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.


Journal

American journal of hematology
ISSN: 1096-8652
Titre abrégé: Am J Hematol
Pays: United States
ID NLM: 7610369

Informations de publication

Date de publication:
07 2020
Historique:
received: 23 03 2020
revised: 29 03 2020
accepted: 30 03 2020
pubmed: 9 4 2020
medline: 18 8 2020
entrez: 9 4 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32267023
doi: 10.1002/ajh.25810
doi:

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

809-816

Informations de copyright

© 2020 Wiley Periodicals, Inc.

Références

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Auteurs

Stefano Giardino (S)

Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.

Regis P de Latour (RP)

French reference center for aplastic anemia and PNH;Saint-Louis Hospital, Université de Paris, Paris, France.

Mahmoud Aljurf (M)

King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.

Dirk-Jan Eikema (DJ)

EBMT Statistical Unit, Leiden, The Netherlands.

Paul Bosman (P)

EBMT Data Office, Leiden, The Netherlands.

Yves Bertrand (Y)

IHOP, Lyon, France.

Abdelghani Tbakhi (A)

King Hussein Cancer Centre, Amman, Jordan.

Wolfgang Holter (W)

St. Anna Kinderspital, Vienna, Austria.

Martin Bornhäuser (M)

UniversitätsKlinikum Dresden, TU, Dresden, Germany.

Claudia Rössig (C)

Pediatric Hematology and Oncology, University Children´s Hospital Muenster, Muenster, Germany.

Birgit Burkhardt (B)

Pediatric Hematology and Oncology, University Children´s Hospital Muenster, Muenster, Germany.

Marco Zecca (M)

Fondazione IRCSS Policlinico San Matteo, Pavia, Italy.

Boris Afanasyev (B)

First State Medical University, St. Petersburg, Russia.

Gerard Michel (G)

Hopital d'Enfants de la Timone, Marseille, France.

Arnold Ganser (A)

Hannover Medical School, Hannover, Germany.

Amal Alseraihy (A)

King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.

Mouhab Ayas (M)

King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.

Duygu Uckan-Cetinkaya (D)

Hacettepe University Children's Hospital, Ankara, Turkey.

Benedicte Bruno (B)

CHU Lille, Service d'hématologie Pédiatrique, Lille, France.

Katharine Patrick (K)

Sheffield Childrens NHS Foundation Trust, Sheffield, UK.

Peter Bader (P)

Immunologie und Intensivmedizin, Klinikum der Johann-Wolfgang Goethe Universität, Klinik für Kinder-und Jugendmedizin, Schwerpunkt Stammzelltransplantation, Frankfurt am Main, Germany.

Maija Itälä-Remes (M)

HUCH Comprehensive Cancer Center, Helsinki, Finland.

Vanderson Rocha (V)

Hospital Sirio-Libanes, Brazil.

Charlotte Jubert (C)

Bordeaux Groupe Hospitalier Pellegrin-Enfants, Bordeaux, France.

Miguel A Diaz (MA)

Hospital Infantil Universitario "Niño Jesus", Madrid, Spain.

Peter J Shaw (PJ)

The Children's Hospital at Westmead, Sydney, Australia.

Luiz G D Junior (LGD)

Ribeirao Preto Medical School, Sao Paulo, Brazil.

Franco Locatelli (F)

IRCSS OspedalePediatrico Bambino Gesù, Sapienza, University of Rome, Rome, Italy.

Nicolaus Kröger (N)

University Hospital Eppendorf, Hamburg, Germany.

Maura Faraci (M)

Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.

Filomena Pierri (F)

Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.

Edoardo Lanino (E)

Hematopoietic stem cell transplantation Unit, Istituto Giannina Gaslini, Genoa, Italy.

Maurizio Miano (M)

UOC Ematologia, Istituto Giannina Gaslini, Genoa, Italy.

Antonio Risitano (A)

Università Federico II, Naples, Italy.

Marie Robin (M)

French reference center for aplastic anemia and PNH;Saint-Louis Hospital, Université de Paris, Paris, France.

Carlo Dufour (C)

UOC Ematologia, Istituto Giannina Gaslini, Genoa, Italy.

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