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Clinical efficacy and safety of antiangiogenic drugs in the treatment of platinum-resistant and biochemical recurrent ovarian cancer

Clinical efficacy and safety of antiangiogenic drugs in the treatment of platinum-resistant and biochemical recurrent ovarian cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000031541
Enrollment
Unknown
Registered
2020-04-04
Start date
2018-09-01
Completion date
Unknown
Last updated
2020-04-06

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

Conditions

Platinum resistance and biochemical recurrence of ovarian cancer

Interventions

Case series:antiangiogenic drugs

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. aged between 20 and 75 years; 2. all patients underwent tumor cell ablation and were diagnosed as epithelial ovarian cancer by histopathology. 3. the patient has received at least first-line platinum-based chemotherapy with evidence of recurrence and has stopped using platinum-based drugs for less than 6 months, including refractory ovarian cancer with disease progression during the use of platinum-based chemotherapy; 4. good physical condition: Eastern Cooperative Oncology Group (ECOG) score =3 months; 6. there are measurable lesions; 7. volunteered to participate in this project, agreed to the treatment follow-up and reexamination of the center, and did not participate in other clinical researchers within 3 months.

Exclusion criteria

Exclusion criteria: 1) allergy to antiangiogenic targeted drugs; 2) patients with serious heart disease or history (angina pectoris, intractable hypertension, congestive heart failure, myocardial infarction, high risk uncontrolled arrhythmia, and heart valve disease); 3) inflammation, unhealed wounds, ulcers or bleeding diseases; 4) the second primary malignant tumor; 5) patients with uncontrollable neurological, mental illness or mental disorder, poor compliance and inability to cooperate and describe treatment responses; 6) patients who also participate in other clinical trials; 7) other circumstances in which the investigator considers the patient inappropriate to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Countries

China

Contacts

Public ContactZhang Mei

The First Affiliated Hospital of Anhui Medical University

2239824941@qq.com+86 13856990019

Outcome results

None listed

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