Cardiovascular safety profile of taxanes and vinca alkaloids: 30 years FDA registry experience.


Journal

Open heart
ISSN: 2053-3624
Titre abrégé: Open Heart
Pays: England
ID NLM: 101631219

Informations de publication

Date de publication:
12 2021
Historique:
received: 07 09 2021
accepted: 29 11 2021
entrez: 25 12 2021
pubmed: 26 12 2021
medline: 3 2 2022
Statut: ppublish

Résumé

Antimicrotubular agents are among the most commonly used classes of chemotherapeutic agents, but the risk of cardiovascular adverse events (CVAEs) remains unclear. Our objective was to study the CVAEs associated with antimicrotubular agents. The Food and Drug Administration's Adverse Event Reporting System was used to study CVAEs in adults from 1990 to 2020. Reported single-agent (only taxane or vinca alkaloid) CVAEs were compared with combination therapy (with at least one of the four major cardiotoxic drugs: anthracycline, HER2Neu inhibitors, tyrosine kinase inhibitors and checkpoint inhibitors) using adjusted polytomous logistic regression. Over 30 years, 134 398 adverse events were reported, of which 18 426 (13.4%) were CVAEs, with 74.1% due to taxanes and 25.9% due to vinca alkaloids. In 30 years, there has been a reduction in the proportion of reported CVAEs for taxanes from 15% to 11.8% (Cochran-Armitage P-trends <0.001) with no significant change in the proportion of reported CVAEs for vinca alkaloids (9.2%-11.7%; P-trends=0.06). The proportion of reported CVAEs was lower in both taxane and vinca alkaloid monotherapy versus combination therapy (reporting OR=0.50 and 0.55, respectively). Anthracyclines and HER2Neu inhibitor combinations with taxanes or vinca alkaloids primarily drove the higher burden of combination CVAEs. Hypertension requiring hospitalisation and heart failure was significantly lower in monotherapy versus combination antimicrotubular agent therapy. Antimicrotubular agents are associated with CVAEs, especially in combination chemotherapy regimens. Based on this study, we suggest routine cardiovascular assessment of patients with cancer before initiating antimicrotubular agents in combination therapy.

Identifiants

pubmed: 34952868
pii: openhrt-2021-001849
doi: 10.1136/openhrt-2021-001849
pmc: PMC8710909
pii:
doi:

Substances chimiques

Taxoids 0
Vinca Alkaloids 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL142097
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR070029
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL134354
Pays : United States
Organisme : NCI NIH HHS
ID : K12 CA133250
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA016058
Pays : United States
Organisme : NIA NIH HHS
ID : R56 AG064895
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL126949
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL155890
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Akshee Batra (A)

Department of Medicine, University of Vermont Medical Center, Burlington, Vermont, USA.

Brijesh Patel (B)

Department of Cardiology, West Virginia University, Morgantown, West Virginia, USA.

Daniel Addison (D)

Cardio-Oncology Program, Division of Cardiology, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

Lauren A Baldassarre (LA)

Department of Cardiology, Yale School of Medicine, New Haven, Connecticut, USA.

Nihar Desai (N)

Department of Cardiology, Yale School of Medicine, New Haven, Connecticut, USA.

Neal Weintraub (N)

Cardio-Oncology Program, Division of Cardiology, Department of Internal Medicine, Augusta University Medical College of Georgia, Augusta, Georgia, USA.

Anita Deswal (A)

Department of Cardiology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Zeeshan Hussain (Z)

Harrington Heart and Vascular Institute, University Hospitals, Cleveland, Ohio, USA.

Sherry-Ann Brown (SA)

Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Sarju Ganatra (S)

Department of Cardiovascular Medicine, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.

Vivek Agarwala (V)

Department of Medical Oncology, Narayana Superspeciality Hospital-Howrah, Howrah, West Bengal, India.

Purvish M Parikh (PM)

Mumbai Oncocare Centers, Mumbai, Maharashtra, India.

Michael Fradley (M)

Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

Arjun Ghosh (A)

Barts and The London NHS Trust, London, UK.

Avirup Guha (A)

Cardio-Oncology Program, Division of Cardiology, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA avirup.guha@gmail.com.
Cardio-Oncology Program, Division of Cardiology, Department of Internal Medicine, Augusta University Medical College of Georgia, Augusta, Georgia, USA.
Department of Internal Medicine, Case Western Reserve University, Cleveland, Ohio, USA.

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