A Clinical Trial With Apatinib for Subjects With Refractory Malignant Ascites

NCT ID: NCT03020979

Last Updated: 2017-05-31

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-01-31
• Study Completion Date: 2019-12-31

Brief Summary

Malignant ascites is a severe complication of many types of human cancer. Animal and clinical analyses have shown that angiogenesis plays a critical role in the formation of malignant ascites. Therefore, drugs such as apatinib that target angiogenesis may control the development of malignant ascites. The study is to evaluate the efficacy and safety of apatinib in patients with refractory malignant ascites.

Detailed Description

The study is to investigate the efficacy and safety of apatinib in patients with refractory malignant ascites. A total of 120 patients with performance status 0-2 were enrolled in this study and 500mg apatinib tablets were administered orally, once daily until disease progression or intolerable toxicity or patients withdrawal of consent.

Conditions

Malignant Ascites; Apatinib

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

500mg apatinib

Patients will receive 500mg of apatinib tablet orally, once daily.

Group Type: EXPERIMENTAL

Apatinib

Intervention Type: DRUG

Patients will take 500mg apatinib daily orally.

Interventions

Apatinib

Patients will take 500mg apatinib daily orally.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Persistent or symptomatic ascites with positive cytology secondary to any histologically confirmed tumor type not amenable to cytoreductive surgery or additional chemotherapy
• Patients may enroll in this study irrespective of previous therapy including diuretics, surgery, chemotherapy, immunotherapy and radiation therapy
• Must have received a minimum of two paracentesis procedures and a trial of diuretic therapy within 60 days of study entry
• Age Restrictions: 18-75 years
• Life Expectancy: 12 weeks or more
• ECOG Performance Status: 0-2
• Able and willing to provide informed consent and comply with study and/or follow-up procedures
• Normal organ and marrow function as defined by: Leukocytes >/= 3,000/mcL; Absolute neutrophil count >/= 1,500/mcL; Platelets >/= 100,000/mcL; Total bilirubin within normal institutional limits; AST (SGOT)/ALT(SGPT) </= 2.5 X institutional upper limit of normal (ULN); Creatinine within normal institutional limits OR Creatinine clearance >/+ 60 mL/min for patients with creatinine levels above the institutional normal; Serum Potassium within normal institutional limits; Serum Sodium within normal institutional limits

Exclusion Criteria

• Patients having received anti-angiogenic agents as part of the treatment of their malignancy within 60 days prior to study entry
• Current, recent (within 30 days of the first infusion of this study) or planned administration of chemotherapy (including all routes of administration), immunotherapy, biologic therapy, radiation therapy or any other anti-angiogenic therapy (e.g., bevacizumab, other tyrosine kinase inhibitors)
• Current, recent (within 30 days of the first infusion of this study), or planned participation in any other experimental drug study
• Pregnant women; A serum pregnancy test will be given to females of childbearing potential prior to study enrollment and the participant must agree to use adequate contraception (barrier or hormonal methods) prior to study entry and for the duration of study participation.
• Un-controlled hypertension (defined as systolic blood pressure > 140 mmHg and/or diastolic blood pressure > 90 mmHg
• History of hypertensive crisis or hypertensive encephalopathy
• New York Heart Association (NYHA) Grade III or greater congestive heart failure
• History of myocardial infarction, unstable angina, stroke or transient ischemic attack within 6 months prior to study entry
• Known CNS disease, except for treated brain metastasis.
• Significant vascular disease (e.g., aortic aneurysm, requiring surgical repair or recent peripheral arterial thrombosis) within 6 months prior to study entry
• History of gastrointestinal hemorrhage within 6 month prior to study entry
• Evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation)
• Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to study entry or anticipation of need for major surgical procedure during the course of the study
• Core biopsy or other minor surgical procedure, excluding placement of a vascular access device or paracentesis/thoracentesis, within 7 days prior to study entry
• History of abdominal fistula or gastrointestinal perforation within 6 months prior to study entry
• Any bowel obstruction that has not fully recovered despite medical or surgical intervention prior to study entry
• Evidence of bowel wall thickening outside the site of the known primary malignancy on baseline radiographs
• Serious, non-healing wound, active ulcer, or untreated bone fracture
• Proteinuria as demonstrated by a Urine Protein/Creatinine ration >/= 1.0 at screening
• Known hypersensitivity to any component of apatinib.

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

Sponsors

The First Affiliated Hospital of Bengbu Medical University

OTHER

Sponsor Role: lead

Responsible Party

Qiong Wu

M.D. Ph.D.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Qiong Wu

Bengbu, Anhui, China

Site Status: RECRUITING

Countries

China

Central Contacts

Qiong Wu, M.D. Ph.D.

Role: CONTACT

byzlnk@163.com

+86-552-3074480

Facility Contacts

Rui Wang, MD

Role: primary

byzlnk@163.com

+86-0552-3074480

Other Identifiers

BYEC20161201

Identifier Type: -

Identifier Source: org_study_id