Overview

CAmpto-CISplatine Plus Radiotherapy in Advanced Cervix Cancer : Search of Tolerated Maximum Dose of Campto

Status:
Completed
Trial end date:
2005-11-01
Target enrollment:
0
Participant gender:
Female
Summary
Search of maximum tolerated irinotecan dose in association with cisplatin and pelvic radiotherapy in patients with an advanced cervix cancer.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
ARCAGY/ GINECO GROUP
Treatments:
Cisplatin
Irinotecan
Criteria
Inclusion Criteria:

- Histologically proven primitive epidermoid or andenocarcinoma Cervix

- FIGO stage IIB (obviously parameter attack), III or IVA

- No previous chemotherapy nor radiotherapy

- Patient for whom a radiochemotherapy is envisaged as first intention treatmentof her
cervix carcinoma

- PS ECOG < 2

- Life expectancy > 12 weeks

- Written consent given

Exclusion Criteria:

- Other malignant cervix tumor histology

- Visceral remotly metastasis

- Other malignant tumor since 5 years, except spino or baso-cellular treaten and cured
cancer

- Anormal labs values

- Peripheric neuropathy CTC > 2

- Auditory loss > 2

- Cardiopathy

- Inflammatory digestive pathology

- Evolutive infection

- Other experimental concommitant treatment

- Lacting or pregnant women