TY - JOUR TI - Brentuximab vedotin in relapsed/refractory Hodgkin lymphoma. The Hellenic experience AU - Angelopoulou, M.K. AU - Vassilakopoulos, T.P. AU - Batsis, I. AU - Sakellari, I. AU - Gkirkas, K. AU - Pappa, V. AU - Giannoulia, P. AU - Apostolidis, I. AU - Apostolopoulos, C. AU - Roussou, P. AU - Panayiotidis, P. AU - Dimou, M. AU - Kyrtsonis, M.-C. AU - Palassopoulou, M. AU - Vassilopoulos, G. AU - Moschogiannis, M. AU - Kalpadakis, C. AU - Margaritis, D. AU - Spyridonidis, A. AU - Michalis, E. AU - Anargyrou, K. AU - Repousis, P. AU - Hatzimichael, E. AU - Bousiou, Z. AU - Poulakidas, E. AU - Grentzelias, D. AU - Harhalakis, N. AU - Pangalis, G.A. AU - Anagnostopoulos, A. AU - Tsirigotis, P. JO - Journal of Hematology & Oncology PY - 2018 VL - 36 TODO - 1 SP - 174-181 PB - John Wiley and Sons Ltd SN - 1756-8722 TODO - 10.1002/hon.2383 TODO - brentuximab vedotin; antibody conjugate; brentuximab vedotin, adult; allogeneic stem cell transplantation; Article; autologous stem cell transplantation; cancer chemotherapy; cancer radiotherapy; cancer recurrence; cancer survival; chemosensitivity; disease control; disease exacerbation; female; follow up; Hodgkin disease; human; major clinical study; male; overall survival; patient history of chemotherapy; priority journal; progression free survival; retrospective study; salvage therapy; treatment failure; clinical trial; Hodgkin disease; mortality; multicenter study; pathology; prognosis; survival analysis; treatment outcome, Adult; Female; Hodgkin Disease; Humans; Immunoconjugates; Male; Prognosis; Retrospective Studies; Survival Analysis; Treatment Outcome TODO - This retrospective study aimed to describe the Hellenic experience on the use of brentuximab vedotin (BV) in relapsed/refractory (R/R) Hodgkin lymphoma (HL) given within its indication. From June 2011 to April 2015, ninety-five patients with R/R HL, who received BV in 20 centers from Greece, were analyzed. Their median age was 33 years, and 62% were males. Sixty-seven patients received BV after autologous stem cell transplantation failure, whereas 28 patients were treated with BV without a prior autologous stem cell transplantation, due to advanced age/comorbidities or chemorefractory disease. The median number of prior treatments was 4 and 44% of the patients were refractory to their most recent therapy. The median number of BV cycles was 8 (range, 2-16), and the median time to best response was the fourth cycle. Fifty-seven patients achieved an objective response: twenty-two (23%), a complete response (CR), and 35 patients (37%), a partial, for an overall response rate of 60%. Twelve patients (13%) had stable disease, and the remaining twenty-six (27%) had progressive disease as their best response. At a median follow-up of 11.5 months, median progression-free survival and overall survival were 8 and 26.5 months, respectively. Multivariate analysis showed that chemosensitivity to treatment administered before BV was associated with a significantly increased probability of achieving response to BV (P =.005). Bulky disease (P =.01) and response to BV (P <.001) were significant for progression-free survival, while refractoriness to most recent treatment (P =.04), bulky disease (P =.005), and B-symptoms (P =.001) were unfavorable factors for overall survival. Among the 22 CRs, 5 remain in CR with no further treatment after BV at a median follow-up of 13 months. In conclusion, our data indicate that BV is an effective treatment for R/R HL patients even outside clinical trials. Whether BV can cure a fraction of patients remains to be seen. © 2017 The Authors Hematological Oncology Published by John Wiley & Sons Ltd ER -