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EGFR mutation detection in ctDNA from NSCLC patient plasma: A cross-platform comparison of leading technologies to support the clinical development of AZD9291

Lung cancer (Amsterdam, Netherlands), 2015-12, Vol.90 (3), p.509-515

2015

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Gefitinib Treatment in EGFR Mutated Caucasian NSCLC: Circulating-Free Tumor DNA as a Surrogate for Determination of EGFR Status

Journal of thoracic oncology, 2014-09, Vol.9 (9), p.1345-1353

2014

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Concordance of BRCA mutation detection in tumor versus blood, and frequency of bi-allelic loss of BRCA in tumors from patients in the phase III SOLO2 trial

Gynecologic oncology, 2021-12, Vol.163 (3), p.563-568

2021

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EGFR Mutation Analysis for Prospective Patient Selection in Two Phase II Registration Studies of Osimertinib

Journal of thoracic oncology, 2017-08, Vol.12 (8), p.1247-1256

2017

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EGFR mutation incidence in non-small-cell lung cancer of adenocarcinoma histology: a systematic review and global map by ethnicity (mutMapII)

American journal of cancer research, 2015-01, Vol.5 (9), p.2892-2911

2015

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EGFR mutation testing in lung cancer: a review of available methods and their use for analysis of tumour tissue and cytology samples

Journal of clinical pathology, 2013-02, Vol.66 (2), p.79-89

2013

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Mutation status concordance between primary lesions and metastatic sites of advanced non-small-cell lung cancer and the impact of mutation testing methodologies: a literature review

Journal of experimental & clinical cancer research, 2015-09, Vol.34 (1), p.92-92, Article 92

2015

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Tissue and Plasma EGFR Mutation Analysis in the FLAURA Trial: Osimertinib versus Comparator EGFR Tyrosine Kinase Inhibitor as First-Line Treatment in Patients with EGFR-Mutated Advanced Non-Small Cell Lung Cancer

Clinical cancer research, 2019-11, Vol.25 (22), p.6644-6652

2019

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Detection of BRCA1, BRCA2, and ATM Alterations in Matched Tumor Tissue and Circulating Tumor DNA in Patients with Prostate Cancer Screened in PROfound

Clinical cancer research, 2023-01, Vol.29 (1), p.81-91

2023

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Open-label, randomized, multicenter, phase 3 study evaluating trastuzumab deruxtecan (T-DXd) as first-line treatment in patients with unresectable, locally advanced, or metastatic non–small cell lung cancer (NSCLC) harboring HER2 exon 19 or 20 mutations (DESTINY-Lung04)

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.TPS9137-TPS9137

2022

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Olaparib Efficacy in Patients with Metastatic Castration-resistant Prostate Cancer and BRCA1, BRCA2, or ATM Alterations Identified by Testing Circulating Tumor DNA

Clinical cancer research, 2023-01, Vol.29 (1), p.92-99

2023

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Concordance of BRCA1 , BRCA2 (BRCA), and ATM mutations identified in matched tumor tissue and circulating tumor DNA (ctDNA) in men with metastatic castration-resistant prostate cancer (mCRPC) screened in the PROfound study

Journal of clinical oncology, 2021-02, Vol.39 (6_suppl), p.26-26

2021

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The landscape of BRCA1 and BRCA2 large rearrangements in an international cohort of over 20000 ovarian tumors identified using next‐generation sequencing

Genes chromosomes & cancer, 2023-10, Vol.62 (10), p.589-596

2023

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Analysis of head and neck carcinoma progression reveals novel and relevant stage-specific changes associated with immortalisation and malignancy

Scientific reports, 2019-08, Vol.9 (1), p.11992-17, Article 11992

2019

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EGFR T790M mutation testing within the osimertinib AURA Phase I study

Lung cancer (Amsterdam, Netherlands), 2017-07, Vol.109, p.9-13

2017

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The landscape of BRCA1 and BRCA2 large rearrangements in an international cohort of over 20 000 ovarian tumors identified using next‐generation sequencing

Genes chromosomes & cancer, 2023-10, Vol.62 (10), p.589-596

2023

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EGFR T790M mutation testing within a phase I study with AZD9291

Journal of clinical oncology, 2014-05, Vol.32 (15_suppl), p.e19051-e19051

2014

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Olaparib efficacy in patients with metastatic castration-resistant prostate cancer (mCRPC) carrying circulating tumor (ct) DNA alterations in BRCA1 , BRCA2 or ATM : Results from the PROfound study

Journal of clinical oncology, 2021-02, Vol.39 (6_suppl), p.27-27

2021

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EN2-2. DESTINY-Lung04 : Trastuzumab deruxtecan as 1L treatment in advanced HER2 exon 19 or 20 mutated NSCLC

Japanese Journal of Lung Cancer, 2022-11, Vol.62 (6), p.560-560

2022

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Analysis of tumor samples from SOLO2: Concordance of BRCA mutation ( BRCA m) detection in tumor vs. blood and frequency of BRCA -specific loss of heterozygosity (LOH) and loss of function somatic mutations

Journal of clinical oncology, 2018-05, Vol.36 (15_suppl), p.12017-12017

2018

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Abstract A8: Mutation mapping in non-small cell lung cancer: A meta-analysis by geography and histology (MutMap)

Clinical cancer research, 2012-02, Vol.18 (3_Supplement), p.A8-A8

2012

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Identification of a Subset of Human Non-Small Cell Lung Cancer Patients with High PI3Kβ and Low PTEN Expression, More Prevalent in Squamous Cell Carcinoma

Clinical cancer research, 2014-02, Vol.20 (3), p.595-603

2014

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Pseudoautosomal linkage of familial hodgkin's lymphoma: molecular analysis of a unique family with leri–weill dyschondrosteosis and hodgkins lymphoma

British journal of haematology, 2003-04, Vol.121 (2), p.377-379

2003

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EGFR mutation detection in ctDNA from NSCLC patient plasma: A cross-platform comparison of technologies to support the clinical development of AZD9291

Journal of clinical oncology, 2014-05, Vol.32 (15_suppl), p.8092-8092

2014

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EGFR mutation detection in ctDNA from NSCLC patient plasma: A cross-platform comparison of leading technologies to support the clinical development of AZD9291

Gefitinib Treatment in EGFR Mutated Caucasian NSCLC: Circulating-Free Tumor DNA as a Surrogate for Determination of EGFR Status

Concordance of BRCA mutation detection in tumor versus blood, and frequency of bi-allelic loss of BRCA in tumors from patients in the phase III SOLO2 trial

EGFR Mutation Analysis for Prospective Patient Selection in Two Phase II Registration Studies of Osimertinib

EGFR mutation incidence in non-small-cell lung cancer of adenocarcinoma histology: a systematic review and global map by ethnicity (mutMapII)

EGFR mutation testing in lung cancer: a review of available methods and their use for analysis of tumour tissue and cytology samples

Mutation status concordance between primary lesions and metastatic sites of advanced non-small-cell lung cancer and the impact of mutation testing methodologies: a literature review

Tissue and Plasma EGFR Mutation Analysis in the FLAURA Trial: Osimertinib versus Comparator EGFR Tyrosine Kinase Inhibitor as First-Line Treatment in Patients with EGFR-Mutated Advanced Non-Small Cell Lung Cancer

Detection of BRCA1, BRCA2, and ATM Alterations in Matched Tumor Tissue and Circulating Tumor DNA in Patients with Prostate Cancer Screened in PROfound

Open-label, randomized, multicenter, phase 3 study evaluating trastuzumab deruxtecan (T-DXd) as first-line treatment in patients with unresectable, locally advanced, or metastatic non–small cell lung cancer (NSCLC) harboring HER2 exon 19 or 20 mutations (DESTINY-Lung04)

Olaparib Efficacy in Patients with Metastatic Castration-resistant Prostate Cancer and BRCA1, BRCA2, or ATM Alterations Identified by Testing Circulating Tumor DNA

Concordance of BRCA1 , BRCA2 (BRCA), and ATM mutations identified in matched tumor tissue and circulating tumor DNA (ctDNA) in men with metastatic castration-resistant prostate cancer (mCRPC) screened in the PROfound study

The landscape of BRCA1 and BRCA2 large rearrangements in an international cohort of over 20000 ovarian tumors identified using next‐generation sequencing

Analysis of head and neck carcinoma progression reveals novel and relevant stage-specific changes associated with immortalisation and malignancy

EGFR T790M mutation testing within the osimertinib AURA Phase I study

The landscape of BRCA1 and BRCA2 large rearrangements in an international cohort of over 20 000 ovarian tumors identified using next‐generation sequencing

EGFR T790M mutation testing within a phase I study with AZD9291

Olaparib efficacy in patients with metastatic castration-resistant prostate cancer (mCRPC) carrying circulating tumor (ct) DNA alterations in BRCA1 , BRCA2 or ATM : Results from the PROfound study

Identifying homologous recombination deficiency in breast cancer: genomic instability score distributions differ among breast cancer subtypes

EN2-2. DESTINY-Lung04 : Trastuzumab deruxtecan as 1L treatment in advanced HER2 exon 19 or 20 mutated NSCLC

Analysis of tumor samples from SOLO2: Concordance of BRCA mutation ( BRCA m) detection in tumor vs. blood and frequency of BRCA -specific loss of heterozygosity (LOH) and loss of function somatic mutations

Abstract A8: Mutation mapping in non-small cell lung cancer: A meta-analysis by geography and histology (MutMap)

Identification of a Subset of Human Non-Small Cell Lung Cancer Patients with High PI3Kβ and Low PTEN Expression, More Prevalent in Squamous Cell Carcinoma

Pseudoautosomal linkage of familial hodgkin's lymphoma: molecular analysis of a unique family with leri–weill dyschondrosteosis and hodgkins lymphoma

EGFR mutation detection in ctDNA from NSCLC patient plasma: A cross-platform comparison of technologies to support the clinical development of AZD9291

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