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Long-term results and GvHD after prophylactic and preemptive donor lymphocyte infusion after allogeneic stem cell transplantation for acute leukemia.
Schmid, Christoph; Labopin, Myriam; Schaap, Nicolaas; Veelken, Hendrik; Brecht, Arne; Stadler, Michael; Finke, Juergen; Baron, Frederic; Collin, Matthew; Bug, Gesine; Ljungman, Per; Blaise, Didier; Tischer, Johanna; Bloor, Adrian; Kulagin, Aleksander; Giebel, Sebastian; Gorin, Norbert-Claude; Esteve, Jordi; Ciceri, Fabio; Savani, Bipin; Nagler, Arnon; Mohty, Mohamad.
Afiliación
  • Schmid C; Department of Hematology and Oncology, Augsburg University Hospital and Medical Faculty, Augsburg, Germany. Christoph.Schmid@uk-augsburg.de.
  • Labopin M; EBMT Study Office, Saint Antoine Hospital, Paris, France.
  • Schaap N; INSERM UMR 938, Sorbonne University, Paris, France.
  • Veelken H; Radboud University Medical Centre Nijmegen, Nijmegen, The Netherlands.
  • Brecht A; Department of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
  • Stadler M; Helios Dr. Horst Schmidt Kliniken, Wiesbaden, Germany.
  • Finke J; Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
  • Baron F; Department of Hematology and Medical Oncology, University of Freiburg, Freiburg, Germany.
  • Collin M; Department of Medicine, Division of Hematology, University of Liège, Belgium, Liege.
  • Bug G; Bone Marrow Transplant Unit, Northern Centre for Bone Marrow Transplantation, Newcastle-upon-Tyne, UK.
  • Ljungman P; Department of Medicine 2, Goethe University Frankfurt, Frankfurt am Main, Germany.
  • Blaise D; Department of Cellular Therapy and Allogeneic Stem Cell Transplantation, Karolinska University Hospital Huddinge, Stockholm, Sweden.
  • Tischer J; Programme de Transplantation & Therapie Cellulaire-Centre de Recherche en Cancérologie de Marseille-Institut Paoli Calmettes, Marseille, France.
  • Bloor A; Department of Medicine 3, Hematology and Oncology, Ludwig-Maximilian-University, Munich, Germany.
  • Kulagin A; Stem Cell Transplantation Unit, The Christie NHS Foundation Trust, Manchester, UK.
  • Giebel S; RM Gorbacheva Research Institute, Pavlov University, St. Petersburg, Russia.
  • Gorin NC; Department of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie Institute - Oncology Center, Gliwice Branch, Gliwice, Poland.
  • Esteve J; Faculté de Médicine Saint-Antoine and EBM study office, Saint Antoine Hospital, Paris, France.
  • Ciceri F; Hospital Clinic Barcelona, Institute of Hematology and Oncology, Barcelona, Spain.
  • Savani B; Hematology and Bone Marrow Transplantation Unit, San Raffaele Scientific Institute, Milano, Italy.
  • Nagler A; Vanderbilt University Medical Center, Nashville, TN, USA.
  • Mohty M; BMT and Cord Blood Bank, Chaim Sheba Medical Center, Tel Aviv University, Tel-Hashomer, Israel.
Bone Marrow Transplant ; 57(2): 215-223, 2022 02.
Article en En | MEDLINE | ID: mdl-34750562
We report on 318 patients with acute leukemia, receiving donor lymphocyte infusion (DLI) in complete hematologic remission (CHR) after allogeneic stem cell transplantation (alloSCT). DLI were applied preemptively (preDLI) for minimal residual disease (MRD, n = 23) or mixed chimerism (MC, n = 169), or as prophylaxis in high-risk patients with complete chimerism and molecular remission (proDLI, n = 126). Median interval from alloSCT to DLI1 was 176 days, median follow-up was 7.0 years. Five-year cumulative relapse incidence (CRI), non-relapse mortality (NRM), leukemia-free and overall survival (LFS/OS) of the entire cohort were 29.1%, 12.7%, 58.2%, and 64.3%. Cumulative incidences of acute graft-versus-host disease (aGvHD) grade II-IV°/chronic GvHD were 11.9%/31%. Nineteen patients (6%) died from DLI-induced GvHD. Age ≥60 years (p = 0.046), advanced stage at transplantation (p = 0.003), shorter interval from transplantation (p = 0.018), and prior aGvHD ≥II° (p = 0.036) were risk factors for DLI-induced GvHD. GvHD did not influence CRI, but was associated with NRM and lower LFS/OS. Efficacy of preDLI was demonstrated by decreasing MRD/increasing blood counts in 71%, and increasing chimerism in 70%. Five-year OS after preDLI for MRD/MC was 51%/68% among responders, and 37% among non-responders. The study describes response and outcome of DLI in CHR and helps to identify candidates without increased risk of severe GvHD.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Middle aged Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Middle aged Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido