Chilean Gastric Cancer Task Force (FORCE 1)

NCT03158571 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 116

Last updated 2019-06-17

No results posted yet for this study

Summary

Background. Gastric cancer (GC) is the world's second leading cause of neoplastic mortality. Genetic alterations, response to treatments and mortality rates are highly heterogeneous across different regions. In Chile, GC is the leading cause of cancer death, affecting 20 per 100,000 people and \>3,000 deaths/year. Clinical outcomes and response to "one size fits all" therapies are highly heterogeneous and thus a better stratification of patients may aid cancer treatment and response.

Study design/methods. The Gastric Cancer Task Force (GCTF) is a Chilean collaborative, non-interventional retrospective study that seeks to stratify gastric adenocarcinomas (GACs) using retrospect clinical outcomes and genomic, epigenomic and protein alterations in a cohort of 200 patients. Tumor samples from the pathology department and the Cancer Center at UC Christus healthcare network at Pontificia Universidad Católica de Chile will be analyzed using a panel of 143 known cancer genes (Oncomine Comprehensive Assay) at the Center of Excellence of Precision Medicine (CEMP) in Santiago, Chile. Additionally, gene promoter methylation will be performed and selected clinically relevant proteins (e.g. PD-L1, Erb-2, VEGFR2 among others) will be assessed by Tissue Microarray, Epstein-Barr virus (EBV) status will also be assessed. Observations will be correlated to 120 clinical parameters, including general patient information, cancer history, laboratory studies, comorbidity index, chemotherapy, targeted therapies, efficacy and follow-up.

Discussion. The development of a clinically meaningful classification that encompasses comprehensive clinical and molecular parameters may improve patient treatment, predict clinical outcomes, aid patient selection for clinical trials and offer insights into future preventive and/or therapeutic strategies.

Conditions

  • Biomarkers

Sponsors & Collaborators

  • Center of Excellence of Precision Medicine (CEMP)

    collaborator UNKNOWN
  • Advanced Center for Chronic Diseases (ACCDiS)

    collaborator UNKNOWN
  • Millennium Institute on Immunology and Immunotherapy

    collaborator OTHER
  • Center UC for Investigation in Oncology (CITO)

    collaborator UNKNOWN
  • Centre of Clinical Research, Health Technology Assessment Unit

    collaborator UNKNOWN
  • National Scientific and Technical Research Council (CONICET), Argentina

    collaborator UNKNOWN
  • Grupo Oncologico Cooperativo del Sur (GOCS), Argentina

    collaborator UNKNOWN
  • Hospital Universitario central de Asurias, Oviedo, España

    collaborator UNKNOWN
  • Hospital Morales Meseger, Murcia, España

    collaborator UNKNOWN
  • Centro de Cancer. Pontificia Universidad Católica de Chile

    collaborator UNKNOWN
  • Hematology and Oncology Department

    collaborator UNKNOWN
  • Pontificia Universidad Catolica de Chile

    lead OTHER

Principal Investigators

  • Marcelo Garrido, MD · Pontificia Universidad Catolica de Chile

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-01
Primary Completion
2018-04-30
Completion
2019-01-01

Countries

  • Chile

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03158571 on ClinicalTrials.gov