Apatinib for Advanced Biliary Carcinoma

Phase 2

• Conditions: Biliary Tract Neoplasms
• Interventions: Drug: Apatinib

• Registration Number: NCT03427242
• Lead Sponsor: Fudan University

Brief Summary

This is a phase II open-label, one-arm, single-center study of apatinib for eligible patients with advanced biliary tract carcinoma after the first-line treatment failure. A total of 55 patients is planned for enrollment. The time for enrollment is from Nov 2017 to Nov 2020, the the follow-up will be ended after Nov 2021. Patients in the study would receive oral apatinib 500-750mg qd until progression of disease.

Detailed Description

Not available

Study Timeline

• Status Verified: 2017-11
• Study Start: 2017-11-01
• Study First Submitted: 2018-01-25
• Study First Submitted QC: 2018-02-02
• Last Update Submitted: 2018-02-02
• Study First Posted: 2018-02-09
• Last Update Posted: 2018-02-09
• Primary Completion: 2021-10-31
• Study Completion: 2022-10-31

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 55

Inclusion Criteria

1. Patients age between 18 and 70 years
2. Histologically confirmed advanced biliary tract carcinoma (BTC) or metastatic BTC
3. Prior lack of response or intolerance to at least one chemotherapeutic regimens (including gemcitabine).
4. At least one measurable lesion as defined by RECIST 1.1
5. An Eastern Cooperative Oncology Group performance status of 0 to 2
6. Life expectancy ≥ 12 weeks
7. For those who received other anti-tumor treatment, the damage should have been restored, with the time interval from last dose of nitroso or mitomycin≥6 weeks and interval from last dose of other cytotoxic drugs, radiation or surgery (the wound should be healed completely) ≥4 weeks.
8. Acceptable hematologic, hepatic, and renal function within 7 days from screening： the blood ANC count≥1.5x109 /L; hemoglobin ≥ 9.0 g/dl，the blood platelet count≥80 x109 /L, total bilirubin < 1.5 x ULN, ALT and AST< 2.5 x ULN(< 5 x ULN for patients with live metastasis), serum creatinine≤1 x ULN，endogenous creatinine clearance rate >50ml/min
9. Women of reproductive age need to take effective contraceptive measures

Exclusion Criteria

1. With other malignant tumor in 5 years，except for cured cervical carcinoma in situ or basal cell carcinoma.
2. Uncontrolled blood pressure on medication (140/90 mmHg); patients with > Grade 1 coronary heart disease, cardiac arrhythmias or cardiac dysfunction
3. Symptomatic brain or meningeal metastasis
4. History of uncontrolled seizures, central nervous system dysfunction or mental disorder
5. Uncontrolled pleural or peritoneal effusion
6. Undergoing dialysis
7. Severe or uncontrolled infection
8. With multiple factors that affecting oral administration
9. Abnormal coagulation function or those receiving thrombolytics or anticoagulants
10. Patients with tendency of gastrointestinal hemorrhage, including active peptic ulcer with fecal occult blood ++, hematemesis or melena within 3 months
11. Participation in other drug clinical trials within 4 weeks
12. Weight below 40kg
13. urine protein ≥2+

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
treatment arm	Apatinib	oral apatinib

Primary Outcome Measures

Name	Time	Method
PFS	from the time signing of ICF until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months	progression free survival

Secondary Outcome Measures

Name	Time	Method
OS	from the time signing of ICF until the date of death from any cause, assessed up to 48 months	overall survival

Trial Locations

Locations (1)

Fudan University Shanghai Cancer Center; 🇨🇳 Shanghai, Shanghai, China