Genomics of Breast Cancer Brain Metastases: A Meta-Analysis and Therapeutic Implications

Author:

Nguyen Thuy Thi1234,Hamdan Diaddin25ORCID,Angeli Eurydice246,Feugeas Jean-Paul78,Le Quang Van12,Pamoukdjian Frédéric249ORCID,Bousquet Guilhem246ORCID

Affiliation:

1. National Cancer Hospital, Ha Noi 100000, Vietnam

2. Institut National de la Santé Et de la Recherche Médicale (INSERM), Université Paris Cité, UMR_S942 MASCOT, 75006 Paris, France

3. Department of Pediatrics, Hanoi Medical University, Ha Noi 100000, Vietnam

4. Institut Galilée, Université Sorbonne Paris Nord, 93439 Villetaneuse, France

5. Hôpital La Porte Verte, 78000 Versailles, France

6. Service d’Oncologie Médicale, Hôpital Avicenne, Assistance Publique Hôpitaux de Paris, 93000 Bobigny, France

7. INSERM U1098, 25030 Besançon, France

8. Laboratoire de Biochimie Hôpital Jean Minjoz, Université de Franche-Comté, 25000 Besançon, France

9. Service de Médecine Gériatrique, Hôpital Avicenne, Assistance Publique Hôpitaux de Paris, 93000 Bobigny, France

Abstract

Breast cancer brain metastases are a challenging daily practice, and the biological link between gene mutations and metastatic spread to the brain remains to be determined. Here, we performed a meta-analysis on genomic data obtained from primary tumors, extracerebral metastases and brain metastases, to identify gene alterations associated with metastatic processes in the brain. Articles with relevant findings were selected using Medline via PubMed, from January 1999 up to February 2022. A critical review was conducted according to the Preferred Reporting Items for Systematic Review and Meta-analysis statement (PRISMA). Fifty-seven publications were selected for this meta-analysis, including 37,218 patients in all, 11,906 primary tumor samples, 5541 extracerebral metastasis samples, and 1485 brain metastasis samples. We report the overall and sub-group prevalence of gene mutations, including comparisons between primary tumors, extracerebral metastases and brain metastases. In particular, we identified six genes with a higher mutation prevalence in brain metastases than in extracerebral metastases, with a potential role in metastatic processes in the brain: ESR1, ERBB2, EGFR, PTEN, BRCA2 and NOTCH1. We discuss here the therapeutic implications. Our results underline the added value of obtaining biopsies from brain metastases to fully explore their biology, in order to develop personalized treatments.

Funder

the University Sorbonne Paris Nord International Scholarship, Erasmus+ kit mobility

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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