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RecruitingNCT07551440Updated Apr 24, 2026

Identification of Therapeutic Targets in Metastatic Gastric Cancer

An observational study in Stomach Neoplasms, Benign, sponsored by Chinese University of Hong Kong. Recruiting at 1 site in Hong Kong. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-04-24.

Sponsored by Chinese University of Hong Kong · Observational

From the registry’s dates

  • Started Oct 2023; still recruiting 2 years 11 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 80 Years
Sex
All
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Study summary

This is a pilot study aiming at identifying novel therapeutic molecular targets in patients with gastric cancer with lymph nodes or distant metastasis. All patients who are diagnosed with gastric cancer with metastases in the Prince of Wales Hospital will be screened for eligibility.

02

Conditions studied

  • Stomach Neoplasms, Benign

Keywords

  • gastric cancer, metastatic, therapeutic targets
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In context

Stomach Neoplasms

2,851 studies on the registry are indexed under Stomach Neoplasms; 864 are open to participants now.

This study's planned enrollment of 100 is below the median of 274 across 670 observational studies indexed under Stomach Neoplasms.

Browse Stomach Neoplasms studies →

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients admitted into PWH

Inclusion criteria

  1. Patients age >= 18, \<= 80 years old
  2. Performance status (WHO) \<=2
  3. Gastric adenocarcinoma with lymph node metastasis or distant metastasis such as liver metastases, lung metastases, bone metastases, peritoneum metastases
  4. Patients with isolated ovarian metastasis could be included
  5. Patients who will be undergoing neoadjuvant chemotherapy/ target therapy/ immunotherapy or palliative chemotherapy/ target therapy/ immunotherapy
  6. Ability to give written consent before the commencement of treatment

Exclusion criteria

Exclusion Criteria:

  1. Patient who will not be undergoing neoadjuvant chemotherapy/ target therapy/ immunotherapy or palliative chemotherapy/ target therapy/ immunotherapy
  2. Pregnancy or breastfeeding
  3. Patients with irreversible coagulation disorders
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Biobank construction

    Recruit patients and collect the required biological samples (i.e. tumor tissues, blood and ascites samples) for biobank construction.

    Time frame: Collect at baseline(pre-treatment) and/or during interval surgery if clinically indicated and/or after completing all systemic and surgical treatment if patient required an endoscopy or laparoscopy due to clinical need only.

  2. Detection of noval therapeutic targets for treating gastric cancer cancer with metastases.

    Biological samples (i.e. tissue, blood and ascites samples) collected from enrolled patients will be used in genome and transcriptome analysis using next generation sequencing, DNA mutation detection using digital PCR and mass spectrometry-based proteomic.

    Time frame: Collect at baseline(pre-treatment) and/or during interval surgery if clinically indicated and/or after completing all systemic and surgical treatment if patient required an endoscopy or laparoscopy due to clinical need only.

  3. Organoid culture for drug sensitivity assay

    Gastric tumor tissues are collected from enrolled patients to establish patient-derived organoids and subject to drug sensitivity assay. The choice of drugs will depend on the molecular analysis results and will be advised by oncologists.

    Time frame: Collect at baseline(pre-treatment) and/or during interval surgery if clinically indicated and/or after completing all systemic and surgical treatment if patient required an endoscopy or laparoscopy due to clinical need only.

Secondary outcomes

  1. Clinical Outcome - Overall survival

    Patients' overall survival will also be recorded.

    Time frame: through study completion, an average of 5 year

  2. Clinical Outcome - Progression-free survival

    Patients' progression-free survival will also be recorded.

    Time frame: through study completion, an average of 5 year

  3. Clinical Outcome - Karnofsky Score

    Karnofsky Score for measuring quality of life will be recorded

    Time frame: At baseline measurement

  4. Clinical Outcome - Time point of metastasis

    Patients' time point of metastasis, whether it is synchronous or metachronous will be recorded

    Time frame: Recruitment till death or 5 year

  5. Clinical Outcome - Number of previous chemotherapy/ target therapy/ immunotherapy

    Number of previous chemotherapy/ target therapy/ immunotherapy received by the patients will be recorded

    Time frame: Measured and asked at baseline

  6. Clinical Outcome - Presence of ascites

    Presence of ascites on recruited patients will be recorded

    Time frame: Recruitment till death or 5 year

  7. Clinical Outcome - Cancer Restaging

    Stage of cancer will be recorded and determined with CT/PETCT scan

    Time frame: Post-treatment till death or 5 year

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Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07551440
Lead sponsor
Chinese University of Hong Kong
Responsible party
CHAN SHANNON MELISSA (Assistant Professor, Chinese University of Hong Kong) — Principal investigator
First posted
Apr 24, 2026
Start date
Oct 15, 2023
Primary completion
Apr 2033 (estimated)
Completion
Oct 2033 (estimated)
Last update
Apr 24, 2026

Study contacts

Shannon Melissa Chan, PhD
Contact
shannonchan@surgery.cuhk.edu.hk
35052627

Oversight

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

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