Literature DB >> 27489289

Individualized Molecular Analyses Guide Efforts (IMAGE): A Prospective Study of Molecular Profiling of Tissue and Blood in Metastatic Triple-Negative Breast Cancer.

Heather A Parsons1, Julia A Beaver1, Ashley Cimino-Mathews1, Siraj M Ali2, Jennifer Axilbund1, David Chu1, Roisin M Connolly1, Rory L Cochran1, Sarah Croessmann1, Travis A Clark2, Christopher D Gocke1, Stacie C Jeter1, Mark R Kennedy2, Josh Lauring1, Justin Lee1, Doron Lipson2, Vincent A Miller2, Geoff A Otto2, Gary L Rosner1, Jeffrey S Ross2, Shannon Slater1, Philip J Stephens2, Dustin A VanDenBerg1, Antonio C Wolff1, Lauren E Young2, Daniel J Zabransky1, Zhe Zhang1, Jane Zorzi1, Vered Stearns3, Ben H Park3.   

Abstract

PURPOSE: The clinical utility of next-generation sequencing (NGS) in breast cancer has not been demonstrated. We hypothesized that we could perform NGS of a new biopsy from patients with metastatic triple-negative breast cancer (TNBC) in a clinically actionable timeframe. EXPERIMENTAL
DESIGN: We planned to enroll 40 patients onto a prospective study, Individualized Molecular Analyses Guide Efforts (IMAGE), to evaluate the feasibility of obtaining a new biopsy of a metastatic site, perform NGS (FoundationOne), and convene a molecular tumor board to formulate treatment recommendations within 28 days. We collected blood at baseline and at time of restaging to assess cell-free circulating plasma tumor DNA (ptDNA).
RESULTS: We enrolled 26 women with metastatic TNBC who had received ≥1 line of prior chemotherapy, and 20 (77%) underwent NGS of a metastatic site biopsy. Twelve (60%) evaluable patients received treatment recommendations within 28 days of consent. The study closed after 20 patients underwent NGS, based on protocol-specified interim futility analysis. Three patients went on to receive genomically directed therapies. Twenty-four of 26 patients had genetic alterations successfully detected in ptDNA. Among 5 patients, 4 mutations found in tumor tissues were not identified in blood, and 4 mutations found in blood were not found in corresponding tumors. In 9 patients, NGS of follow-up blood samples showed 100% concordance with baseline blood samples.
CONCLUSIONS: This study demonstrates challenges of performing NGS on prospective tissue biopsies in patients with metastatic TNBC within 28 days, while also highlighting the potential use of blood as a more time-efficient and less invasive method of mutational assessment. Clin Cancer Res; 23(2); 379-86. ©2016 AACR. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27489289      PMCID: PMC5241251          DOI: 10.1158/1078-0432.CCR-16-1543

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  30 in total

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10.  Multifocal clonal evolution characterized using circulating tumour DNA in a case of metastatic breast cancer.

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Journal:  Nat Commun       Date:  2015-11-04       Impact factor: 14.919

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Review 3.  Precision Oncology Decision Support: Current Approaches and Strategies for the Future.

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Review 4.  The current status of the clinical utility of liquid biopsies in cancer.

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Review 5.  Liquid biopsy: unlocking the potentials of cell-free DNA.

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7.  Association of Cell-Free DNA Tumor Fraction and Somatic Copy Number Alterations With Survival in Metastatic Triple-Negative Breast Cancer.

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