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A retrospective, single-center clinical study on the comparison of uterine artery chemoembolization with cisplatin-loaded drug microspheres combined with paclitaxel intravenous chemotherapy versus blank microsphere uterine artery embolization combined with cisplatin and paclitaxel intravenous chemotherapy followed by surgery and radiotherapy in the treatment of stage IB3-IIA2 cervical cancer

A retrospective, single-center clinical study on the comparison of uterine artery chemoembolization with cisplatin-loaded drug microspheres combined with paclitaxel intravenous chemotherapy versus blank microsphere uterine artery embolization combined with cisplatin and paclitaxel intravenous chemotherapy followed by surgery and radiotherapy in the treatment of stage IB3-IIA2 cervical cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129054
Enrollment
Unknown
Registered
2026-07-29
Start date
2026-08-08
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Stage IB3-IIA2 cervical cancer

Interventions

Observation Group B(Blank microsphere uterine artery embolization combined with cisplatin + paclitaxel systemic intravenous chemotherapy):None
Observation Group A(Uterine artery embolization with drug-loaded microspheres containing cisplatin combined with systemic intravenous chemotherapy with paclitaxel):None

Sponsors

The First Affiliated Hospital,Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The pathological diagnosis of cervical cancer is classified as locally advanced cervical cancer (IB3-IIA2) according to the FIGO staging system; 2.The age range is 18 to 80 years old; 3. Received DEB-TGA or concurrent radiotherapy treatment, and complete clinical and pathological information before and after the treatment.

Exclusion criteria

Exclusion criteria: 1. Severe effusion or pleural effusion; 2. Contraindications to cisplatin or paclitaxel; 3. Patients with severe mental disorders or severe cardiac, hepatic or renal dysfunction; 4. Patients complicated with other malignant tumors; 5. Uncontrollable diabetes or hypertension; 6. Contraindications for arterial perforation operation; 7. Presence of sepsis or severe infection; 8. Pregnant or lactating women; 9. Patients with severe coagulation dysfunction or anemia.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate ,Disease Control Rate;Safety and side effects of toxicity;Re-resection rate;

Secondary

MeasureTime frame
2-year Progression-Free Survival (PFS);Overall Survival (OS);

Countries

China

Contacts

Public ContactJi Weiming

The First Affiliated Hospital,Sun Yat-sen University

jiwm@mail.sysu.edu.cn+86 10 12345678

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026