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Retrospective real-world clinical study on the efficacy and safety of bevacizumab combined with chemotherapy/radiotherapy/PARP inhibitors in the treatment of gynecological tumors in cervical and ovarian cancer

Retrospective real-world clinical study on the efficacy and safety of bevacizumab combined with chemotherapy/radiotherapy/PARP inhibitors in the treatment of gynecological tumors in cervical and ovarian cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084934
Enrollment
Unknown
Registered
2024-05-28
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

cervical carcinoma and Ovarian Carcinoma

Interventions

Treatment group:Administer bevacizumab for treatment

Sponsors

Jiangnan University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Visit from January 1, 2023 to December 31, 2023 2) Age = 18 years old 3) Cervical or ovarian cancer patients verified by histology or cytology 4) Indications for the use of bevacizumab based on clinical diagnostic criteria 5) ECOG score 0-1 points 6) The subjects received a treatment regimen containing bevacizumab in combination with chemotherapy, radiation therapy, etc

Exclusion criteria

Exclusion criteria: 1) Patients with concomitant malignant tumors 2) Individuals who are allergic to bevacizumab and its excipients 3) Severe injuries to the liver, kidneys, hematopoiesis, and cardiovascular system 4) Pregnant or lactating women 5) Patients with previous gastrointestinal perforation and fistula, including gallbladder perforation, who have undergone major surgery four weeks before medication, or whose wounds have not healed four weeks before medication 6) Patients with tumor infiltration into large blood vessels or proximal tracheal and bronchial networks, or recent occurrence of pulmonary hemorrhage/hemoptysis (>1/2 teaspoon of fresh red blood), or other risks of major bleeding; 7) Researchers believe that other conditions that are not suitable for treatment, such as active tuberculosis, cardiovascular accidents, cerebrovascular accidents, drug use, alcoholism, and other bad habits

Design outcomes

Primary

MeasureTime frame
Progression free survival;Objective relief rate;Describe the number and proportion of users of bevacizumab combined with chemotherapy/radiotherapy/PARP inhibitors in cervical and ovarian cancer subjects, respectively;

Secondary

MeasureTime frame
Adverse reaction incidence rate;Types and severity of adverse reactions;

Countries

China

Contacts

Public ContactJinjin YU

Jiangnan University Affiliated Hospital

yujjwx@126.com+86 159 5158 0901

Outcome results

None listed

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