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TERMINATED
NCT00421096
PHASE2

Radiochemotherapy Followed by Adjuvant Chemotherapy Based on Gemcitabine in Uterine Cervical Cancer

Sponsor: Centre Oscar Lambret

View on ClinicalTrials.gov

Summary

The scope of the trial is to assess the efficacy of the association gemcitabine-cisplatin + radiotherapy followed by an adjuvant chemotherapy

Official title: Stage IB2 to IVA Uterine Cervical Cancer: Phase 2 Study to Assess a New Therapeutic Sequence Associating a Radiochemotherapy Followed by Adjuvant Chemotherapy Based on Gemcitabine

Key Details

Gender

FEMALE

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

19

Start Date

2005-05

Completion Date

2011-12

Last Updated

2026-09-17

Healthy Volunteers

No

Interventions

DRUG

Gemcitabine

125 mg/m² at day 1, 8, 15, 21 and 28, 2 hours before radiotherapy.

PROCEDURE

Radiotherapy

45Gy (5 x 1,8Gy/week) on pelvic area +/- boost (10 to 15Gy) +/- 45Gy (5 x 1,8Gy/week)on lumbo-aortic area

DRUG

Cisplatin

40 mg/m² at day 1, 8, 15, 21 and J28 before Gemcitabine and with a hyperhydration

Locations (2)

Centre Leonard de Vinci

Dechy, France

Centre Oscar Lambret

Lille, France