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Observational study on the combination of fruquintinib and standard chemotherapy in the treatment of advanced gastric cancer

Observational study on the combination of fruquintinib and standard chemotherapy in the treatment of advanced gastric cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119681
Enrollment
Unknown
Registered
2026-03-02
Start date
2025-06-01
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Gastric cancer or adenocarcinoma of the gastroesophageal junction

Interventions

Observation group:None

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years old, regardless of gender; 2.Diagnosed by organization and/or cytology as metastatic or locally advanced gastric cancer or gastroesophageal junction adenocarcinoma (Her-2 status is not limited, HER2 positive patients have previously received anti-HER2 treatment); 3.Have experienced at least one progression or failure of systemic therapy; 4.Starting from June 1, 2023, treatment with the combination of fruquintinib and irinotecan or albumin paclitaxel regimen, with at least one tumor assessment after treatment; 5.At least one measurable lesion (RECIST 1.1 standard); 6.ECOG physical condition 0-2 points; 7.Expected survival time >= 12 weeks; 8.Having sufficient organ and bone marrow function; 9.Good compliance and cooperation with follow-up;

Exclusion criteria

Exclusion criteria: 1.Suffering from other primary malignant tumors during the same period, excluding skin basal cell carcinoma, squamous cell carcinoma, or cervical carcinoma in situ after radical surgery; 2.Simultaneously receiving other investigational drugs or approved anti-tumor treatments under development; 3.Drug therapy intervention for less than 2 treatment cycles; 4.Patients who cannot undergo efficacy evaluation and follow-up; 5.Researchers believe that patients who are not suitable for inclusion in this study;

Design outcomes

Primary

MeasureTime frame
Progression-Free Survival;

Secondary

MeasureTime frame
Disease Control Rate;Overall Survival;Objective Response Rate;

Countries

China

Contacts

Public ContactXu Qi

Zhejiang Cancer Hospital

hzxuqi@sina.cn+86 571 8812 2062

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026