[HTML][HTML] Concurrent genetic alterations predict the progression to target therapy in EGFR-mutated advanced NSCLC
Introduction EGFR-mutant NSCLC displays diverse outcomes to tyrosine kinase inhibitor
(TKI) treatment. Because co-occurring genomic alterations might describe different …
(TKI) treatment. Because co-occurring genomic alterations might describe different …
Clinicopathological and prognostic values of telomerase reverse transcriptase (TERT) promoter mutations in ovarian clear cell carcinoma for predicting tumor …
H Yoo, HS Kim - Cancer genomics & proteomics, 2023 - cgp.iiarjournals.org
Background/Aim: A small subset of patients with ovarian clear cell carcinoma (OCCC)
harbors telomerase reverse transcriptase promoter (TERTp) mutations. We aimed to analyze …
harbors telomerase reverse transcriptase promoter (TERTp) mutations. We aimed to analyze …
[HTML][HTML] Clinical application of next-generation sequencing in patients with breast cancer: real-world data
KJ Suh, SH Kim, YJ Kim, H Shin, E Kang… - Journal of Breast …, 2022 - ncbi.nlm.nih.gov
Purpose Next-generation sequencing (NGS)-based tumor panel testing has been
reimbursed by the Korean government since 2017. We evaluated the use of NGS-based …
reimbursed by the Korean government since 2017. We evaluated the use of NGS-based …
[HTML][HTML] Recommendations for the use of next-generation sequencing and the molecular tumor board for patients with advanced cancer: a report from KSMO and …
Next-generation sequencing (NGS) is becoming essential in the fields of precision oncology.
With implementation of NGS in daily clinic, the needs for continued education, facilitated …
With implementation of NGS in daily clinic, the needs for continued education, facilitated …
[HTML][HTML] Actionability evaluation of biliary tract cancer by genome transcriptome analysis and Asian cancer knowledgebase
Introduction: Treatment options for biliary tract cancer (BTC) are very limited. It is necessary
to investigate actionable genes and candidate drugs using a sophisticated knowledgebase …
to investigate actionable genes and candidate drugs using a sophisticated knowledgebase …
Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
JH Kim, S Yoon, DH Lee, SJ Jang, SM Chun… - Cancer …, 2021 - Wiley Online Library
Purpose This study investigated the clinical utility of next‐generation sequencing (NGS) for
detection of genetic alterations and its implications on treatment of lung adenocarcinoma in …
detection of genetic alterations and its implications on treatment of lung adenocarcinoma in …
State legislative trends related to biomarker testing
G Sadigh, HG Goeckner, EA Kazerooni, BE Johnson… - Cancer, 2022 - Wiley Online Library
Comprehensive biomarker testing has become the standard of care for informing the choice
of the most appropriate targeted therapy for many patients with advanced cancer. Despite …
of the most appropriate targeted therapy for many patients with advanced cancer. Despite …
[HTML][HTML] Exploring the DNA methylome of Korean patients with colorectal cancer consolidates the clinical implications of cancer-associated methylation markers
Aberrant DNA methylation plays a critical role in the development and progression of
colorectal cancer (CRC), which has high incidence and mortality rates in Korea. Various …
colorectal cancer (CRC), which has high incidence and mortality rates in Korea. Various …
Simple prediction model for homologous recombination deficiency in breast cancers in adolescents and young adults
T Watanabe, T Honda, H Totsuka, M Yoshida… - Breast Cancer Research …, 2020 - Springer
Purpose Homologous recombination deficiency (HRD), which influences the efficacy of
PARP inhibitor-and platinum agent-based therapies, is a prevalent phenotype of breast …
PARP inhibitor-and platinum agent-based therapies, is a prevalent phenotype of breast …
Evaluation of false positive and false negative errors in targeted next generation sequencing
Y Moon, YH Kim, JK Kim, CH Hong, EK Kang, HW Choi… - bioRxiv, 2024 - biorxiv.org
Background: Although next generation sequencing (NGS) has been adopted as an essential
diagnostic tool in various diseases, NGS errors have been the most serious problem in …
diagnostic tool in various diseases, NGS errors have been the most serious problem in …