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Apatinib plus Docetaxel for Treating Taxol Resistant Patients with Ovarian Cancer

Apatinib plus Docetaxel for Treating Taxol Resistant Patients with Ovarian Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17011622
Enrollment
Unknown
Registered
2017-06-10
Start date
2017-06-12
Completion date
Unknown
Last updated
2017-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ovarian cancer

Interventions

treatment group:apatinib combined with docetaxel

Sponsors

Changhai Hospital of Second Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. aged from 18 to 75 years old. 2. the pathological diagnosis of epithelial ovarian cancer. 3. by detecting specific drug resistance or a recent application progressed after taxol chemotherapy. 4. ECOG score(PS) from 0 to 2 point. 5. main viscera function is normal,t as the following requirements: (1) the blood routine examination, must be in accordance with no blood transfusion (14 days): HB=90g/L; ANC=1.5×109/L; PLT=80×109/L. (2) biochemical inspection must meet the following standards: BIL<1.5×ULN; ALT and AST<2.5×ULN; if liver metastases occured, ALT and AST<5×ULN; serum Cr=1×ULN. 6. expected lifetime=3 months. 7. agreed to participate in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. patients with hypertension, the antihypertensive drug treatment can not drop to normal range (systolic blood pressure > 140mmHg/diastolic blood pressure > 90mmHg), with a class II or higher coronary heart disease, arrhythmia (including QTc lengthened men > 450 ms, women > 470 ms) and cardiac insufficiency; 2. the influence factors of oral drug absorption, such as unable to swallow, chronic diarrhea and intestinal obstruction, etc.; 3. the patients with contraindications of apatinib or docetaxel; 4. the patients had a history of mental illness can't cooperation; 5. known allergic to the study medication; 6. patients are participanting in other drug trials.

Design outcomes

Primary

MeasureTime frame
ORR;DCR;

Secondary

MeasureTime frame
PFS;OS;QOL;ECOG score;symptoms of Ovarian cancer;

Countries

China

Contacts

Public ContactYu Chaoqin

Changhai Hospital of Second Military Medical University

chqyu81@163.com+86 13818390984

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026