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One-arm, single-center, open-label clinical study of concurrent chemoradiotherapy combined with adjuvant chemotherapy and antiangiogenic therapy for advanced malignant tumors

One-arm, single-center, open-label clinical study of concurrent chemoradiotherapy combined with adjuvant chemotherapy and antiangiogenic therapy for advanced malignant tumors

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017537
Enrollment
Unknown
Registered
2018-08-02
Start date
2018-08-23
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

advanced malignant solid tumors

Interventions

Sponsors

Chongqing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old male and female; 2. The expected survival period is =3 months; 3. Advanced malignant solid tumors confirmed by histopathology; 4. ECOG PS: 0-2 points; 5. Bone marrow, liver and kidney function are normal; 6. Subjects voluntarily participated in this study, signed informed consent, followed up with good compliance.

Exclusion criteria

Exclusion criteria: 1. Coagulation dysfunction, bleeding tendency (APTT greater than 1.5ULN or INR > 1.5), such as active peptic ulcer, or receiving thrombolysis or anticoagulant therapy; 2. The following severe concomitant diseases may cause greater risk or affect the compliance of the test: (1) Grade 2 hypertension with uncontrollable drug; (2) Grade III-IV cardiac insufficiency; (3) severe arrhythmia; (4) severe liver and kidney dysfunction; (5) urinary protein = ++, 24 hours Urine protein>1.0g; (6) chronic hepatitis; (7) mental illness; 3. Other anti-VEGF/VEGFR targeted drugs have been used before; 4. Patients who have undergone major surgery and have not healed in the past month; 5. Women during pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
progression-free survival;

Secondary

MeasureTime frame
Overall survival;Disease control rate;Objective remission rate;Quality of Life;

Countries

China

Contacts

Public ContactYing Wang

Chongqing Cancer Hospital

742676160@qq.com+86 13023309167

Outcome results

None listed

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