Advanced Esophagus Cancer
Conditions
Brief summary
Subject ever received a standard chemotherapy solution progression or recurrence or can't tolerate chemotherapy with advanced esophageal squamous carcinoma.
Interventions
DRUGApatinib
Apatinib500 mg,po,qd,continuous dosing until PD, death or not tolerated toxicity.
Sponsors
Jiangsu HengRui Medicine Co., Ltd.
Henan Cancer Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* 1\. Age: 18 to 75 years old, men and women; * 2\. After histopathological and immunohistochemical examination diagnosis of esophageal squamous cell carcinomas. At least one measurable lesion after the treatment (the length to diameter of CT scan≥10 mm , accord with the requirement of RESCIST 1.1);the lesions of whom had not received radiotherapy. * 3\. Advanced esophageal squamous cell carcinoma without molecular targeted drug therapy; * 4\. ECOG PS:0-1; * 5\. Life expectancy≥12 weeks; * 6\. Patients who have disease progressed or relapsed after standard chemotherapy, or who have been unable to tolerate chemotherapy; * 7\. The main organs function properly, that is, meet the following criteria: 1. blood routine examination: HB≥90 g / L; (without blood transfusion during 14 days) ANC≥1.5×109 /L; PLT≥80×109 / L; 2. biochemical examination: ALB≥30g / L; (without infusion of albumin during 14 days) ALT and AST\<2ULN; TBIL≤1.5ULN; Plasma Cr≤1.5ULN; * 8\. The results of the serum pregnancy test of women in childbearing age must be negative in the 7 days prior to treatment; all patients (both male and female) should take adequate barrier contraception within the entire treatment and 4 weeks after treatment. * 9\. Subject should volunteer to join the study, sign the informed consent, have good compliance and cooperate with the follow-up; * 10\. Investigator believe that subject who can benefit.
Exclusion criteria
* 1\. In the past or at the same time with suffered from other malignancies; * 2\. Pregnant or lactating women; * 3\. Patients with high blood pressure and can't get a good control after antihypertensive drug therapy (systolic blood pressure\>150mmHg, diastolic blood pressure\>100mmHg); patients with grade Ⅱ or more myocardial ischemia or myocardial infarction, poorly controlled arrhythmia (including QTC interval≥450ms) and Ⅲ\ Ⅳ grade cardiac insufficiency according to NYHA; cardiac color Doppler ultrasonography: LVEF \<50%; * 4\. Unable to swallow, chronic diarrhea and intestinal obstruction, significantly affect the drug taking and absorption; * 5\. With a clear risk of gastrointestinal bleeding (such as locally active ulcer lesions, fecal occult blood above + +), history of gastrointestinal bleeding within 6 months, and unhealed wounds; * 6\. Central nervous system metastasis has occurred; * 7\. With abnormal coagulation function (PT\>16s, APTT\>43s, TT\>21s, Fbg\<2g/L), with bleeding tendency or receiving thrombolytic or anticoagulant therapy; * 8\. With mental illness, or mental history of drug abuse; * 9\. With anastomotic recurrence; * 10\. Patients who have participated in other drug clinical trials in 4 weeks; * 11\. Patients who have concomitant diseases that are seriously compromise the patient's safety or affect the patient to complete the study according to the researcher's judgment; * 12\. Patients those researchers believe not suitable for the inclusion.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Progress free survival | 24 months | Time subject into the group to tumor objective progression. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival | up to 24 months | Time subject into the group to die. |
Countries
China
Contacts
Primary ContactYing Liu
Outcome results
None listed