Apatinib Combined With Capecitabine Compared With Apatinib Treat Advanced Hepatocellular Carcinoma

NCT ID: NCT03114085

Last Updated: 2017-05-15

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 170 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-05-20
• Study Completion Date: 2019-05-20

Brief Summary

It is an open,randomized,controlled study, and the purpose of this study is to observe and evaluate the efficacy and safety of Apatinib combined with Capecitabine in the treatment of patients with advanced hepatocellular carcinoma.

Detailed Description

This study is the clinical study of Apatinib combined with Capecitabine compared with Apatinib in the treatment of advanced non-resectable Hepatocellular Carcinoma, the object is patients with advanced hepatocellular carcinoma,its purpose is to observe and evaluate the efficacy and safety of Apatinib Mesylate Tablets combined with Capecitabine in the treatment of patients with advanced hepatocellular carcinoma, its main primary endpoint is TTP (time to progression) while the secondary endpoint is OS (overall survival), ORR (objective response rate), DCR (disease control rate), serum alpha-fetoprotein (AFP) levels and quality of life. 170 patients will be enrolled and 1:1 randomized into two groups: Apatinib combined Capecitabine and Apatinib alone. Major safety indicators are Vital signs, laboratory indicators, adverse events (AE), serious adverse events (SAE), drug-related AE and SAE, and specific AE (such as hypertension, proteinuria, and hand-foot syndrome), according to NCI-CTCAE.

Conditions

Hepatocellular Carcinoma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Apatinib Combined with Capecitabine

Apatinib,500mg,once a day, orally (after breakfast),from day 1 to day 21 (including day 21) for continuous administration, every 21 days for one cycle. If after two dose adjustments, the subject still can not tolerate toxicity, he or she should be out of group; Capecitabine,1000mg/m2,twice a day (at intervals of 12 hours,equivalent to a total daily dose of 2000 mg / m2),orally,sustained 14 days, off for 7 days, every 21 days for a cycle. If after two dose adjustments, the subject still can not tolerate toxicity, he or she should be out of group.

Group Type: EXPERIMENTAL

Capecitabine

Intervention Type: DRUG

Capecitabine 1000mg/m2 po bid, d1-d14, every 21 days for a cycle;

Apatinib

Intervention Type: DRUG

Apatinib 500 mg po qd, d1-d21, every 21 days for one cycle

Apatinib

Apatinib,500mg,once a day, orally (after breakfast),from day 1 to day 21 (including day 21) for continuous administration, every 21 days for one cycle. If after two dose adjustments, the subject still can not tolerate toxicity, he or she should be out of group;

Group Type: ACTIVE_COMPARATOR

Apatinib

Intervention Type: DRUG

Apatinib 500 mg po qd, d1-d21, every 21 days for one cycle

Interventions

Capecitabine

Capecitabine 1000mg/m2 po bid, d1-d14, every 21 days for a cycle;

Intervention Type: DRUG

Apatinib

Apatinib 500 mg po qd, d1-d21, every 21 days for one cycle

Intervention Type: DRUG

Other Intervention Names

Aibin; Aitan

Eligibility Criteria

Inclusion Criteria

• Age: ≥18-75 years old
• Recurrent / Metastatic non-resectable HCC patients who are in strict compliance with clinical diagnostic criteria of the Standard of Primary Liver Cancer Diagnosis and Treatment (2011 edition) or diagnosis by histopathology or cytology, and are unable to accept palliative surgery or radiotherapy, and have at least one measurable lesion (according to mRECIST, the measurable lesions spiral CT scan length ≥ 10mm or enlarged lymph node diameter ≥ 15mm); the largest tumor ≤ 10cm
• Child-Pugh liver function rating: A or better B (≤ 7 points)
• BCLC stage is B-C period
• ECOG PS score within 1 week before enrollment: 0-1 points
• Expected survival time ≥12 weeks
• The main organs function is normal, that is, meeting the following criteria:

Blood examination:

HB ≥ 90 g / L; ANC ≥ 1.5 × 109 / L; PLT ≥ 60 × 109 / L;

Biochemical examination:

ALB ≥ 29 g / L; ALT and AST < 2.5 ULN; TBIL ≤ 2ULN; Creatinine ≤ 1.5ULN; (Albumin and bilirubin two indicators can only have one for 2 points in Child-Pugh rating)

• Women of childbearing age shall undergo pregnancy tests within 7 days before enrollment
• People to be tested are volunteered to join the study and sign informed consent. They should have good compliance and are easy to follow-up

Exclusion Criteria

• Patients with hepatic cholangiocarcinoma or mixed cell carcinoma or fibrous lamellar cell carcinoma; or at the same time with other untreated malignant tumors in the past (within 5 years), except for cured skin basal cell carcinoma and cervical carcinoma in situ
• Patients who are preparing for liver transplantation (except those who have undergone liver transplantation)
• Patients with high blood pressure, and it can't be reduced to normal range (systolic blood pressure> 140 mmHg, diastolic blood pressure> 90 mmHg) by antihypertensive drug therapy
• Patients with level two or above myocardial ischemia or myocardial infarction, or poor controlled arrhythmia (including QTc interval men ≥ 450 ms, female ≥ 470 ms)
• According to NYHA standard Ⅲ ~ Ⅳ grade cardiac insufficiency or cardiac color Doppler ultrasound examination: LVEF (left ventricular ejection fraction) <50%
• Have a variety of factors affecting oral drugs (such as can not swallow, chronic diarrhea and intestinal obstruction, significantly affect drug taking and absorption)
• There is a history of gastrointestinal bleeding or a clear tendency to gastrointestinal bleeding in the past 6 months, such as: esophageal varicose veins with bleeding risk, local active ulcer lesions. Fecal occult blood ≥ (++) can not be grouped, if fecal occult blood (+),endoscopy is required
• Abdominal fistula, gastrointestinal perforation or abdominal abscess appeared within 28 days of participating in the study
• Coagulation dysfunction (INR> 1.5 or prothrombin time (PT)> ULN + 4 seconds), with bleeding tendency or are receiving thrombolytic or anticoagulant therapy
• Patients with central nervous system metastasis or brain metastases
• Patients who is suffering or had suffered pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, radiation pneumonia, drug-related pneumonia, or severe impairment of lung function
• Urine test indicated urine protein ≥ ++ or confirmed 24 hours urine protein> 1.0 g
• A strong CYP3A4 inhibitor treatment was received within 7 days before the study, or a strong CYP3A4 inducer was received within 12 days before the study
• Pregnant or lactating women; fertility patients who are reluctant or unable to take effective contraceptive measures
• Patients with mental illness, or history of mental drug abuse
• Patients with bone metastases had received palliative radiotherapy (radiotherapy area> 5% bone marrow area) within 4 weeks before participating in the study
• Patients who are joint with HIV infection

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

First Affiliated Hospital of Guangxi Medical University

OTHER

Sponsor Role: lead

Responsible Party

Zeng Zhiming

Doctor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Zhiming Zeng, Master

Role: PRINCIPAL_INVESTIGATOR

Guangxi Medical University First Affiliated Hospital

Central Contacts

Zhiming Zeng, Master

Role: CONTACT

zengzhiming031317@163.com

8618677081832

Other Identifiers

HRGX-001

Identifier Type: -

Identifier Source: org_study_id