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Genomic Profiling of Patients With Metastatic Breast Cancer

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    Clinical Implications of Prospective Genomic Profiling of Patients With Metastatic Breast Cancer

    Hot off the press - Article Published in Metastatic Breast Cancer Journal Scan / Research · October 05, 2020.

    Dr Priscilla Brastianos with her Alliance Trial, would agree with the findings of this study over 5 years with 234 patients enrolled.
    The Alliance Interim data due 1st half 2021?

    https://hotcopper.com.au/data/attachments/2545/2545644-2042a8bd918cc8229b60485bb564c65c.jpg

    BACKGROUND
    Metastatic breast cancer remains incurable. Next-generation sequencing (NGS) offers the ability to identify actionable genomic alterations in tumours which may then be matched with targeted therapies, but the implementation and utility of this approach is not well defined for patients with metastatic breast cancer.
    METHODS
    We recruited patients with advanced breast cancer of any subtype for prospective targeted NGS of their most recent tumour samples, using a panel of 108 breast cancer-specific genes. Genes were classified as actionable or non-actionable using the European Society of Medical Oncology Scale for Clinical Actionability of Molecular Targets (ESCAT) guidelines.
    RESULTS
    Between February 2014 and May 2019, 322 patients were enrolled onto the study, with 72% (n = 234) of patients successfully sequenced (n = 357 samples). The majority (74%, n = 171) of sequenced patients were found to carry a potentially actionable alteration, the most common being a PIK3CA mutation. Forty-three percent (n = 74) of patients with actionable alterations were referred for a clinical trial or referred for confirmatory germline testing or had a change in therapy outside of clinical trials. We found alterations in AKT1, BRCA2, CHEK2, ESR1, FGFR1, KMT2C, NCOR1, PIK3CA and TSC2 to be significantly enriched in our metastatic population compared with primary breast cancers. Concordance between primary and metastatic samples for key driver genes (TP53, ERBB2 amplification) was > 75%. Additionally, we found that patients with a higher number of mutations had a significantly worse overall survival.
    CONCLUSION
    Genomic profiling of patients with metastatic breast cancer can have clinical implications and should be considered in all suitable patients.

    https://www.practiceupdate.com/c/105907/67/13/?elsca1=emc_enews_weekinreview&elsca2=email&elsca3=practiceupdate_metastaticbreastcancer&elsca4=metastaticbreastcancer&elsca5=newsletter&rid=NDQ3MTgxOTYwMzc4S0&lid=10332481


    Regards.

 
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