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Circulating tumor DNA as an early cancer detection tool

Pharmacology & therapeutics (Oxford), 2020-03, Vol.207, p.107458-107458, Article 107458

2020

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Oncologists’ and cancer patients’ views on whole-exome sequencing and incidental findings: results from the CanSeq study

Genetics in medicine, 2016-10, Vol.18 (10), p.1011-1019

2016

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Combined Use of ALK Immunohistochemistry and FISH for Optimal Detection of ALK-Rearranged Lung Adenocarcinomas

Journal of thoracic oncology, 2013-03, Vol.8 (3), p.322-328

2013

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Anti-PD-1 Inhibitor-Related Pneumonitis in Non-Small Cell Lung Cancer

Cancer immunology research, 2016-04, Vol.4 (4), p.289-293

2016

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Factors influencing cancer genetic somatic mutation test ordering by cancer physician

Journal of translational medicine, 2020-11, Vol.18 (1), p.431-431, Article 431

2020

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Personal Genomic Testing for Cancer Risk: Results From the Impact of Personal Genomics Study

Journal of clinical oncology, 2017-02, Vol.35 (6), p.636-644

2017

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Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

Genetics in medicine, 2013-11, Vol.15 (11), p.860-867

2013

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Somatic Genomic Testing in Patients With Metastatic or Advanced Cancer: ASCO Provisional Clinical Opinion

Journal of clinical oncology, 2022-04, Vol.40 (11), p.1231-1258

2022

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Physicians' Attitudes About Multiplex Tumor Genomic Testing

Journal of clinical oncology, 2014-05, Vol.32 (13), p.1317-1323

2014

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Seeking Cancer-Related Information From Media and Family/Friends Increases Fruit and Vegetable Consumption Among Cancer Patients

Health communication, 2012-05, Vol.27 (4), p.380-388

2012

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Liquid Biopsy Screening for Early Detection of Lung Cancer: Current State and Future Directions

Clinical lung cancer, 2023-05, Vol.24 (3), p.209-217

2023

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Factors contributing to disparities in mortality among patients with non–small‐cell lung cancer

Cancer medicine (Malden, MA), 2018-11, Vol.7 (11), p.5832-5842

2018

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Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories

JNCI : Journal of the National Cancer Institute, 2016-04, Vol.108 (4), p.1

2016

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Private Payer and Medicare Coverage for Circulating Tumor DNA Testing: A Historical Analysis of Coverage Policies From 2015 to 2019

Journal of the National Comprehensive Cancer Network, 2020-07, Vol.18 (7), p.866-872

2020

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Identification of Incidental Germline Mutations in Patients With Advanced Solid Tumors Who Underwent Cell-Free Circulating Tumor DNA Sequencing

Journal of clinical oncology, 2018-12, Vol.36 (35), p.JCO1800328-3465

2018

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Demystifying the estimand framework: a case study using patient-reported outcomes in oncology

The lancet oncology, 2020-10, Vol.21 (10), p.e488-e494

2020

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Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry

JNCI : Journal of the National Cancer Institute, 2018-10, Vol.110 (10), p.1059-1066

2018

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Recall of Genomic Testing Results Among Patients with Cancer

The oncologist (Dayton, Ohio), 2021-12, Vol.26 (12), p.e2302-e2305

2021

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Preparing for the Unexpected: Recommendations for Returning Secondary Findings in Late-Stage Cancer Care

Genetics in medicine, 2024-01, Vol.26 (1), p.100991, Article 100991

2024

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Carboplatin and paclitaxel with vs without bevacizumab in older patients with advanced non-small cell lung cancer

JAMA : the journal of the American Medical Association, 2012-04, Vol.307 (15), p.1593

2012

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Risk Information Exposure and Direct-to-Consumer Genetic Testing for BRCA Mutations among Women with a Personal or Family History of Breast or Ovarian Cancer

Cancer epidemiology, biomarkers & prevention, 2009-04, Vol.18 (4), p.1303-1311

2009

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Attitudes Toward Research Participation and Investigator Conflicts of Interest Among Advanced Cancer Patients Participating in Early Phase Clinical Trials

Journal of clinical oncology, 2007-08, Vol.25 (23), p.3488-3494

2007

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Private Payer and Medicare Coverage Policies for Use of Circulating Tumor DNA Tests in Cancer Diagnostics and Treatment

Journal of the National Comprehensive Cancer Network, 2023-06, Vol.21 (6), p.609-616.e4

2023

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Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies

Genetics in medicine, 2019-12, Vol.21 (12), p.2781-2790

2019

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Circulating tumor DNA as an early cancer detection tool

Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine

Oncologists’ and cancer patients’ views on whole-exome sequencing and incidental findings: results from the CanSeq study

Combined Use of ALK Immunohistochemistry and FISH for Optimal Detection of ALK-Rearranged Lung Adenocarcinomas

Anti-PD-1 Inhibitor-Related Pneumonitis in Non-Small Cell Lung Cancer

Factors influencing cancer genetic somatic mutation test ordering by cancer physician

Personal Genomic Testing for Cancer Risk: Results From the Impact of Personal Genomics Study

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

Somatic Genomic Testing in Patients With Metastatic or Advanced Cancer: ASCO Provisional Clinical Opinion

Physicians' Attitudes About Multiplex Tumor Genomic Testing

Seeking Cancer-Related Information From Media and Family/Friends Increases Fruit and Vegetable Consumption Among Cancer Patients

Liquid Biopsy Screening for Early Detection of Lung Cancer: Current State and Future Directions

Factors contributing to disparities in mortality among patients with non–small‐cell lung cancer

Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories

Private Payer and Medicare Coverage for Circulating Tumor DNA Testing: A Historical Analysis of Coverage Policies From 2015 to 2019

Identification of Incidental Germline Mutations in Patients With Advanced Solid Tumors Who Underwent Cell-Free Circulating Tumor DNA Sequencing

Demystifying the estimand framework: a case study using patient-reported outcomes in oncology

Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry

Recall of Genomic Testing Results Among Patients with Cancer

Preparing for the Unexpected: Recommendations for Returning Secondary Findings in Late-Stage Cancer Care

Carboplatin and paclitaxel with vs without bevacizumab in older patients with advanced non-small cell lung cancer

Risk Information Exposure and Direct-to-Consumer Genetic Testing for BRCA Mutations among Women with a Personal or Family History of Breast or Ovarian Cancer

Attitudes Toward Research Participation and Investigator Conflicts of Interest Among Advanced Cancer Patients Participating in Early Phase Clinical Trials

Private Payer and Medicare Coverage Policies for Use of Circulating Tumor DNA Tests in Cancer Diagnostics and Treatment

Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies

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