International research to address the challenges of metastatic breast cancer: the AURORA Program (BIG 14-01)
- PMID: 37221256
- PMCID: PMC10205751
- DOI: 10.1038/s41523-023-00548-9
International research to address the challenges of metastatic breast cancer: the AURORA Program (BIG 14-01)
Abstract
Despite recent advances in breast cancer research, we still know little about the mechanisms that lead to metastatic breast cancer (MBC). However, treatment options for patients have increased based on results of recent randomized clinical trials in this setting. Today we have much hope, yet many questions remain unanswered. Conducting a fully academic and international study such as AURORA is very challenging, yet ever more crucial to advancing knowledge about MBC.
Conflict of interest statement
The authors declare competing financial and non-financial interests. C.C., A.I. and T.G. have competing financial interests, as they are employed by Breast International Group (BIG), sponsor of the AURORA program. D.C. has a non-financial competing interest as the Chair of BIG and a competing financial interest since his institution is participating in AURORA with him as the principal investigator. L.N. has a financial competing interest as the Founding Scientific Director of BCRF, the primary funder of the AURORA Program. M.P. has a competing non-financial interest as the Founder and Past Chair of BIG, and one of the principal investigators of AURORA. She has a competing financial interest as the grant recipient for AURORA and her institution is participating in the program.
Figures



Similar articles
-
Aurora kinase A as a possible marker for endocrine resistance in early estrogen receptor positive breast cancer.Acta Oncol. 2018 Jan;57(1):67-73. doi: 10.1080/0284186X.2017.1404126. Epub 2017 Dec 4. Acta Oncol. 2018. PMID: 29202611 Clinical Trial.
-
Antineoplastic effects of an Aurora B kinase inhibitor in breast cancer.Mol Cancer. 2010 Feb 22;9:42. doi: 10.1186/1476-4598-9-42. Mol Cancer. 2010. PMID: 20175926 Free PMC article.
-
Aurora B induces epithelial-mesenchymal transition by stabilizing Snail1 to promote basal-like breast cancer metastasis.Oncogene. 2020 Mar;39(12):2550-2567. doi: 10.1038/s41388-020-1165-z. Epub 2020 Jan 29. Oncogene. 2020. PMID: 31996785
-
Promising Therapy in Lung Cancer: Spotlight on Aurora Kinases.Cancers (Basel). 2020 Nov 14;12(11):3371. doi: 10.3390/cancers12113371. Cancers (Basel). 2020. PMID: 33202573 Free PMC article. Review.
-
The Breast International Group 1-98 trial: big results for women with hormone-sensitive early breast cancer.Expert Rev Anticancer Ther. 2007 May;7(5):627-34. doi: 10.1586/14737140.7.5.627. Expert Rev Anticancer Ther. 2007. PMID: 17492927 Review.
Cited by
-
Treatment Sequencing in Metastatic HR+/HER2- Breast Cancer: A Delphi Consensus.Cancers (Basel). 2025 Apr 23;17(9):1412. doi: 10.3390/cancers17091412. Cancers (Basel). 2025. PMID: 40361341 Free PMC article. Review.
-
Gene expression in metastatic breast cancer-patterns in primary tumors and metastatic tissue with prognostic potential.Front Mol Biosci. 2024 Feb 21;10:1343979. doi: 10.3389/fmolb.2023.1343979. eCollection 2023. Front Mol Biosci. 2024. PMID: 38449790 Free PMC article.
-
Was kommt nach CDK4/6-Inhibition? Perspektiven beim fortgeschrittenen Mammakarzinom.Wien Klin Wochenschr. 2025 Aug;137(Suppl 6):219-232. doi: 10.1007/s00508-025-02582-y. Epub 2025 Jul 31. Wien Klin Wochenschr. 2025. PMID: 40742511 Free PMC article. German. No abstract available.
-
Clinical applications of next-generation sequencing-based ctDNA analyses in breast cancer: defining treatment targets and dynamic changes during disease progression.Mol Oncol. 2025 Jul;19(7):1897-1917. doi: 10.1002/1878-0261.13671. Epub 2024 Jun 12. Mol Oncol. 2025. PMID: 38867388 Free PMC article. Review.
-
Advancing breast cancer therapy in the era of molecular diagnostics.Breast. 2025 Aug;82:104488. doi: 10.1016/j.breast.2025.104488. Epub 2025 May 8. Breast. 2025. PMID: 40424679 Free PMC article. Review.
References
Grants and funding
LinkOut - more resources
Full Text Sources