Radiation Therapy and Cisplatin With or Without Cetuximab in Treating Patients With Stage IB, Stage II, or Stage IIIB Cervical Cancer (CETUXICOL)

Institut Curie

Status and phase

Completed

Phase 2

Conditions

Cervical Cancer

Treatments

Drug: cisplatin

Biological: cetuximab

Study type

Interventional

Funder types

Other

Identifiers

NCT00957411

CLCC-IC-2007-04 (Other Identifier)

2008-001053-18 (EudraCT Number)

CDR0000651250

Details and patient eligibility

About

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. It is not yet known whether radiation therapy given together with cisplatin is more effective with or without cetuximab in treating patients with cervical cancer.

PURPOSE: This randomized phase II trial is studying giving radiation therapy together with cisplatin to see how well it works compared with radiation therapy and cisplatin given together with cetuximab in treating patients with stage IB, stage II, or stage IIIB cervical cancer.

Full description

OBJECTIVES:

Primary

Evaluate the efficacy of treatment with cetuximab and a standard radiochemotherapy regimen (pelvic radiotherapy and cisplatin) in patients with stage IB2, II, and IIIB cervical cancer by evaluating the number of patients without recurrence at 2 years.

Secondary

Analyze the tumor response by MRI after external radiotherapy.
Assess the tolerance of cetuximab and standard radiochemotherapy in patients not previously treated and in generally good condition.
Study the correlation between treatment response and analysis of EGFR mutations (exons 18-21 of the tyrosine kinase domain including the two hot spots L858R and E746-A750).
Study the correlation between treatment response and evaluation of number of copies of the EGFR gene.
Study the correlation between treatment response and analysis of mutations of codons 12 and 13 of KRAS2 by direct sequencing.
Study the correlation between treatment response and research of DNA sequences of human papillomavirus.
Study the correlation between treatment response and overexpression of EGFR and COX2 (centralized) by IHC.
Study the correlation between treatment response and characterization of a genomic signature (genome, transcriptome, and Affymetrix chips from samples frozen in liquid nitrogen).
Collect tumor samples for molecular analysis.

OUTLINE: This is a multicenter study. Patients are stratified according to planned surgery (yes vs no) and are randomized to 1 of 2 treatment arms.

Arm I: Patients receive cisplatin IV over 1 hour once weekly during weeks 1-6. Patients also undergo pelvic radiotherapy 5 days a week during weeks 2-5 or 2-6.
Arm II: Patients receive cisplatin and undergo radiotherapy as in arm I. Patients also receive cetuximab IV over 1 hour once weekly during weeks 1-6.

After 6-8 weeks of study treatment, patients continue treatment as recommended by their center (i.e., utero-vaginal brachytherapy, additional radiotherapy, or surgery).

Tumor tissue and blood samples are collected for further analysis.

After completion of study treatment, patients are followed at 3-4 weeks and then every 4 months for 2 years.

Enrollment

76 patients

Sex

Female

Ages

18 to 120 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

Diagnosis of cervical cancer
- Squamous cell carcinoma or adenocarcinoma
- Stage IB2-IIIB disease
- Not immediately operable
Origin of the tumor and presence of measurable target lesion according to RECIST criteria confirmed by T2-weighted MRI
Data imaging scan and PET scan (optional) confirmed absence of lumbo-aortic adenopathy
No other associated pathology that would preclude study treatment

PATIENT CHARACTERISTICS:

WHO performance status 0-1
Hemoglobin > 10 g/dL
ANC > 1,500/mm^3
Platelet count > 100,000/mm^3
Alkaline phosphatase < 2 times normal
Total bilirubin < 1.5 times normal
Creatinine < 130 μmol/L
Creatinine clearance ≥ 60 mL/min
Normal vital functions
Not pregnant
Fertile patients must use effective contraception
Able to provide the imaging exams on CD ROM (DICOM 3.0 or higher) for centralized review
No history of another cancer that recurred within the past 5 years except for basal cell carcinoma of the skin or carcinoma in situ of the cervix
No absolute contraindication to MRI (i.e., claustrophobia, pacemaker, or cochlear implant)
No geographical, social, or psychological situations that preclude study follow up
Not deprived of liberty or under guardianship
Receiving benefits from a social security system

PRIOR CONCURRENT THERAPY:

No prior treatment (i.e., chemotherapy, radiotherapy, immunotherapy, hormonal therapy, or, especially, therapy with an investigational agent) for this cancer
No concurrent participation in a clinical trial with an experimental agent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

76 participants in 2 patient groups

Arm I

Active Comparator group

Description:

Patients receive cisplatin IV over 1 hour once weekly during weeks 1-6. Patients also undergo pelvic radiotherapy 5 days a week during weeks 2-5 or 2-6.

Treatment:

Drug: cisplatin

Arm II

Experimental group

Description:

Patients receive cisplatin and undergo radiotherapy as in arm I. Patients also receive cetuximab IV over 1 hour once weekly during weeks 1-6.

Treatment:

Biological: cetuximab

Drug: cisplatin