Overview

Clinical Study of Apatinib in the Treatment of Advanced Ovarian Cancer After the Failure of Standard Chemotherapy

Status:
Unknown status
Trial end date:
2020-06-01
Target enrollment:
0
Participant gender:
Female
Summary
To Observe and Evaluate the Efficacy and Safety of Apatinib in Patients With Advanced Ovarian Cancer After the Failure of Standard Chemotherapy
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Anhui Provincial Hospital
Treatments:
Apatinib
Criteria
Inclusion Criteria:

1. ovarian cancer confirmed by pathology;

2. At least one measuring lesion (RECIST 1.1) or ascites (B ultrasound);

3. Patients with advanced ovarian cancer who failed in standard treatment. Note: Advanced
ovarian cancer with recurrence of platinum-resistant drug and having no possibility of
surgery

4. Baseline blood routine and biochemical indicators meet the following criteria:

① ANC ≥ 1.5 × 109 / L;

- HB ≥ 90g / L;

- PLT ≥ 100 × 109 / L; ④ ALB≥30g / L;

- TBIL≤1.5 times the upper limit of normal (ULN); ⑥ ALT and AST<2 × ULN;
⑦ Plasma Cr<1.5 × ULN

5. No blood transfusion , blood products, G-CSF and other hematopoietic stimulation
factors were used in 14 days ;

6. The expected survival time is longer than 3 months;

7. The pregnancy test (serum or urine)should be carried out for women in childbearing age
before 7 days into the group and the results were negative, and willing to use
appropriate methods of contraception during the test and after 8 weeks out of group

8. The subjects volunteered to participate in this study, signed informed consent,
followed up with good compliance .

Exclusion Criteria:

1. Allergies to apatinib and/or its excipients

2. People with high blood pressure and antihypertensive drug treatment can not drop to
normal range (systolic blood pressure > 140 mmHg, diastolic blood pressure > 90 mmHg),
with level-1 above coronary heart disease, arrhythmia over class I (including QTc
lengthened men > 450 ms, women > 470 ms).

3. According to NYHA standard, Ⅲ - Ⅳ cardiac insufficiency, or LVEF < 50%;

4. Various factors that affect oral drugs (such as inability to swallow, nausea,
vomiting, chronic diarrhea, intestinal obstruction, etc.);

5. Patients with a clear tendency of gastrointestinal bleeding, including the following
situations: local active ulcer lesions, and fecal occult blood (++); Patients with
black stool and hematemesis in 2 months;

6. Abnormal coagulation function (INR>1.5, APTT>1.5 ULN), with bleeding
tendency;Hereditary or acquired bleeding and thrombosis tendencies (such as
hemophilia,coagulation dysfunction, thrombocytopenia, hypersplenism, etc.);

7. Long-term unhealed wounds or fractures; Major surgery or severe traumatic injury,
fracture or ulcer in 4 weeks;

8. With abdominal fistula, gastrointestinal perforation or abdominal abscess;Active
patients with HBV or HCV;

9. Active brain metastases, meningitis, cancer patients with spinal cord compression, CT
or MRI examination revealed brain or soft meningeal disease (21 days before the drug
treatment; the symptoms of patients with stable brain metastases can into the group,
but need to be confirmed by the cerebral MRI, CT or vein imaging evaluation no
cerebral hemorrhage).

10. CT or MRI showed that the tumor lesion was less than 5 mm away from the large vessel,
or the lesion invaded local large vessels;

11. Pregnant or lactating women;

12. Patients with a history of psychotropic substance abuse or have mental disorders;

13. According to the researchers' judgment, patients who have serious harm to the
patient's safety or affect the patients for completing the research;

14. Subjects considered inappropriate by the researchers.