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Comparison of radical radiotherapy with or without chemotherapy for poor prognosis carcinoma of cervix

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN38929731
Enrollment
Unknown
Registered
2001-07-01
Start date
1992-01-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Cervix cancer Cancer Cervix

Interventions

1. Arm A: Chemotherapy with methotrexate and cisplatinum repeated every 14 days for three cycles. Radiotherapy consisting of a course of external beam therapy followed by intracavity brachytherapy to

Sponsors

Cancer Research UK (CRUK) (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Histologically diagnosed squamous cell carcinoma of the cervix uteri 2. International Federation of Gynecology and Obstetrics (FIGO) stage III, IVa or bulky stage II 3. No evidence of extra pelvic spread 4. Aged <70 years 5. World Health Organisation (WHO) performance 0-2 6. Suitable for radical radiotherapy 7. Suitable for chemotherapy 8. Adequate haematological and renal function 9. No history of previous malignancy, excluding successfully treated squamous and basal cell carcinoma of skin or carcinoma in situ of the cervix 10. No previous chemotherapy or radiotherapy 11. No contraindications to treatment

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

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