Skip to content

A prospective multicenter study on 3D image-guided brachytherapy for locally advanced cervical cancer

A prospective multicenter study on 3D image-guided brachytherapy for locally advanced cervical cancer - A prospective multicenter study on 3D image-guided brachytherapy for locally advanced cervical cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000016140
Enrollment
60
Registered
2015-01-06
Start date
2014-09-04
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

Locally advanced cervical cancer (FIGO IIa2,IIb,III,IVa)

Interventions

External beam radiotherapy: 50 Gy / 25 fractions Image-guided brachytherapy: 18-24 Gy / 3-4 fractions Chemotherapy: weekly cisplatin 40 mg / m2 for 5 weeks.

Sponsors

Gunma University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Histologically diagnosed adenocarcinoma, adeno-squamous cell carcinoma, or squamous cell carcinoma of uterine cervix. 2. International Federation of Gynecology and Obstetrics (FIGO) Stage IIa2 , IIb , III, or IVA disease 3. No para-aortic lymph nodes >= 1 cm in minimum diameter on CT images 4. The tumor had to be grossly measurable by MRI. 5. Tumor size is >= 4 cm in diameter 6. Age between 20 and 75 years 7. Performance status 0 - 2 8. Patients with no histories of prior chemotherapy or pelvic surgery for cervical cancer 9. Normal organ function (WBC >= 3000/mm3,Hb >= 9.5g/dl, Plt>= 100,000/mm3, T-Bil.<= 1.5mg/dl, AST(GOT) and ALT(GPT) <= 100IU/dl, Cre <= 1.5mg/dl, CCR >= 50ml/min, ECG normal or require no treatment 10. Informed consent is obtained

Exclusion criteria

Exclusion criteria: 1. Tumor invasion to gastro-intestinal tract. 2. Uncontrolled infection in pelvis 3. Rectal invasion History of pelvic radiotherapy 4. Severe complicating illness 5. Active double cancer 6. Possibility of pregnancy or lactation period 7. medical, psychological or others reason that primary doctor think ineligible

Design outcomes

Primary

MeasureTime frame
Pelvic disease progression-free rate

Secondary

MeasureTime frame
Overall survival rate ,Local control rate, Incidence rate of acute adverse effects , Incidence rate of late adverse effect

Countries

Japan

Contacts

Public ContactTatsuya Ohno

Gunma University Department of Radiation Oncology

tohno@gunma-u.ac.jp(027)220-8383

Outcome results

None listed

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