A perspective on the development and lack of interchangeability of the breast cancer intrinsic subtypes
- PMID: 35853907
- PMCID: PMC9296605
- DOI: 10.1038/s41523-022-00451-9
A perspective on the development and lack of interchangeability of the breast cancer intrinsic subtypes
Conflict of interest statement
F.S. and F.B.-M. have no competing financial and non-financial interests. N.M.K. reports the following competing financial interests: advisory and consulting fees from Invitae, G1 Therapeutics, Beyond Spring, Spectrum, BMS, Sandoz, Seattle Genetics, and Total Health all outside the submitted work. As a non-financial competing interest, N.M.K. reports to be among the authors of past and the latest ASCO breast cancer biomarker guidelines updates. A.P. declares no competing non-financial interests but reports advisory and consulting fees from Roche, Pfizer, Novartis, Amgen, BMS, Puma, Oncolytics Biotech, MSD, Guardant Health, Peptomyc, and Lilly, lecture fees from Roche, Pfizer, Novartis, Amgen, BMS, Nanostring Technologies and Daiichi Sankyo, institutional financial interests from Boehringer, Novartis, Roche, Nanostring, Sysmex Europa GmbH, Medica Scientia inno. Research, SL, Celgene, Astellas, and Pfizer; a leadership role in Reveal Genomics, SL; and a patent PCT/EP2016/080056.
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                References
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    - Carey, L. et al. Abstract GS2-00: correlative analysis of overall survival by intrinsic subtype across the MONALEESA-2, -3, and -7 studies of ribociclib + endocrine therapy in patients with HR+/HER2− advanced breast cancer. Cancer Res. 82, GS2-00 (2022).
 
 
        