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A multicenter prospective randomized controlled trial comparing radical surgery versus concurrent chemoradiotherapy in stage IIICr cervical cancer

A multicenter prospective randomized controlled trial comparing radical surgery versus concurrent chemoradiotherapy in stage IIICr cervical cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127185
Enrollment
Unknown
Registered
2026-06-26
Start date
2025-11-20
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Cervical cancer

Interventions

Experimental group:Radical hysterectomy

Sponsors

Cancer hospital chinese academy of medical sciences,shenzhen center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. The subjects voluntarily participated in this study, signed the informed consent form, had good compliance, and cooperated with the follow-up. 2. Female patients aged 18-65 years old. 3. Clinically diagnosed with FIGO (2018) stage IIICr cervical cancer (evaluated for lymph node metastasis through imaging examination). 4. ECOG status 0-1 / Karnofsky score >= 80. 5. Preoperative pathological diagnosis of cervical squamous cell carcinoma, cervical adenosquamous cell carcinoma or cervical adenocarcinoma. 6. Patients with cervical cancer who received initial treatment or those who underwent neoadjuvant chemotherapy (if PD-L1 positive / CPS score >= 1, immunotherapy combined with neoadjuvant chemotherapy was possible). 7. Preoperative imaging and physical examination showed no involvement of the parametrium and no involvement of the lower 1/3 of the vagina.

Exclusion criteria

Exclusion criteria: 1. Patients who have previously received pelvic/abdominal radiotherapy or chemotherapy; 2. CT, MRI or PET scans indicate distant metastasis; 3. Had a second malignant tumor in the past 5 years (excluding thyroid cancer or carcinoma in situ during the same period) or had any signs of recurrence or activity; 4. Have severe systemic diseases; 5. Clinically diagnosed with primary cervical cancer, FIGO (2018) stage IIB, IIIA, IIIB (with parametrial involvement, lower 1/3 of the vagina involvement and pelvic wall involvement); 6. Pregnant; 7. Any factor affecting informed consent, compliance with the research protocol or inability to follow up on schedule; 8. Have any active infectious diseases or incurable severe inflammation.

Design outcomes

Primary

MeasureTime frame
Progression-free survival;

Secondary

MeasureTime frame
Overall survival;Quality of life;Complications from surgery/radiation ± chemotherapy;The accuracy of radiological diagnosis of lymph nodes;Pelvic/retroperitoneal lymph node recurrence rate;

Countries

China

Contacts

Public ContactLi Sun

Cancer hospital chinese academy of medical sciences,shenzhen center

xjsunli@sina.com+86 755 6661 8168

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026