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A phase II trial of bendamustine, carboplatin, and dexamethasone for refractory or relapsed peripheral T-cell lymphoma (BENCART trial)

Authors
Park, Byeong-BaeKim, Won SeogSuh, CheolwonHong, Jung YongYang, Deok-HwanLee, Won SikDo, Young RokKoh, Young IlWon, Jong-HoKim, Min KyoungJo, Jae-CheolHyun, Shin YoungKim, Jeong-AOh, Young HaLee, Seung-Sook
Issue Date
Nov-2019
Publisher
TAYLOR & FRANCIS LTD
Keywords
Lymphoma and Hodgkin disease; neoplasia; salvage therapy; bendamustine
Citation
LEUKEMIA & LYMPHOMA, v.60, no.13, pp.3251 - 3257
Indexed
SCIE
SCOPUS
Journal Title
LEUKEMIA & LYMPHOMA
Volume
60
Number
13
Start Page
3251
End Page
3257
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/11703
DOI
10.1080/10428194.2019.1622100
ISSN
1042-8194
Abstract
This trial was designed to investigate the efficacy and toxicity of bendamustine, carboplatin, and dexamethasone (BCD) for relapsed or refractory peripheral T-cell lymphomas (PTCLs), which would be expected to exhibit more promising clinical outcomes compared with bendamustine therapy alone. After treatments with BCD, eight patients exhibited a complete response (CR; 29%) and seven exhibited a partial response (PR; 25%). The overall response rate (ORR) was 54%. Five patients proceeded to ASCT and three patients finally achieved CR. The median progression-free survival (PFS) was 4.4 months (2.8-6.0, 95% CI). For a total of 85 cycles of BCD, grade 3 or 4 neutropenia, thrombocytopenia, and anemia occurred in 17.6, 38.8, and 16.5% of cycles, respectively. Only one patient experienced febrile neutropenia. BCD was a considerable salvage regimen for relapsed or refractory PTCLs with acceptable toxicity; AITL or ASCT eligible patients were more effective to BCD. ClinicalTrials.gov Identifier: NCT02424045
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