Literature DB >> 32923853

Identifying ERBB2 Activating Mutations in HER2-Negative Breast Cancer: Clinical Impact of Institute-Wide Genomic Testing and Enrollment in Matched Therapy Trials.

Pedro Exman1, Ana C Garrido-Castro1, Melissa E Hughes1, Rachel A Freedman1, Tianyu Li1, Lorenzo Trippa1, Brittany L Bychkovsky1, Romualdo Barroso-Sousa1, Simona Di Lascio1, Colin Mackichan1, Max R Lloyd1, Max Krevalin1, Ethan Cerami1, Margaret S Merrill1, Rebecca Santiago1, Lindsey Crowley1, Nicole Kuhnly1, Janet Files1, Neal I Lindeman1, Laura E MacConaill2, Priti Kumari1, Sara M Tolaney1, Ian E Krop1, Ron Bose3, Bruce E Johnson1, Cynthia X Ma3, Deborah A Dillon1,2, Eric P Winer1, Nikhil Wagle1, Nancy U Lin1.   

Abstract

PURPOSE: The yield of comprehensive genomic profiling in recruiting patients to molecular-based trials designed for small subgroups has not been fully evaluated. We evaluated the likelihood of enrollment in a clinical trial that required the identification of a specific genomic change based on our institute-wide genomic tumor profiling. PATIENTS AND METHODS: Using genomic profiling from archived tissue samples derived from patients with metastatic breast cancer treated between 2011 and 2017, we assessed the impact of systematic genomic characterization on enrollment in an ongoing phase II trial (ClinicalTrials.gov identifier: NCT01670877). Our primary aim was to describe the proportion of patients with a qualifying ERBB2 mutation identified by our institutional genomic panel (OncoMap or OncoPanel) who enrolled in the trial. Secondary objectives included median time from testing result to trial registration, description of the spectrum of ERBB2 mutations, and survival. Associations were calculated using Fisher's exact test.
RESULTS: We identified a total of 1,045 patients with metastatic breast cancer without ERBB2 amplification who had available genomic testing results. Of these, 42 patients were found to have ERBB2 mutation and 19 patients (1.8%) were eligible for the trial on the basis of the presence of an activating mutation, 18 of which were identified by OncoPanel testing. Fifty-eight percent of potentially eligible patients were approached, and 33.3% of eligible patients enrolled in the trial guided exclusively by OncoPanel testing.
CONCLUSION: More than one half of eligible patients were approached for trial participation and, significantly, one third of those were enrolled in NCT01670877. Our data illustrate the ability to enroll patients in trials of rare subsets in routine clinical practice and highlight the need for these broadly based approaches to effectively support the success of these studies.
© 2019 by American Society of Clinical Oncology.

Entities:  

Year:  2019        PMID: 32923853      PMCID: PMC7446367          DOI: 10.1200/PO.19.00087

Source DB:  PubMed          Journal:  JCO Precis Oncol        ISSN: 2473-4284


  15 in total

1.  Genomic Characterization of Primary Invasive Lobular Breast Cancer.

Authors:  Christine Desmedt; Gabriele Zoppoli; Gunes Gundem; Giancarlo Pruneri; Denis Larsimont; Marco Fornili; Debora Fumagalli; David Brown; Françoise Rothé; Delphine Vincent; Naima Kheddoumi; Ghizlane Rouas; Samira Majjaj; Sylvain Brohée; Peter Van Loo; Patrick Maisonneuve; Roberto Salgado; Thomas Van Brussel; Diether Lambrechts; Ron Bose; Otto Metzger; Christine Galant; François Bertucci; Martine Piccart-Gebhart; Giuseppe Viale; Elia Biganzoli; Peter J Campbell; Christos Sotiriou
Journal:  J Clin Oncol       Date:  2016-02-29       Impact factor: 44.544

2.  Institutional implementation of clinical tumor profiling on an unselected cancer population.

Authors:  Lynette M Sholl; Khanh Do; Priyanka Shivdasani; Ethan Cerami; Adrian M Dubuc; Frank C Kuo; Elizabeth P Garcia; Yonghui Jia; Phani Davineni; Ryan P Abo; Trevor J Pugh; Paul van Hummelen; Aaron R Thorner; Matthew Ducar; Alice H Berger; Mizuki Nishino; Katherine A Janeway; Alanna Church; Marian Harris; Lauren L Ritterhouse; Joshua D Campbell; Vanesa Rojas-Rudilla; Azra H Ligon; Shakti Ramkissoon; James M Cleary; Ursula Matulonis; Geoffrey R Oxnard; Richard Chao; Vanessa Tassell; James Christensen; William C Hahn; Philip W Kantoff; David J Kwiatkowski; Bruce E Johnson; Matthew Meyerson; Levi A Garraway; Geoffrey I Shapiro; Barrett J Rollins; Neal I Lindeman; Laura E MacConaill
Journal:  JCI Insight       Date:  2016-11-17

3.  Feasibility of Large-Scale Genomic Testing to Facilitate Enrollment Onto Genomically Matched Clinical Trials.

Authors:  Funda Meric-Bernstam; Lauren Brusco; Kenna Shaw; Chacha Horombe; Scott Kopetz; Michael A Davies; Mark Routbort; Sarina A Piha-Paul; Filip Janku; Naoto Ueno; David Hong; John De Groot; Vinod Ravi; Yisheng Li; Raja Luthra; Keyur Patel; Russell Broaddus; John Mendelsohn; Gordon B Mills
Journal:  J Clin Oncol       Date:  2015-05-26       Impact factor: 44.544

4.  Activating HER2 mutations in HER2 gene amplification negative breast cancer.

Authors:  Ron Bose; Shyam M Kavuri; Adam C Searleman; Wei Shen; Dong Shen; Daniel C Koboldt; John Monsey; Nicholas Goel; Adam B Aronson; Shunqiang Li; Cynthia X Ma; Li Ding; Elaine R Mardis; Matthew J Ellis
Journal:  Cancer Discov       Date:  2012-12-07       Impact factor: 39.397

5.  Cancer Therapy Directed by Comprehensive Genomic Profiling: A Single Center Study.

Authors:  Jennifer J Wheler; Filip Janku; Aung Naing; Yali Li; Bettzy Stephen; Ralph Zinner; Vivek Subbiah; Siqing Fu; Daniel Karp; Gerald S Falchook; Apostolia M Tsimberidou; Sarina Piha-Paul; Roosevelt Anderson; Danxia Ke; Vincent Miller; Roman Yelensky; J Jack Lee; David S Hong; Razelle Kurzrock
Journal:  Cancer Res       Date:  2016-05-18       Impact factor: 12.701

6.  Neratinib Efficacy and Circulating Tumor DNA Detection of HER2 Mutations in HER2 Nonamplified Metastatic Breast Cancer.

Authors:  Cynthia X Ma; Ron Bose; Feng Gao; Rachel A Freedman; Melinda L Telli; Gretchen Kimmick; Eric Winer; Michael Naughton; Matthew P Goetz; Christy Russell; Debu Tripathy; Melody Cobleigh; Andres Forero; Timothy J Pluard; Carey Anders; Polly Ann Niravath; Shana Thomas; Jill Anderson; Caroline Bumb; Kimberly C Banks; Richard B Lanman; Richard Bryce; Alshad S Lalani; John Pfeifer; Daniel F Hayes; Mark Pegram; Kimberly Blackwell; Philippe L Bedard; Hussam Al-Kateb; Matthew J C Ellis
Journal:  Clin Cancer Res       Date:  2017-07-05       Impact factor: 12.531

7.  Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors.

Authors:  Shakti H Ramkissoon; Pratiti Bandopadhayay; Jaeho Hwang; Lori A Ramkissoon; Noah F Greenwald; Steven E Schumacher; Ryan O'Rourke; Nathan Pinches; Patricia Ho; Hayley Malkin; Claire Sinai; Mariella Filbin; Ashley Plant; Wenya Linda Bi; Michael S Chang; Edward Yang; Karen D Wright; Peter E Manley; Matthew Ducar; Sanda Alexandrescu; Hart Lidov; Ivana Delalle; Liliana C Goumnerova; Alanna J Church; Katherine A Janeway; Marian H Harris; Laura E MacConaill; Rebecca D Folkerth; Neal I Lindeman; Charles D Stiles; Mark W Kieran; Azra H Ligon; Sandro Santagata; Adrian M Dubuc; Susan N Chi; Rameen Beroukhim; Keith L Ligon
Journal:  Neuro Oncol       Date:  2017-07-01       Impact factor: 12.300

8.  HER2 somatic mutations are associated with poor survival in HER2-negative breast cancers.

Authors:  Tonghui Wang; Ye Xu; Shuyan Sheng; Hua Yuan; Tao Ouyang; Jinfeng Li; Tianfeng Wang; Zhaoqing Fan; Tie Fan; Benyao Lin; Yuntao Xie
Journal:  Cancer Sci       Date:  2017-04-21       Impact factor: 6.716

9.  Profiling critical cancer gene mutations in clinical tumor samples.

Authors:  Laura E MacConaill; Catarina D Campbell; Sarah M Kehoe; Adam J Bass; Charles Hatton; Lili Niu; Matt Davis; Keluo Yao; Megan Hanna; Chandrani Mondal; Lauren Luongo; Caroline M Emery; Alissa C Baker; Juliet Philips; Deborah J Goff; Michelangelo Fiorentino; Mark A Rubin; Kornelia Polyak; Jennifer Chan; Yuexiang Wang; Jonathan A Fletcher; Sandro Santagata; Gianni Corso; Franco Roviello; Ramesh Shivdasani; Mark W Kieran; Keith L Ligon; Charles D Stiles; William C Hahn; Matthew L Meyerson; Levi A Garraway
Journal:  PLoS One       Date:  2009-11-18       Impact factor: 3.240

10.  Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update.

Authors:  Antonio C Wolff; M Elizabeth H Hammond; David G Hicks; Mitch Dowsett; Lisa M McShane; Kimberly H Allison; Donald C Allred; John M S Bartlett; Michael Bilous; Patrick Fitzgibbons; Wedad Hanna; Robert B Jenkins; Pamela B Mangu; Soonmyung Paik; Edith A Perez; Michael F Press; Patricia A Spears; Gail H Vance; Giuseppe Viale; Daniel F Hayes
Journal:  J Clin Oncol       Date:  2013-10-07       Impact factor: 44.544

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  2 in total

1.  Genomic Characterization of de novo Metastatic Breast Cancer.

Authors:  Ana C Garrido-Castro; Liam F Spurr; Melissa E Hughes; Yvonne Y Li; Andrew D Cherniack; Priti Kumari; Maxwell R Lloyd; Brittany Bychkovsky; Romualdo Barroso-Sousa; Simona Di Lascio; Esha Jain; Janet Files; Ayesha Mohammed-Abreu; Max Krevalin; Colin MacKichan; William T Barry; Hao Guo; Daniel Xia; Ethan Cerami; Barrett J Rollins; Laura E MacConaill; Neal I Lindeman; Ian E Krop; Bruce E Johnson; Nikhil Wagle; Eric P Winer; Deborah A Dillon; Nancy U Lin
Journal:  Clin Cancer Res       Date:  2020-12-08       Impact factor: 13.801

Review 2.  HER2 Low, Ultra-low, and Novel Complementary Biomarkers: Expanding the Spectrum of HER2 Positivity in Breast Cancer.

Authors:  Konstantinos Venetis; Edoardo Crimini; Elham Sajjadi; Chiara Corti; Elena Guerini-Rocco; Giuseppe Viale; Giuseppe Curigliano; Carmen Criscitiello; Nicola Fusco
Journal:  Front Mol Biosci       Date:  2022-03-15
  2 in total

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