Gastric cancer

E Van Cutsem, X Sagaert, B Topal, K Haustermans… - The Lancet, 2016 - thelancet.com
Gastric cancer is one of the leading causes of cancer-related death worldwide. Many
patients have inoperable disease at diagnosis or have recurrent disease after resection with …

Gastric cancer: descriptive epidemiology, risk factors, screening, and prevention

P Karimi, F Islami, S Anandasabapathy… - … , biomarkers & prevention, 2014 - AACR
Less than a century ago, gastric cancer was the most common cancer in the United States
and perhaps throughout the world. Despite its worldwide decline in incidence over the past …

NCCN guidelines insights: genetic/familial high-risk assessment: breast and ovarian, version 2.2017

MB Daly, R Pilarski, M Berry, SS Buys… - Journal of the National …, 2017 - jnccn.org
The NCCN Clinical Practice Guidelines in Oncology for Genetic/Familial High-Risk
Assessment: Breast and Ovarian provide recommendations for genetic testing and …

A study of over 35,000 women with breast cancer tested with a 25‐gene panel of hereditary cancer genes

SS Buys, JF Sandbach, A Gammon, G Patel, J Kidd… - Cancer, 2017 - Wiley Online Library
BACKGROUND As panel testing becomes more common in clinical practice, it is important
to understand the prevalence and trends associated with the pathogenic variants (PVs) …

Hereditary diffuse gastric cancer syndrome: CDH1 mutations and beyond

S Hansford, P Kaurah, H Li-Chang, M Woo… - JAMA …, 2015 - jamanetwork.com
Importance E-cadherin (CDH1) is a cancer predisposition gene mutated in families meeting
clinically defined hereditary diffuse gastric cancer (HDGC). Reliable estimates of cancer risk …

Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel

N Tung, C Battelli, B Allen, R Kaldate, S Bhatnagar… - Cancer, 2015 - Wiley Online Library
BACKGROUND Next‐generation sequencing (NGS) allows for simultaneous sequencing of
multiple cancer susceptibility genes and, for an individual, may be more efficient and less …

Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment

AW Kurian, EE Hare, MA Mills, KE Kingham… - Journal of clinical …, 2014 - ascopubs.org
Purpose Multiple-gene sequencing is entering practice, but its clinical value is unknown. We
evaluated the performance of a customized germline-DNA sequencing panel for cancer-risk …

[HTML][HTML] Cell-free DNA: hope and potential application in cancer

Y Yan, Q Guo, F Wang, R Adhikari, Z Zhu… - Frontiers in cell and …, 2021 - frontiersin.org
Cell-free DNA (cfDNA) is easily accessible in peripheral blood and can be used as
biomarkers for cancer diagnostics, prognostics, and therapeutics. The applications of cfDNA …

Hereditary breast cancer: the era of new susceptibility genes

P Apostolou, F Fostira - BioMed research international, 2013 - Wiley Online Library
Breast cancer is the most common malignancy among females. 5%–10% of breast cancer
cases are hereditary and are caused by pathogenic mutations in the considered reference …

Gastric cancer: emerging trends in prevention, diagnosis, and treatment

DA Norwood, E Montalvan-Sanchez… - Gastroenterology …, 2022 - gastro.theclinics.com
Gastric adenocarcinoma (GC) is the third leading cause of global cancer mortality, and the
leading infection-associated cancer with more than 1 million incident cases annually and …