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Brentuximab vedotin in relapsed/refractory Hodgkin lymphoma. The Hellenic experience.

Authors :
Angelopoulou, Maria K.
Vassilakopoulos, Theodoros P.
Batsis, Ioannis
Sakellari, Ioanna
Gkirkas, Konstantinos
Pappa, Vasiliki
Giannoulia, Panagiota
Apostolidis, Ioannis
Apostolopoulos, Christos
Roussou, Paraskevi
Panayiotidis, Panayiotis
Dimou, Maria
Kyrtsonis, Marie‐Christine
Palassopoulou, Maria
Vassilopoulos, Georgios
Moschogiannis, Maria
Kalpadakis, Christina
Margaritis, Dimitrios
Spyridonidis, Alexander
Michalis, Eurydiki
Source :
Hematological Oncology; Feb2018, Vol. 36 Issue 1, p174-181, 8p
Publication Year :
2018

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02780232
Volume :
36
Issue :
1
Database :
Complementary Index
Journal :
Hematological Oncology
Publication Type :
Academic Journal
Accession number :
128133796
Full Text :
https://doi.org/10.1002/hon.2383