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Outcome of patients with Fanconi anemia developing myelodysplasia and acute leukemia who received allogeneic hematopoietic stem cell transplantation: A retrospective analysis on behalf of EBMT group.
Giardino, Stefano; de Latour, Regis P; Aljurf, Mahmoud; Eikema, Dirk-Jan; Bosman, Paul; Bertrand, Yves; Tbakhi, Abdelghani; Holter, Wolfgang; Bornhäuser, Martin; Rössig, Claudia; Burkhardt, Birgit; Zecca, Marco; Afanasyev, Boris; Michel, Gerard; Ganser, Arnold; Alseraihy, Amal; Ayas, Mouhab; Uckan-Cetinkaya, Duygu; Bruno, Benedicte; Patrick, Katharine; Bader, Peter; Itälä-Remes, Maija; Rocha, Vanderson; Jubert, Charlotte; Diaz, Miguel A; Shaw, Peter J; Junior, Luiz G D; Locatelli, Franco; Kröger, Nicolaus; Faraci, Maura; Pierri, Filomena; Lanino, Edoardo; Miano, Maurizio; Risitano, Antonio; Robin, Marie; Dufour, Carlo.
Afiliación
  • Giardino S; Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.
  • de Latour RP; French reference center for aplastic anemia and PNH;Saint-Louis Hospital, Université de Paris, Paris, France.
  • Aljurf M; King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Eikema DJ; EBMT Statistical Unit, Leiden, The Netherlands.
  • Bosman P; EBMT Data Office, Leiden, The Netherlands.
  • Bertrand Y; IHOP, Lyon, France.
  • Tbakhi A; King Hussein Cancer Centre, Amman, Jordan.
  • Holter W; St. Anna Kinderspital, Vienna, Austria.
  • Bornhäuser M; UniversitätsKlinikum Dresden, TU, Dresden, Germany.
  • Rössig C; Pediatric Hematology and Oncology, University Children´s Hospital Muenster, Muenster, Germany.
  • Burkhardt B; Pediatric Hematology and Oncology, University Children´s Hospital Muenster, Muenster, Germany.
  • Zecca M; Fondazione IRCSS Policlinico San Matteo, Pavia, Italy.
  • Afanasyev B; First State Medical University, St. Petersburg, Russia.
  • Michel G; Hopital d'Enfants de la Timone, Marseille, France.
  • Ganser A; Hannover Medical School, Hannover, Germany.
  • Alseraihy A; King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Ayas M; King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Uckan-Cetinkaya D; Hacettepe University Children's Hospital, Ankara, Turkey.
  • Bruno B; CHU Lille, Service d'hématologie Pédiatrique, Lille, France.
  • Patrick K; Sheffield Childrens NHS Foundation Trust, Sheffield, UK.
  • Bader P; Immunologie und Intensivmedizin, Klinikum der Johann-Wolfgang Goethe Universität, Klinik für Kinder-und Jugendmedizin, Schwerpunkt Stammzelltransplantation, Frankfurt am Main, Germany.
  • Itälä-Remes M; HUCH Comprehensive Cancer Center, Helsinki, Finland.
  • Rocha V; Hospital Sirio-Libanes, Brazil.
  • Jubert C; Bordeaux Groupe Hospitalier Pellegrin-Enfants, Bordeaux, France.
  • Diaz MA; Hospital Infantil Universitario "Niño Jesus", Madrid, Spain.
  • Shaw PJ; The Children's Hospital at Westmead, Sydney, Australia.
  • Junior LGD; Ribeirao Preto Medical School, Sao Paulo, Brazil.
  • Locatelli F; IRCSS OspedalePediatrico Bambino Gesù, Sapienza, University of Rome, Rome, Italy.
  • Kröger N; University Hospital Eppendorf, Hamburg, Germany.
  • Faraci M; Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.
  • Pierri F; Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.
  • Lanino E; Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.
  • Miano M; UOC Ematologia, Istituto Giannina Gaslini, Genoa, Italy.
  • Risitano A; Università Federico II, Naples, Italy.
  • Robin M; French reference center for aplastic anemia and PNH;Saint-Louis Hospital, Université de Paris, Paris, France.
  • Dufour C; UOC Ematologia, Istituto Giannina Gaslini, Genoa, Italy.
Am J Hematol ; 95(7): 809-816, 2020 07.
Article en En | MEDLINE | ID: mdl-32267023
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is curative for bone marrow failure in patients with Fanconi anemia (FA), but the presence of a malignant transformation is associated with a poor prognosis and the management of these patients is still challenging. We analyzed outcome of 74 FA patients with a diagnosis of myelodysplastic syndrome (n = 35), acute leukemia (n = 35) or with cytogenetic abnormalities (n = 4), who underwent allo-HSCT from 1999 to 2016 in EBMT network. Type of diagnosis, pre-HSCT cytoreductive therapies and related toxicities, disease status pre-HSCT, donor type, and conditioning regimen were considered as main variables potentially influencing outcome. The 5-year OS and EFS were 42% (30-53%) and 39% (27-51%), respectively. Patients transplanted in CR showed better OS compared with those transplanted in presence of an active malignant disease (OS:71%[48-95] vs 37% [24-50],P = .04), while none of the other variables considered had an impact. Twenty-two patients received pre-HSCT cytoreduction and 9/22 showed a grade 3-4 toxicity, without any lethal event or negative influence on survival after HSCT(OS:toxicity pre-HSCT 48% [20-75%] vs no-toxicity 51% [25-78%],P = .98). The cumulative incidence of day-100 grade II-IV a-GvHD and of 5-year c-GvHD were 38% (26-50%) and 40% (28-52%). Non-relapse-related mortality and incidence of relapse at 5-years were 40% (29-52%) and 21% (11-30%) respectively, without any significant impact of the tested variables. Causes of death were transplant-related events in most patients (34 out of the 42 deaths, 81%). This analysis confirms the poor outcome of transformed FA patients and identifies the importance of achieving CR pre-HSCT, suggesting that, in a newly diagnosed transformed FA patient, a cytoreductive approach pre-HSCT should be considered if a donor have been secured.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Leucemia / Trasplante de Células Madre Hematopoyéticas / Anemia de Fanconi Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Hematol Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Leucemia / Trasplante de Células Madre Hematopoyéticas / Anemia de Fanconi Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Hematol Año: 2020 Tipo del documento: Article