Association Between Granulocyte Colony-Stimulating Factor (G-CSF) Use and Myelodysplastic Syndrome (MDS) or Acute Myeloid Leukemia (AML) Among Elderly Patients with Breast, Lung, or Prostate Cancer.


Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
06 2022
Historique:
received: 01 02 2022
accepted: 17 03 2022
pubmed: 18 4 2022
medline: 25 5 2022
entrez: 17 4 2022
Statut: ppublish

Résumé

Patients diagnosed with cancer have an increased risk both for myelodysplastic syndromes (MDS) and for acute myeloid leukemia (AML) following treatment. Using SEER-Medicare data, we selected patients aged 66 years and older who completed systemic therapy between 2002 and 2014 for breast (stage I-III), lung (stage I-III), or prostate (stage I-IV) cancer. For each cancer, we estimated the risk of a composite endpoint of MDS or AML in patients receiving granulocyte colony-stimulating factor (G-CSF) vs. not. The 10-year cumulative risk difference (granulocyte colony-stimulating factor [G-CSF] - no G-CSF) for MDS-AML was 0.45% (95% CI 0.13-0.77%) in breast cancer and 0.39% (95% CI 0.15-0.62%) in lung cancer. G-CSF use was associated with a hazard ratio of 1.60 (95% CI 1.07-2.40) in breast cancer and 1.50 (95% CI 0.99-2.29) in lung cancer. Filgrastim use was associated with a hazard ratio of 1.01 (95% CI 1.00-1.03) per administration in breast cancer and 1.02 (95% CI 0.99-1.05) per administration in lung cancer. Pegfilgrastim was associated with a hazard ratio of 1.08 (95% CI 1.01-1.15) per administration in breast cancer and 1.12 (95% CI 1.00-1.25) per administration in lung cancer. Analyses in prostate cancer were limited because of the low number of events. The use of G-CSF in patients diagnosed with breast and lung cancer is associated with an increased risk of MDS-AML. However, the MDS-AML absolute risk difference is very low.

Identifiants

pubmed: 35430673
doi: 10.1007/s12325-022-02141-1
pii: 10.1007/s12325-022-02141-1
doi:

Substances chimiques

Granulocyte Colony-Stimulating Factor 143011-72-7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

2778-2795

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Healthcare Ltd., part of Springer Nature.

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Auteurs

Mark D Danese (MD)

Outcomes Insights, Inc., 30200 Agoura Road, Suite 230, Agoura Hills, CA, 91301, USA. mark@outins.com.

Jennifer Schenfeld (J)

Center for Observational Research, Amgen, Thousand Oaks, CA, USA.

Jaime Shaw (J)

Center for Observational Research, Amgen, Thousand Oaks, CA, USA.

Prasad Gawade (P)

Vertex Pharmaceuticals, Boston, MA, USA.

Akhila Balasubramanian (A)

Center for Observational Research, Amgen, Thousand Oaks, CA, USA.

Michael Kelsh (M)

Center for Observational Research, Amgen, Thousand Oaks, CA, USA.

Rohini K Hernandez (RK)

Center for Observational Research, Amgen, Thousand Oaks, CA, USA.

Gary Lyman (G)

Hutchinson Institute for Cancer Outcomes Research (HICOR), Fred Hutchinson, Seattle, WA, USA.

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