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RecruitingNCT06550063HERAUpdated Aug 13, 2024

HER2 Status in Esophagogastric Adenocarcinoma and Its Associations With Patient's Clinicopathological Outcomes

An observational study in Esophagus Cancer, Gastric Cancer and HER2-positive Cancer, sponsored by St. James's Hospital, Ireland. Recruiting at 1 site in Ireland. Per ClinicalTrials.gov, last updated 2024-08-13.

Sponsored by St. James's Hospital, Ireland · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
2,188
Sex
All
01

Study summary

Targeted therapies offer promise to improve oncologic outcomes in esophagogastric adenocarcinoma (EGA). The landmark 'Trastuzumab for gastric cancer (ToGA)' trial established the therapeutic value of Human Epidermal Growth Factor Receptor 2 (HER2) directed therapy in advanced gastric and esophagogastric junction adenocarcinoma, setting a standard of care. Further studies, such as DESTINY-gastric01 and DESTINY-gastric02, have demonstrated the efficacy of antibody-drug conjugates (ADCs) targeting HER2-positive gastric and junctional tumours. The use of HER2-directed therapies in the curative intent setting has more recently been evaluated with favourable outcomes in phase II studies. However, data regarding the prevalence and prognostic significance of HER2 overexpression among patients undergoing treatment with curative intent are limited. Furthermore, few studies have evaluated the clinical significance of intratumoural and tumour-metastatic heterogeneity of HER2 expression, and the finding of HER2-low, in this context, which may have important implications for implementation of neoadjuvant targeted therapies in future. While limited single centre series have evaluated the clinicopathologic significance of HER2 status in EGA, no previous international multicentre study of this nature has been reported.

The goal of this international, multi-center, retrospective observational study is to elucidate the prevalence and clinical significance of HER2 expression in patients with EGA across different regions globally. The study also aims to assess the clinical significance of HER2 heterogeneity in a large, international cohort of patients with EGA, and its association with clinicopathological outcomes in patients with advanced and recurrent disease.

02

Conditions studied

  • Esophagus Cancer
  • Gastric Cancer
  • HER2-positive Cancer
  • HER2-low Cancer

Keywords

  • Esophageal cancer
  • Gastric cancer
  • HER2-positive cancer
  • HER2-low cancer
  • Targeted treatment
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

This study is a multi-center, retrospective, international cohort study including a population of patients diagnosed with EGA from 2000 to April 2024 across all stages of disease with primary tumour routinely tested for HER2 status.

Inclusion criteria

  • Patients with newly diagnosed EGA from 2000 to April 2024 across all stages of disease
  • Primary tumour HER2 status tested as routine in all patients with EGA
  • Patients aged 18 years or over

Exclusion criteria

Exclusion Criteria:

  • Patients with esophageal squamous cell carcinoma
04

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
2,188 participants (estimated)
Patient registry
No
05

What researchers measure

Primary outcomes

  1. Geographical variation in HER2 status

    Time frame: 2000 - 2024

Secondary outcomes

  1. Clinical TNM stage

    Time frame: 2000 - 2024

  2. Overall survival

    Time frame: 2000 - 2024

06

Study locations

1 of 1 sites recruiting
  • Trinity St James Cancer Institute
    Dublin, Leinster D08 NHY1, Ireland
    • Nicola B Raftery, MBBCh,MSc · Contact · rafteryn@tcd.ie · +353 86 1675454
    Recruiting
07

Registry details

Key details

Study ID
NCT06550063
Lead sponsor
St. James's Hospital, Ireland
Responsible party
Nicola Raftery (Principal investigator, Dr, St. James's Hospital, Ireland) — Principal investigator
First posted
Aug 12, 2024
Start date
Aug 20, 2024 (estimated)
Primary completion
May 31, 2025 (estimated)
Completion
Aug 31, 2025 (estimated)
Last update
Aug 13, 2024

Study contacts

Nicola B Raftery, MBBCh,MSc
Contact
rafteryn@tcd.ie
+353 86 1675454
John V Reynolds, MBBCh,MD
principal investigator · Trinity St James Cancer Institute

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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