Literature DB >> 35135159

Use of Next-Generation Sequencing Tests to Guide Cancer Treatment: Results From a Nationally Representative Survey of Oncologists in the United States.

Andrew N Freedman1, Carrie N Klabunde1, Kristine Wiant1, Lindsey Enewold1, Stacy W Gray1, Kelly K Filipski1, Nancy L Keating1, Debra G B Leonard1, Tracy Lively1, Timothy S McNeel1, Lori Minasian1, Arnold L Potosky1, Donna R Rivera1, Richard L Schilsky1, Deborah Schrag1, Naoko I Simonds1, Helmneh M Sineshaw1, Jeffery P Struewing1, Gordon Willis1, Janet S de Moor1.   

Abstract

PURPOSE: There are no nationally representative data on oncologists' use of next-generation sequencing (NGS) testing in practice. The purpose of this study was to investigate how oncologists in the United States use NGS tests to evaluate patients with cancer and to inform treatment recommendations.
METHODS: The study used data from the National Survey of Precision Medicine in Cancer Treatment, which was mailed to a nationally representative sample of oncologists in 2017 (N = 1,281; cooperation rate = 38%). Weighted percentages were calculated to describe NGS test use. Multivariable modeling was conducted to assess the association of test use with oncologist practice characteristics.
RESULTS: Overall, 75.6% of oncologists reported using NGS tests to guide treatment decisions. Of these oncologists, 34.0% used them often to guide treatment decisions for patients with advanced refractory disease, 29.1% to determine eligibility for clinical trials, and 17.5% to decide on off-label use of Food and Drug Administration-approved drugs. NGS test results informed treatment recommendations often for 26.8%, sometimes for 52.4%, and never or rarely for 20.8% of oncologists. Oncologists younger than 50 years of age, holding a faculty appointment, having genomics training, seeing more than 50 unique patients per month, and having access to a molecular tumor board were more likely to use NGS tests.
CONCLUSION: In 2017, most oncologists in the United States were using NGS tests to guide treatment decisions for their patients. More research is needed to establish the clinical usefulness of these tests, to develop evidence-based clinical guidelines for their use in practice, and to ensure that patients who can benefit from these new technologies receive appropriate testing and treatment.

Entities:  

Year:  2018        PMID: 35135159     DOI: 10.1200/PO.18.00169

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


  15 in total

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Journal:  PLoS One       Date:  2022-03-16       Impact factor: 3.240

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Authors:  Natalie M Reizine; Peter H O'Donnell
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Journal:  Cancer       Date:  2022-01-28       Impact factor: 6.921

6.  Pharmacogenomic testing and prescribing patterns for patients with cancer in a large national precision medicine cohort.

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Journal:  J Pers Med       Date:  2022-01-31

Review 8.  Clinical actionability of molecular targets in endometrial cancer.

Authors:  Mary Ellen Urick; Daphne W Bell
Journal:  Nat Rev Cancer       Date:  2019-08-06       Impact factor: 60.716

9.  High-level gain of mesenchymal-epithelial transition factor (MET) copy number using next-generation sequencing as a predictive biomarker for MET inhibitor efficacy.

Authors:  Shibo Wu; Guodong Li; Xin Zhao; Jianxing Xiang; Analyn Lizaso; Junyi Ye; Chunlei Shi; Lingxiang Chen
Journal:  Ann Transl Med       Date:  2020-06

10.  Liquid Biopsy-based Precision Therapy in Patients with Advanced Solid Tumors: A Real-world Experience from a Community-based Oncology Practice.

Authors:  Khalil Choucair; Bassam Ibrahim Mattar; Quoc Van Truong; Travis Koeneke; Phu Van Truong; Christopher Dakhil; Michael W Cannon; Seth Joel Page; Jeremy Michael Deutsch; Eric Carlson; Dennis Frederic Moore; Nassim H Nabbout; K James Kallail; Shaker R Dakhil; Pavan S Reddy
Journal:  Oncologist       Date:  2022-03-11
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