Effect of cross-platform gene-expression, computational methods on breast cancer subtyping in PALOMA-2 and PALLET studies.
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Embargo End Date
ICR Authors
Authors
Cheang, MCU
Rimawi, M
Johnston, S
Jacobs, SA
Bliss, J
Pogue-Geile, K
Kilburn, L
Zhu, Z
Schuster, EF
Xiao, H
Swaim, L
Deng, S
Lu, DR
Gauthier, E
Tursi, J
Slamon, DJ
Rugo, HS
Finn, RS
Liu, Y
Rimawi, M
Johnston, S
Jacobs, SA
Bliss, J
Pogue-Geile, K
Kilburn, L
Zhu, Z
Schuster, EF
Xiao, H
Swaim, L
Deng, S
Lu, DR
Gauthier, E
Tursi, J
Slamon, DJ
Rugo, HS
Finn, RS
Liu, Y
Document Type
Journal Article
Date
2024-06-29
Date Accepted
2024-06-14
Abstract
Intrinsic breast cancer molecular subtyping (IBCMS) provides significant prognostic information for patients with breast cancer and helps determine treatment. This study compared IBCMS methods on various gene-expression platforms in PALOMA-2 and PALLET trials. PALOMA-2 tumor samples were profiled using EdgeSeq and nanostring and subtyped with AIMS, PAM50, and research-use-only (ruo)Prosigna. PALLET tumor biopsies were profiled using mRNA sequencing and subtyped with AIMS and PAM50. In PALOMA-2 (nā=ā222), a 54% agreement was observed between results from AIMS and gold-standard ruoProsigna, with AIMS assigning 67% basal-like to HER2-enriched. In PALLET (nā=ā224), a 69% agreement was observed between results from PAM50 and AIMS. Different IBCMS methods may lead to different results and could misguide treatment selection; hence, a standardized clinical PAM50 assay and computational approach should be used.Trial number: NCT01740427.
Citation
npj Breast Cancer, 2024, 10 (1), pp. 54 -
Source Title
npj Breast Cancer
Publisher
NATURE PORTFOLIO
ISSN
2374-4677
eISSN
2374-4677
2374-4677
2374-4677
Collections
Research Team
Clin Trials & Stats Unit
