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Long-term results of brentuximab vedotin in relapsed and refractory Hodgkin lymphoma: multi-center real-life experience
Authors:Murat &#  zbalak,Ay&#  e Saliho&#  lu,Teoman Soysal,&#  hsan Karado&#  an,Semra Payda&#  ,Evren &#  zdemir,Birol Y&#  ld&#  z,Nuri Karadurmu&#  ,Leylag&#  l Kaynar,M&#  nci Yagci,Vildan &#  zkocaman,Pervin Top&#  uo&#  lu,Muhit &#  zcan,Elif Birta&#  ,Hakan G&#  ker,Burhan Ferhanoglu
Affiliation:1.Division of Hematology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey;2.Division of Hematology, Istanbul University Cerrahpa?a, Istanbul, Turkey;3.Division of Hematology, Antalya Medstar Hospital, Antalya, Turkey;4.Department of Internal Medicine, Division of Medical Oncology, Cukurova University, Adana, Turkey;5.Department of Oncology, Medicana International Hospital, Ankara, Turkey;6.Department of Internal Medicine, Division of Medical Oncology, Gulhane Research and Training Hospital, Ankara, Turkey;7.Division of Hematology, Erciyes University, Kayseri, Turkey;8.Division of Hematology, Gazi University, Ankara, Turkey;9.Division of Hematology, Uludag University, Bursa, Turkey;10.Division of Hematology, Ankara University, Ankara, Turkey;11.Division of Hematology, Anadolu Medical Center, Kocaeli, Turkey;12.Division of Hematology, Hacettepe University, Ankara, Turkey;13.Department of Hematology, Koc University School of Medicine and V.K.V. American Hospital, Istanbul, Turkey
Abstract:Classical Hodgkin lymphoma (cHL) is considered a curable disease; however, approximately one-third of responders experience disease relapse following first-line therapy. Several studies have shown the efficacy of brentuximab vedotin (BV) in patients with relapsed/refractory HL. We present a retrospective analysis of 58 patients with relapsed/refractory HL treated with BV in a named patient program from 11 centers. The median follow-up duration was 20 (range, 4–84) months. The best overall response rate was 64% (complete response [CR], 31%; partial response [PR], 33%). The 5-year progression-free survival (PFS) and overall survival (OS) rates were 12% (95% confidence interval [CI], 0.05–0.22) and 26% (95% CI, 0.16–0.38), respectively. Among patients who achieved CR, the estimated 5-year PFS and OS rates were 32% (95% CI, 0.13–0.54) and 60% (95% CI, 0.33–0.78), respectively. A total of 26 patients underwent subsequent stem cell transplantation. The 5-year PFS and OS rates for 10 patients who had consolidative stem cell transplantation were 28% and 30%, respectively. Twenty-seven patients required further therapy following BV. At the time of the analysis, 12 patients (21%) were alive. Five patients (9%) had long-term remission after achieving CR with BV monotherapy, with a median PFS of 76 months. Three of them (5%) did not receive any other treatment following BV and their median PFS was 75 months. Our long-term results showed that a small subset of patients with relapsed/refractory cHL may benefit from and even be cured with BV monotherapy.
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