Skip to content

A phase II, single arm study for apatinib combined with tegafur maintenance therapy for advanced gastric cancer and gastroesophageal junction cancer

A phase II, single arm study for apatinib combined with tegafur maintenance therapy for advanced gastric cancer and gastroesophageal junction cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020061
Enrollment
Unknown
Registered
2018-12-12
Start date
2019-01-01
Completion date
Unknown
Last updated
2018-12-18

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

Conditions

gastric cancer

Interventions

Case series:Apatinib mesylate combined with tegafur

Sponsors

Baotou Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 30 patients with advanced ovarian cancer diagnosed by pathology in our hospital from December 2017 to December 2018, aged over 18 years.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women; 2. Participated in other drug clinical trials within 4 weeks before the start of the study. 3. Symptomatic brain/meningeal metastases and simple bone metastases; 4. Patients with hypertension who could not be well controlled by single antihypertensive drugs (systolic pressure > 140 mmHg, diastolic pressure > 90 mmHg), myocardial ischemia or myocardial infarction above grade I, arrhythmia above grade I (including QT interval > 440 ms) or cardiac insufficiency; 5. There are many factors affecting the oral and absorption of drugs (such as inability to swallow, Post-gastrointestinal resection, chronic diarrhea and intestinal obstruction, etc.); 6. The coagulation function is abnormal and is undergoing thrombolysis or anticoagulation therapy, which is prone to bleeding; 7. There are clear concerns about gastrointestinal bleeding (e.g. local active ulcer lesions, positive stool occult blood); 8. Arteriovenous thrombosis events occurred within 6 months before the start of the study, such as cerebrovascular accident (including temporary ischemic attack), deep venous thrombosis and pulmonary embolism; 9. Wounds or fractures in the chest and other parts that have not been healed for a long time; 10. Urinary routine indicated that urinary protein (++) and confirmed 24-hour urinary protein quantification > 1.0 G. 11. Severe or uncontrolled infections exist; 12. Mental illness or other conditions affecting patient compliance; 13. Patients with past and present objective evidence of pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, radiation pneumonia, drug-related pneumonia, severe impairment of lung function, etc. Other malignant tumors have been reported in the past five years, except for cured basal cell carcinoma of skin and carcinoma in situ of cervix.

Design outcomes

Primary

MeasureTime frame
PFS;ORR;DCR;

Secondary

MeasureTime frame
Safety;OS;

Countries

China

Contacts

Public ContactHua Yunqi

Baotou Cancer Hospital

592676401@qq.com+86 13015056119

Outcome results

None listed

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