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Idelalisib treatment prior to allogeneic stem cell transplantation for patients with chronic lymphocytic leukemia: a report from the EBMT chronic malignancies working party.
Schetelig, Johannes; Chevallier, Patrice; van Gelder, Michel; Hoek, Jennifer; Hermine, Olivier; Chakraverty, Ronjon; Browne, Paul; Milpied, Noel; Malagola, Michele; Socié, Gerard; Delgado, Julio; Deconinck, Eric; Damaj, Ghandi; Maury, Sebastian; Beelen, Dietrich; Quoc, Stéphanie Nguyen; Shankara, Paneesha; Brecht, Arne; Mayer, Jiri; Hunault-Berger, Mathilde; Bittenbring, Jörg; Thieblemont, Catherine; Lepretre, Stéphane; Baldauf, Henning; de Wreede, Liesbeth C; Tournilhac, Olivier; Yakoub-Agha, Ibrahim; Kröger, Nicolaus; Dreger, Peter.
Afiliação
  • Schetelig J; Medical Clinic I, University Hospital, Dresden, Germany. johannes.schetelig@uniklinikum-dresden.de.
  • Chevallier P; DKMS, Dresden, Germany. johannes.schetelig@uniklinikum-dresden.de.
  • van Gelder M; CHU Nantes, Nantes, France.
  • Hoek J; University Hospital Maastricht, Maastricht, The Netherlands.
  • Hermine O; EBMT Data Office, Leiden, The Netherlands.
  • Chakraverty R; Department of Hematology, Necker Hospital and INSERM U1163 Imagine Institute, University of Paris, Paris, France.
  • Browne P; Cancer Institute and Institute of Immunity and Transplantation, University College London Hospital, London, UK.
  • Milpied N; Hope Directorate, Dublin, Ireland.
  • Malagola M; CHU Bordeaux, Pessac, France.
  • Socié G; Bone Marrow Transplant Unit, ASST-Spedali Civili di Brescia, University of Brescia, Brescia, Italy.
  • Delgado J; Hopital St. Louis, Paris, France.
  • Deconinck E; Hospital Clinic, Barcelona, Spain.
  • Damaj G; Hopital Jean Minjoz, Besancon, France.
  • Maury S; Centre Hospitalier-Universitaire, Institut d'Hématologie, Normandie University, Caen, France.
  • Beelen D; Service d'Hématologie Clinique et de Thérapie Cellulaire Creteil, CHU Henri Mondor, Créteil, France.
  • Quoc SN; University Hospital, Essen, Germany.
  • Shankara P; Hopital la Pitié-Salpêtrière, Universite Paris IV, Paris, France.
  • Brecht A; Birmingham Heartlands Hospital, Birmingham, UK.
  • Mayer J; Helios Dr. Horst Schmidt Kliniken, Wiesbaden, Germany.
  • Hunault-Berger M; University Hospital Brno, Brno, Czech Republic.
  • Bittenbring J; Maladies du Sang, CHU Angers, Angers, France.
  • Thieblemont C; University of Saarland, Homburg, Saar, Germany.
  • Lepretre S; Hôpital St. Louis, Paris, France.
  • Baldauf H; Inserm U1245 and Department of Hematology, Centre Henri Becquerel, Normandie University, Rouen, France.
  • de Wreede LC; DKMS, Dresden, Germany.
  • Tournilhac O; Department of Medical Statistics & Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Yakoub-Agha I; Service Therapie Cellulaire & Hematologie Cliniquer, Centre Hospitalier Universitaire, Clermont Ferrand, France.
  • Kröger N; Centre Hospitalier Universitaire de Lille, LIRIC, INSERM U995, Université de Lille, Lille, France.
  • Dreger P; University Hospital Eppendorf, Hamburg, Germany.
Bone Marrow Transplant ; 56(3): 605-613, 2021 03.
Article em En | MEDLINE | ID: mdl-33004942
ABSTRACT
No studies have been reported so far on bridging treatment with idelalisib for patients with chronic lymphocytic leukemia (CLL) prior to allogeneic hematopoietic cell transplantation (alloHCT). To study potential carry-over effects of idelalisib and to assess the impact of pathway-inhibitor (PI) failure we performed a retrospective EBMT registry-based study. Patients with CLL who had a history of idelalisib treatment and received a first alloHCT between 2015 and 2017 were eligible. Data on 72 patients (median age 58 years) were analyzed. Forty percent of patients had TP53mut/del CLL and 64% had failed on at least one PI. No primary graft failure occurred. Cumulative incidences of acute GVHD °II-IV and chronic GVHD were 51% and 39%, respectively. Estimates for 2-year overall survival (OS), progression-free survival (PFS), and cumulative incidences of relapse/progression (CIR) and non-relapse mortality NRM were 59%, 44%, 25%, and 31%. In univariate analysis, drug sensitivity was a strong risk factor. For patients who had failed neither PI treatment nor chemoimmunotherapy (CIT) the corresponding 2-year estimates were 73%, 65%, 15%, and 20%, respectively. In conclusion, idelalisib may be considered as an option for bridging therapy prior to alloHCT. Owing to the high risk for acute GVHD intensified clinical monitoring is warranted.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article