Apatinib, Esophageal Cancer, Metastatic Esophageal Cancer
Conditions
Keywords
Esophageal cancer, Metastatic esophageal cancer, Apatinib
Brief summary
Patients with esophageal cancer that had metastatic lesions after been treated with surgery or definitive chemoradiotherapy are being asked to participate in this study. Apatinib is a small-molecule vascular endothelial growth factors receptor (VEGFR) tyrosine kinase inhibitor, similar to vatalanib (PTK787), but with a binding affinity 10 times that of vatalanib or sorafenib. The purpose of this study is to determine what effects apatinib has on metastatic esophageal cancer. These effects include whether apatinib could shrink the tumor or slow down its growth and what side effects apatinib will have on the tumor.
Detailed description
The purpose of this study is to determine what effects apatinib has on metastatic esophageal cancer patients after been treated with surgery or definitive chemoradiotherapy. These effects include whether apatinib could shrink the tumor or slow down its growth and what side effects apatinib will have on the tumor. Eligible are patients with metastatic esophageal cancer who have achieved stable disease or have disease progression after systemic therapy (surgery or definitive chemoradiotherapy) and have at least one separate measurable sites of metastatic lesions. Extent of metastatic disease is recorded either at CT or MRI scanning. Apatinib (850mg) is given daily during the therapy for 28 days. Tumor response is evaluated by assessing clinical and CT/MRI response in the metastatic sites. A Phase II clinical trial based on an optimum two-stage Phase II Simon design is used to conduct this pilot study. Ten patients will be treated in Stage one; if there are no tumor responses, the trial will be terminated. If there are one or more responses in Stage One, the trial will proceed to enroll an additional 19 patients.
Interventions
DRUGApatinib
Patients with metastatic lesions of esophageal cancer after been treated with surgery or definitive chemoradiotherapy receiving Apatinib (850mg) daily over 4 weeks.
Sponsors
Hangzhou Cancer Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patients with histologically confirmed esophageal cancer which is persistent and metastatic or recurrent and metastatic; 2. Patients must have distinct measurable metastatic sites at least 1 cm of larger in their largest diameter; 3. Age ≥18 years; 4. Metastatic disease measurable on a CT/MRI scan. The primary tumor is not considered measurable disease. Metastatic lesions within a prior radiation field are acceptable as long as disease has progressed in the radiation field by RECIST criteria. The same imaging modality performed at baseline (CT or MRI) will be repeated at subsequent imaging. 5. ECOG performance status: 0-1; 6. Life expectancy ≥ 3 months. 7. Patients have adequate baseline organ and marrow function as defined by an absolute neutrophil count greater than 1500 cells per μL, platelet concentration of greater than 50 000 per μL, total bilirubin less than 1•5 times the upper limit of normal (ULN), aspartate aminotransferase and alanine aminotransferase less than 2•5 times the ULN, and serum creatinine less than 1•5 times the ULN; 8. Signed consent forms voluntarily;
Exclusion criteria
1. Patients who have had prior allergic reaction to Apatinib; 2. Patients undergoing therapy with other investigational agents. 3. Women who are pregnant or breastfeeding; 4. Patients with known brain metastases can be included in this clinical trial but brain lesions are not eligible as target or non target lesion; 5. Anticipated patient survival under 3 months; 6. Active severe infection or known chronic infection with HIV, hepatitis B virus, or hepatitis C virus; 7. Cardiovascular disease problems including unstable angina, therapy for life-threatening ventricular arrhythmia, myocardial infarction, stroke or congestive heart failure within the last 6 months; 8. The subject has had another active malignancy within the past five years except for cervical cancer in site, in situ carcinoma of the bladder or non-melanoma carcinoma of the skin; 9. Clinically significant and uncontrolled major medical conditions including but not limited to: active uncontrolled infection, symptomatic congestive heart failure, Unstable angina pectoris or cardiac arrhythmia, psychiatric illness/ social situation that would limit compliance with study requirements; any medical condition, which in the opinion of the study investigator places the subject at an unacceptably high risk for toxicities; 10. Patients with any other concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The proportion of patients with response (CR, PR, SD and PD based on RECIST version 1.0) assessed at 5-6 weeks after the initiation of treatment. | week 5- week 6 |
Secondary
| Measure | Time frame |
|---|---|
| The number of participants with adverse events from the date of enrollment until 2 years from the opening of the study. | year 0- year 2 |
| The proportion of patients alive (overall survival rate) from the date of enrollment until date of death from any cause, assessed up to 2 years from the opening of the study. | year 0- year 2 |
Countries
China
Contacts
Primary ContactShixiu Wu, MD
Backup ContactTao Song, Dr
Outcome results
None listed