Comparison Between 5-Azacytidine Treatment and Allogeneic Stem-Cell Transplantation in Elderly Patients With Advanced MDS According to Donor Availability (VidazaAllo Study).


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 10 2021
Historique:
pubmed: 21 7 2021
medline: 15 12 2021
entrez: 20 7 2021
Statut: ppublish

Résumé

In contrast to 5-azacytidine (5-aza), allogeneic stem-cell transplantation (HSCT) represents a curative treatment strategy for patients with myelodysplastic syndromes (MDS), but therapy-related mortality (TRM) limits its broader use in elderly patients with MDS. The present prospective multicenter study compared HSCT following 5-aza pretreatment with continuous 5-aza treatment in patients with higher-risk MDS age 55-70 years. One hundred ninety patients with a median age of 63 years were enrolled. Patients received 4-6 cycles of 5-aza followed by HLA-compatible HSCT after reduced-intensity conditioning or by continuous 5-aza if no donor was identified. Twenty-eight patients did not fulfill inclusion criteria (n = 20), died (n = 2) withdrew informed consent (n = 5), or were excluded for an unknown reason (n = 1). 5-aza induction started in 162 patients, but only 108 (67%) were eligible for subsequent allocation to HSCT (n = 81) or continuation of 5-aza (n = 27) because of disease progression (n = 26), death (n = 12), or other reasons (n = 16). Seven percent died during 5-aza before treatment allocation. The cumulative incidence of TRM after HSCT at 1 year was 19%. The event-free survival and overall survival after 5-aza pretreatment and treatment allocation at 3 years were 34% (95% CI, 22 to 47) and 50% (95% CI, 39 to 61) after allograft and 0% and 32% (95% CI, 14 to 52) after continuous 5-aza treatment ( In older patients with MDS, reduced-intensity conditioning HSCT resulted in a significantly improved event-free survival in comparison with continuous 5-aza therapy. Bridging with 5-aza to HSCT before is associated with a considerable rate of dropouts because of progression, mortality, and adverse events.

Identifiants

pubmed: 34283629
doi: 10.1200/JCO.20.02724
doi:

Substances chimiques

Antimetabolites, Antineoplastic 0
Azacitidine M801H13NRU

Banques de données

ClinicalTrials.gov
['NCT01404741']
EudraCT
['2010-018467-42']

Types de publication

Clinical Trial, Phase II Comparative Study Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3318-3327

Commentaires et corrections

Type : CommentIn

Auteurs

Nicolaus Kröger (N)

University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Katja Sockel (K)

Medical Clinic and Policlinic 1, University Hospital "Carl Gustav Carus" Dresden, Dresden, Germany.

Christine Wolschke (C)

University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Wolfgang Bethge (W)

University Hospital Tübingen, Tübingen, Germany.

Richard F Schlenk (RF)

Department of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.
NCT-Trial Center, National Center of Tumor Diseases Heidelberg, German Cancer Research Center, Heidelberg, Germany.

Dominik Wolf (D)

Internal Medicine V, Medical University of Innsbruck, Innsbruck, Austria.
Tyrolean Cancer Research Institute, Innsbruck, Austria.
Medical Clinic III, University Clinic Bonn, Bonn, Germany.

Michael Stadler (M)

Hannover Medical School, Hannover, Germany.

Guido Kobbe (G)

University Hospital Düsseldorf, Medical Faculty, Heinrich-Heine University, Düsseldorf, Germany.

Gerald Wulf (G)

University Medical Center Göttingen, Göttingen, Germany.

Gesine Bug (G)

Department of Medicine 2, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Kerstin Schäfer-Eckart (K)

Department of Medicine 5, Paracelsus Private University Nuremberg, Nuremberg, Germany.

Christof Scheid (C)

Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn, University of Cologne, Cologne Düsseldorf, Germany.

Florian Nolte (F)

Department of Hematology and Oncology, University Hospital Mannheim, Mannheim, Germany.

Jan Krönke (J)

University Hospital Ulm, Ulm, Germany.

Matthias Stelljes (M)

University Medical Center Münster, Münster, Germany.

Dietrich Beelen (D)

University Medical Center Essen, Essen, Germany.

Marion Heinzelmann (M)

University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Detlef Haase (D)

University Medical Center Göttingen, Göttingen, Germany.

Hannes Buchner (H)

Staburo München, Statistical Consulting, Munich, Germany.

Gabriele Bleckert (G)

Staburo München, Statistical Consulting, Munich, Germany.

Aristoteles Giagounidis (A)

St Mary's Hospital, Düsseldorf, Germany.

Uwe Platzbecker (U)

Medical Clinic and Policlinic 1, University Hospital "Carl Gustav Carus" Dresden, Dresden, Germany.
University of Leipzig Medical Center, Leipzig, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH