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Study on the efficacy and safety of bevacizumab combination regimen (chemotherapy or chemoradiotherapy) in the treatment of gynecological tumors in real diagnosis and treatment environment

Study on the efficacy and safety of bevacizumab combination regimen (chemotherapy or chemoradiotherapy) in the treatment of gynecological tumors in real diagnosis and treatment environment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101038
Enrollment
Unknown
Registered
2025-04-18
Start date
2023-08-23
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Ovarian cancer, cervical cancer, fallopian tube cancer, primary peritoneal adenocarcinoma and other gynecological tumors

Interventions

Observation group:None

Sponsors

Henan Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. July 1, 2022 ~ January 31, 2024; 2. Gynecological tumors such as cervical cancer, ovarian cancer, fallopian tube cancer, and primary peritoneal adenocarcinoma confirmed by imaging or histological pathological examination; Bevacizumab is indicated according to clinical diagnosis and treatment routine; 3. ECOG score of 0-1; 4. Receiving bevacizumab combination therapy (including chemotherapy, chemoradiotherapy, etc.).

Exclusion criteria

Exclusion criteria: 1. Other malignant tumors that are not gynecological tumors such as cervical cancer, ovarian cancer, fallopian tube cancer, and primary peritoneal adenocarcinoma; 2. Incomplete clinical case data (lack of efficacy evaluation information, adverse reaction evaluation information).

Design outcomes

Primary

MeasureTime frame
The number and proportion of users of bevacizumab combined with chemotherapy or radiotherapy;Objective response rate;

Secondary

MeasureTime frame
Type and severity of adverse reactions;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactChao Hongtu

HenanCancerHospital

13733896566@163.com+86 371 65587320

Outcome results

None listed

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