BAM conditioning before autologous transplantation for lymphoma: a study on behalf of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC).


Journal

Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 20 11 2018
accepted: 21 04 2019
pubmed: 22 5 2019
medline: 26 7 2019
entrez: 22 5 2019
Statut: ppublish

Résumé

High-dose chemotherapy before autologous transplantation is a therapeutic option as consolidation in primary or relapsed lymphoma. Even if BEAM conditioning is generally used, alternative conditioning regimens have been published. The purpose of this study was to assess the outcome of 177 adult patients with lymphoma whose conditioning treatment included a BAM (busulfan, aracytine, and melphalan) regimen. With a median follow-up of 17.4 months, 2-year estimates of overall survival and progression-free survival for the entire group were 87% and 70.5%, respectively. Mucositis was the main reported complications and infectious episodes were described in 80.2% of patients. According to multivariate analysis, high performance status and age at diagnosis were adverse factors for survival and increased the risk of disease relapse and death. Despite its limitations, this retrospective study suggests that BAM combination is a valid conditioning regimen in lymphoma patients, with an acceptable rate of toxicity.

Identifiants

pubmed: 31111177
doi: 10.1007/s00277-019-03704-z
pii: 10.1007/s00277-019-03704-z
doi:

Substances chimiques

Cytarabine 04079A1RDZ
Busulfan G1LN9045DK
Melphalan Q41OR9510P

Types de publication

Journal Article

Langues

eng

Pagination

1973-1980

Auteurs

Jérôme Cornillon (J)

Department of Clinical Hematology, Institut de Cancérologie Lucien Neuwirth, Saint-Priest-en-Jarez, France. jerome.cornillon@icloire.fr.

Elisabeth Daguenet (E)

Department of Clinical Hematology, Institut de Cancérologie Lucien Neuwirth, Saint-Priest-en-Jarez, France.

Jacques-Olivier Bay (JO)

Centre Hospitalo-Universitaire Clermont-Ferrand, Clermont-Ferrand, France.

Adrien Chauchet (A)

Centre Hospitalier Régional Universitaire Besançon, Inserm UMR 1098, Besançon, France.

Gilles Salles (G)

Centre Hospitalier Lyon Sud, Lyon, France.

Nathalie Contentin (N)

Centre Henri Becquerel, Rouen, France.

Emmanuelle Nicolas-Virelizier (E)

Centre Léon Bérard, Lyon, France.

Mélanie Mercier (M)

Centre Hospitalo-Universitaire d'Angers, Angers, France.

Nicolas Vallet (N)

Centre Hospitalo-Universitaire Tours, Tours, France.

Magda Alexis (M)

Centre Hospitalier Régional Orléans, Orléans, France.

Marie-Lorraine Chrétien (ML)

Centre Hospitalo-Universitaire Dijon, Dijon, France.

Thomas Cluzeau (T)

Centre Hospitalo-Universitaire Nice, Nice, France.

Anne Huynh (A)

Centre Hospitalo-Universitaire Toulouse, Toulouse, France.

Chantal Himberlin (C)

Centre Hospitalo-Universitaire Reims, Reims, France.

Véronique Dorvaux (V)

Centre Hospitalier Régional Metz, Metz, France.

Sandy Amorim (S)

Département d'Onco-Hématologie adulte, Hôpital Saint-Louis AP-HP, Paris, France.

Caroline Lejeune (C)

Department of Clinical Hematology, Institut de Cancérologie Lucien Neuwirth, Saint-Priest-en-Jarez, France.

Régis Peffault de Latour (RP)

Département d'Hématologie Greffe, Hôpital Saint-Louis AP-HP, Paris, France.

Emmanuel Gyan (E)

Centre Hospitalo-Universitaire Tours, Tours, France.

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Classifications MeSH