A novel outpatient regimen in management of fluoropyrimidine-induced cardiotoxicity.


Journal

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372

Informations de publication

Date de publication:
Dec 2023
Historique:
medline: 30 11 2023
pubmed: 9 3 2023
entrez: 8 3 2023
Statut: ppublish

Résumé

Fluoropyrimidines (FP) are cornerstone drugs in the treatment of gastrointestinal (GI) malignancies. Cardiotoxicity secondary to an FP chemotherapy is a serious complication. There are no standardized guidelines on the treatment of FP induced cardiotoxicity which may result in interruption and even discontinuation of life saving treatment. We present our experience in FP rechallenge using a novel outpatient regimen based on our "up-front" triple agent antianginal protocol. We report the retrospective study of the patients with suspected FP induced cardiotoxicity. Patients meeting the criteria were selected by C3OD (curated cancer clinical outcomes database) at Kansas University Medical Center (KUMC). We identified all patients with gastrointestinal malignancies who had suspected FP induced cardiotoxicity from January 2015 to March 2022. We then included the patients who were rechallenged with planned fluoropyrimidine regimen utilizing the three drug KU-protocol. We utilized a novel regimen by repurposing the already FDA-approved anti-anginal drugs in a manner that minimizes the risk of hypotension and bradycardia. In this retrospective study, 10 patients with suspected fluoropyrimidine induced cardiotoxicity were included from January-2015 to March-2022 at KUMC. Out of 10 patients who were rechallenged utilizing KU-protocol, eight patients (80%) were able to complete the previously planned fluoropyrimidine regimen. None of the patients required ER visits or hospital admission due to cardiac symptoms during the rechallenge utilizing the KU-protocol. Utilizing our novel outpatient regimen, we have successfully and safely allowed re-challenge of FP chemotherapy with good tolerability and completion of the intended course of chemotherapy without recurrent morbidity.

Identifiants

pubmed: 36883259
doi: 10.1177/10781552231161822
doi:

Substances chimiques

Antimetabolites 0
Fluorouracil U3P01618RT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1951-1956

Déclaration de conflit d'intérêts

Declaration of Conflicting InterestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Anup Kasi (A)

Medical Oncology, The University of Kansas Medical Center, Kansas City, Kansas, USA.

Pramod Gaudel (P)

Hematology-Oncology Physician, Cancer Care Specialists of Illinois, Decatur, USA.

Manidhar Lekkala (M)

Hematology-Oncology Physician, The University of Kansas Cancer Center at St Francis Campus, Kansas, USA.

Raed Al-Rajabi (R)

Medical Oncology, The University of Kansas Medical Center, Kansas City, Kansas, USA.

Anwaar Saeed (A)

Medical Oncology, The University of Kansas Medical Center, Kansas City, Kansas, USA.

Weijing Sun (W)

Medical Oncology, The University of Kansas Medical Center, Kansas City, Kansas, USA.

Charles Porter (C)

Cardiovascular Medicine, The University of Kansas Medical Center, Kansas City, Kansas, USA.

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Classifications MeSH