Cardiovascular Safety in Oncology Clinical Trials: JACC: CardioOncology Primer

Marc P. Bonaca*, Ninian N. Lang, Alice Chen, Laleh Amiri-Kordestani, Leslie Lipka, Michal Zwiewka, Colette Strnadova, Sigrid Klaar, Susan Dent, Tijana Krnjeta Janicijevic, Joerg Herrmann, Ana Barac, Rudolf A. de Boer, Anita Deswal, Morten Schou, Tomas G. Neilan, Peter van der Meer, Javid Moslehi, Lavanya Kondapalli, Bonnie KyTeresa Lopez Fernandez, R. Frank Cornell, Thomas W. Flaig, Judith Hsia, Elad Sharon, Evandro de Azambuja, Jonathan Seltzer, James L. Januzzi, Mark C. Petrie

*Corresponding author voor dit werk

Onderzoeksoutput: Review articlepeer review

3 Citaten (Scopus)
24 Downloads (Pure)

Samenvatting

The development of novel treatments has improved cancer outcomes but may result in cardiovascular toxicities. Traditional approaches to clinical trial safety evaluation have limitations in their ability to detect signals of cardiovascular risk. Mechanisms to increase power and specificity to clarify cardiovascular safety are required. However, implications include increased costs and slower development. The Cardiovascular Safety Research Consortium facilitated stakeholder discussions with representation from academia, industry, and regulators. A think tank was assembled with the aim of providing recommendations for improved collection and reporting of cardiovascular safety signals in oncology trials. Two working groups were formed. The first focuses on incorporation of consensus definitions of cardiovascular disease into the Common Terminology Criteria for Adverse Events used in oncology trial reporting. The second group considers methods for ascertainment and adjudication of cardiovascular events in cancer trials. The overarching aim of this primer is to improve understanding of the potential cardiovascular toxicities of cancer therapies.

Originele taal-2English
Pagina's (van-tot)83-95
Aantal pagina's13
TijdschriftJacc: cardiooncology
Volume7
Nummer van het tijdschrift2
DOI's
StatusPublished - feb.-2025

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