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Does Pre-Emptive Availability of PREDICT 2.1 Results Change Ordering Practices for Oncotype DX? A Multi-Center Prospective Cohort Study.

Authors :
Awan, Arif Ali
Saunders, Deanna
Pond, Gregory
Hamm, Caroline
Califaretti, Nadia
Mates, Mihaela
Kumar, Vikaash
Ibrahim, Mohammed F. K.
Beltran-Bless, Ana-Alicia
Vandermeer, Lisa
Hilton, John
Clemons, Mark
Source :
Current Oncology. Mar2024, Vol. 31 Issue 3, p1278-1290. 13p.
Publication Year :
2024

Abstract

For early-stage hormone receptor (HR)-positive and HER2-negative breast cancer, tools to estimate treatment benefit include free and publicly available algorithms (e.g., PREDICT 2.1) and expensive molecular assays (e.g., Oncotype DX). There remains a need to identify patients who de-rive the most benefit from molecular assays and where this test may be of poor value. In this multicenter prospective cohort study, we evaluated whether use of PREDICT 2.1 would impact physician decision making. For the first 6 months of the study, data on physician use of both PREDICT 2.1 and Oncotype DX ordering were collected on all newly diagnosed patients eligible for molecular testing. After 6 months, an educational intervention was undertaken to see if providing physicians with PREDICT 2.1 results affects the frequency of Oncotype DX requests. A total of 602 patients across six cancer centers in Ontario, Canada were recruited between March 2020 and November 2021. Providing PREDICT 2.1 results and an educational intervention did not alter the ordering of an Oncotype DX. For patients with low clinical risk, either by clinico-pathologic features or by PREDICT 2.1, the probability of obtaining a high Oncotype DX recurrence score was substantially lower compared to patients with high-clinical-risk disease. The introduction of an educational intervention had no impact on molecular assay requests. However, routine ordering of molecular assays for patients with low-clinical-risk disease is of poor value. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11980052
Volume :
31
Issue :
3
Database :
Academic Search Index
Journal :
Current Oncology
Publication Type :
Academic Journal
Accession number :
176303309
Full Text :
https://doi.org/10.3390/curroncol31030096