Azithromycin Use and Increased Cancer Risk among Patients with Bronchiolitis Obliterans after Hematopoietic Cell Transplantation.


Journal

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628

Informations de publication

Date de publication:
02 2020
Historique:
received: 16 08 2019
revised: 08 10 2019
accepted: 25 10 2019
pubmed: 5 11 2019
medline: 24 6 2021
entrez: 5 11 2019
Statut: ppublish

Résumé

Azithromycin exposure during the early phase of allogeneic hematopoietic cell transplantation (HCT) has been associated with an increased incidence of hematologic relapse. We assessed the impact of azithromycin exposure on the occurrence of relapse or new subsequent neoplasm (SN) in patients with bronchiolitis obliterans syndrome (BOS) after HCT who are commonly treated with azithromycin alone or in combination with other agents. In a retrospective study of patients with BOS from 2 large allograft centers, the effect of azithromycin exposure on the risk of relapse or SN was estimated from a Cox model with a time-dependent variable for treatment initiation. The Cox model was adjusted on time-fixed covariates measured at cohort entry, selected for their potential prognostic value. Similar models were used to assess the exposure effect on the cause-specific hazard of relapse, SN, and death free of those events. Sensitivity analyses were performed using propensity score matching. Among 316 patients, 227 (71.8%) were exposed to azithromycin after BOS diagnosis. The corresponding adjusted hazard ratio (HR) in patients exposed to azithromycin versus unexposed was 1.51 (95% confidence interval [CI], 0.90 to 2.55) for relapse or SN, 0.82 (95% CI, 0.37 to 1.83) for relapse, and 2.00 (95% CI, 1.01 to 3.99) for SN. Patients exposed to azithromycin had a significantly lower cause-specific hazard of death free of neoplasm and relapse (adjusted HR, 0.54; 95% CI, 0.34 to 0.89). In conclusion, exposure to azithromycin after BOS after HCT was associated with an increased risk of SN but not relapse.

Identifiants

pubmed: 31682980
pii: S1083-8791(19)30707-4
doi: 10.1016/j.bbmt.2019.10.025
pmc: PMC7430235
mid: NIHMS1612041
pii:
doi:

Substances chimiques

Azithromycin 83905-01-5

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

392-400

Subventions

Organisme : NCI NIH HHS
ID : P01 CA018029
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA015704
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA223498
Pays : United States

Informations de copyright

Copyright © 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

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Auteurs

Guang-Shing Cheng (GS)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington.

Louise Bondeelle (L)

AP-HP, Université de Paris, Hôpital Saint-Louis, Service de Pneumologie, Paris, France.

Ted Gooley (T)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Qianchuan He (Q)

Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Kareem Jamani (K)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Elizabeth F Krakow (EF)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Medical Oncology, Department of Medicine, University of Washington, Seattle, Washington.

Mary E D Flowers (MED)

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Medical Oncology, Department of Medicine, University of Washington, Seattle, Washington.

Régis Peffault de Latour (RP)

AP-HP, Hématologie-Transplantation Hôpital St Louis, Université de Paris, Paris, France.

David Michonneau (D)

AP-HP, Hématologie-Transplantation Hôpital St Louis, Université de Paris et INSERM UMR 1160, Paris, France.

Gérard Socié (G)

AP-HP, Hématologie-Transplantation Hôpital St Louis, Université de Paris et INSERM UMR 1160, Paris, France.

Jason W Chien (JW)

Infectious Diseases Therapeutic Area, Janssen Biopharma, South San Francisco, California.

Sylvie Chevret (S)

AP-HP, Hôpital Saint-Louis, Service de Biostatistique et Information Médicale, Paris, France; Université de Paris, ECSTRRA, UMR 1153 CRESS, Biostatistics and Clinical Epidemiology Research Team, Paris, France.

Anne Bergeron (A)

AP-HP, Université de Paris, Hôpital Saint-Louis, Service de Pneumologie, Paris, France; Université de Paris, ECSTRRA, UMR 1153 CRESS, Biostatistics and Clinical Epidemiology Research Team, Paris, France. Electronic address: anne.bergeron-lafaurie@aphp.fr.

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