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

نویسندگان

  • Maria K. Angelopoulou
  • Theodoros P. Vassilakopoulos
  • Ioannis Batsis
  • Ioanna Sakellari
  • Konstantinos Gkirkas
  • Vasiliki Pappa
  • Panagiota Giannoulia
  • Ioannis Apostolidis
  • Christos Apostolopoulos
  • Paraskevi Roussou
  • Panayiotis Panayiotidis
  • Maria Dimou
  • Marie‐Christine Kyrtsonis
  • Maria Palassopoulou
  • Georgios Vassilopoulos
  • Maria Moschogiannis
  • Christina Kalpadakis
  • Dimitrios Margaritis
  • Alexander Spyridonidis
  • Eurydiki Michalis
  • Konstantinos Anargyrou
  • Panagiotis Repousis
  • Eleutheria Hatzimichael
  • Zoi Bousiou
  • Elias Poulakidas
  • Dimitrios Grentzelias
  • Nikolaos Harhalakis
  • Gerassimos A. Pangalis
  • Achilles Anagnostopoulos
  • Panagiotis Tsirigotis
چکیده

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.

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عنوان ژورنال:

دوره 36  شماره 

صفحات  -

تاریخ انتشار 2018