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Impact of MET Gene Abnormalities on the Efficacy of Anti-HER2 Targeted Therapy in Chinese Gastric Cancer Patients: A Multicenter, Retrospective Cohort Study

Impact of MET Gene Abnormalities on the Efficacy of Anti-HER2 Targeted Therapy in Chinese Gastric Cancer Patients: A Multicenter, Retrospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117225
Enrollment
Unknown
Registered
2026-01-21
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric cancer

Interventions

Observation group for gastric cancer treatment:None

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age >= 18 years old; (2) Locally advanced or metastatic gastric or gastroesophageal junction epithelial malignancies that are not resectable, confirmed by histological or cytological examination; (3) Tumor tissue HER2 expression is confirmed by immunohistochemical staining (immunohistochemistry, IHC) as HER2 >= 1+, and/or positive by fluorescence in situ hybridization technique (fluorescence in situ hybridization, FISH); (4) Received HER2-targeted therapy from June 1, 2016 to May 31, 2023; (5) Has follow-up information.

Exclusion criteria

Exclusion criteria: 1. Suffering from other malignant tumors simultaneously; 2. No tumor assessment was conducted after HER2-targeted treatment; 3. Incomplete clinical and pathological data (including but not limited to the absence of previous treatment information, tumor assessment information after anti-HER2 treatment, etc.); 4. Patients who received radiotherapy for target lesions during HER2-targeted treatment; 5. Other situations that the researchers consider not suitable for inclusion in the analysis, such as inconsistent tumor assessment information before and after, which may affect the assessment of the study endpoint.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Progression-free survival period;

Countries

China

Contacts

Public ContactXiaoxiao Ge

Shanghai East Hospital

tinagxx.zs@163.com+86 21 3880 4518

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026