg Bv on the first day plus 90 mg/m <superscript>2</superscript> B on the first and second days of a 21-day cycle as a second-line or beyond-salvage regimen. Patients' median age at BvB initiation was 33 (range: 18-76 years). BvB was given as median third-line treatment for a median of four cycles (range: 2-11). The overall and complete response rates were 82% and 68.9%, respectively. After BvB initiation, the median follow-up was 14 months, and one- and two-year overall survival rates were 85% and 72%, respectively. Grade 3/4 toxicities included neutropenia (24.6%), lymphopenia (40%), thrombocytopenia (13%), anaemia (13%), infusion reactions (8.2%), neuropathy (6.5%), and others. The BvB combination could be given as salvage regimen aiming a bridge to autologous stem cell transplant (ASCT), in patients relapse after ASCT or to transplant-ineligible patients with manageable toxicity profiles.

Details

Language :
English
ISSN :
1973-9478
Volume :
34
Issue :
3
Database :
MEDLINE
Journal :
Journal of chemotherapy (Florence, Italy)
Publication Type :
Academic Journal
Accession number :
34514960
Full Text :
https://doi.org/10.1080/1120009X.2021.1976912