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Brentuximab vedotin in relapsed/refractory Hodgkin lymphoma. The Hellenic experience.
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; Anargyrou, Konstantinos; Repousis, Panagiotis; Hatzimichael, Eleutheria; Bousiou, Zoi; Poulakidas, Elias; Grentzelias, Dimitrios; Harhalakis, Nikolaos; Pangalis, Gerassimos A; Anagnostopoulos, Achilles; Tsirigotis, Panagiotis.
Afiliación
  • Angelopoulou MK; Department of Hematology, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Vassilakopoulos TP; Department of Hematology, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Batsis I; Hematology and Bone Marrow Transplantation Department, General Hospital of Thessaloniki Papanikolaou, Thessaloniki, Greece.
  • Sakellari I; Hematology and Bone Marrow Transplantation Department, General Hospital of Thessaloniki Papanikolaou, Thessaloniki, Greece.
  • Gkirkas K; 2nd Department of Internal Medicine, Faculty of Medicine, ATTIKON General University Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
  • Pappa V; 2nd Department of Internal Medicine, Faculty of Medicine, ATTIKON General University Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
  • Giannoulia P; Department of Hematology, Evaggelismos General Hospital, Athens, Greece.
  • Apostolidis I; Department of Hematology, Evaggelismos General Hospital, Athens, Greece.
  • Apostolopoulos C; Third Department of Medicine, "Sotiria" General Hospital of Thoracic Diseases, Hematology Unit, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
  • Roussou P; Third Department of Medicine, "Sotiria" General Hospital of Thoracic Diseases, Hematology Unit, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
  • Panayiotidis P; 1st Department of Propedeutic Internal Medicine, Laikon General Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
  • Dimou M; 1st Department of Propedeutic Internal Medicine, Laikon General Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
  • Kyrtsonis MC; 1st Department of Propedeutic Internal Medicine, Laikon General Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
  • Palassopoulou M; Department of Hematology, Larissa University Hospital, University of Thessalia, Larissa, Greece.
  • Vassilopoulos G; Department of Hematology, Larissa University Hospital, University of Thessalia, Larissa, Greece.
  • Moschogiannis M; Department of Hematology, Athens Medical Center, Athens, Greece.
  • Kalpadakis C; Department of Hematology, Heraklion University Hospital, University of Crete, Heraklion, Greece.
  • Margaritis D; Department of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
  • Spyridonidis A; Bone Marrow Transplantation Unit, University of Patras, Patras, Greece.
  • Michalis E; Department of Clinical Hematology, "G.Gennimatas" Athens General Hospital, Athens, Greece.
  • Anargyrou K; Department of Hematology, Air Force Hospital, Athens, Greece.
  • Repousis P; Department of Hematology, Metaxa Hospital, Pireaus, Greece.
  • Hatzimichael E; Department of Hematology, Ioannina University Hospital, University of Ioannina, Ioannina, Greece.
  • Bousiou Z; Hematology and Bone Marrow Transplantation Department, General Hospital of Thessaloniki Papanikolaou, Thessaloniki, Greece.
  • Poulakidas E; Department of Hematology, 401 Military Hospital of Athens, Athens, Greece.
  • Grentzelias D; Hygeia General Hospital, Athens, Greece.
  • Harhalakis N; Department of Hematology, Evaggelismos General Hospital, Athens, Greece.
  • Pangalis GA; Department of Hematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece.
  • Anagnostopoulos A; Hematology and Bone Marrow Transplantation Department, General Hospital of Thessaloniki Papanikolaou, Thessaloniki, Greece.
  • Tsirigotis P; 2nd Department of Internal Medicine, Faculty of Medicine, ATTIKON General University Hospital, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
Hematol Oncol ; 36(1): 174-181, 2018 Feb.
Article en En | MEDLINE | ID: mdl-28219112
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin / Inmunoconjugados Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Hematol Oncol Año: 2018 Tipo del documento: Article País de afiliación: Grecia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin / Inmunoconjugados Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Hematol Oncol Año: 2018 Tipo del documento: Article País de afiliación: Grecia