Conditioning-based outcomes after allogeneic transplantation for myeloma following a prior autologous transplant (1991-2012) on behalf of EBMT CMWP.


Journal

European journal of haematology
ISSN: 1600-0609
Titre abrégé: Eur J Haematol
Pays: England
ID NLM: 8703985

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 21 10 2019
revised: 10 11 2019
accepted: 12 11 2019
pubmed: 19 11 2019
medline: 3 10 2020
entrez: 19 11 2019
Statut: ppublish

Résumé

The aim of this study was to compare the effect of the intensity of conditioning approaches used in allogeneic transplantation in myeloma-reduced intensity conditioning (RIC), non-myeloablative (NMA), myeloablative conditioning (MAC) or Auto-AlloHCT-on outcomes in patients who had had a prior autologous transplant. A retrospective analysis of the EBMT database (1991-2012) was performed. A total of 344 patients aged between 40 and 60 years at the time of alloHCT were identified: 169 RIC, 69 NMA, 65 MAC and 41 Auto-Allo transplants. At a median follow-up of 54 months, the probabilities of overall survival (OS) at 5 years were 39% (95% CI 31%-47%), 45% (95% CI 32%-57%), 19% (95% CI 6%-32%) and 34% (95% CI 17%-51%), respectively. Status at allogeneic HCT other than CR or PR conferred a 70% higher risk of death and a 40% higher risk of relapse. OS was markedly lower in the MAC group (P = .004). MAC alloHCT was associated with a higher risk of death than RIC alloHCT until 2002 (HR = 4.1, P < .001) but not after 2002 (HR = 1.2, P = .276). From 1991 to 2002, MAC was associated with poorer OS. Between 2003 and 2012, there were no significant differences in outcomes based on these different approaches.

Identifiants

pubmed: 31737951
doi: 10.1111/ejh.13352
doi:

Types de publication

Historical Article Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

181-189

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Références

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Auteurs

Patrick J Hayden (PJ)

Dept. of Haematology, Trinity College Dublin, St. James's Hospital, Dublin, Ireland.

Simona Iacobelli (S)

Tor Vergata University of Rome, Rome, Italy.

José Antonio Pérez-Simón (JA)

Hospital Universitario Virgen del Rocio, Instituto de Biomedicina y Universidad de Sevilla (IBIS)/CSIC/CIBERONC, Seville, Spain.

Anja van Biezen (A)

Leiden EBMT Data Office, Leiden, Netherlands.

Monique Minnema (M)

University Medical Centre Utrecht, Utrecht, Netherlands.

Riitta Niittyvuopio (R)

HUCH Comprehensive Cancer Center, Helsinki, Finland.

Stefan Schönland (S)

University of Heidelberg, Heidelberg, Germany.

Ellen Meijer (E)

VU University Medical Center, Amsterdam, Netherlands.

Didier Blaise (D)

Centre de Recherche en Cancérologie de Marseille Institut Paoli Calmettes, Marseille, France.

Noel Milpied (N)

CHU Bordeaux Hôpital Haut-leveque, Pessac, France.

Francisco J Márquez-Malaver (FJ)

Hospital Universitario Virgen del Rocio, Instituto de Biomedicina y Universidad de Sevilla (IBIS)/CSIC/CIBERONC, Seville, Spain.

Joan Hendrik Veelken (JH)

Leiden University Medical Centre, Leiden, Netherlands.

Johan Maertens (J)

University Hospital Gasthuisberg, Leuven, Belgium.

Mauricette Michallet (M)

Centre Hospitalier Lyon-Sud, Lyon, France.

Jörg Cammenga (J)

Linköping University Hospital, Linköping, Sweden.

Stephanie N'Guyen (S)

Hopital la Pitié-Salpêtrière, Paris, France.

Dietger Niederwieser (D)

University Hospital Leipzig, Leipzig, Germany.

Mathilde Hunault-Berger (M)

CHRU Angers, Angers, France.

Jean Henri Bourhis (JH)

Gustave Roussy institut de cancérologie, Villejuif, France.

Jakob Passweg (J)

University Hospital of Basel, Basel, Switzerland.

Arancha Bermudez (A)

FEA Servicio de Hematología, Santander, Spain.

Yves Chalandon (Y)

Hôpitaux Universitaires de Genève and Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Ibrahim Yakoub-Agha (I)

Hôpital Claude Huriez, Lille, France.

Laurent Garderet (L)

Hospital Saint Antoine, Paris, France.

Nicolaus Kröger (N)

University Hospital Eppendorf, Hamburg, Germany.

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