Radiation Therapy, Irinotecan, and Cetuximab in Treating Patients Who Are Undergoing Surgery for Stage III or Stage IV Rectal Cancer

NCT ID: NCT00392470

Last Updated: 2011-05-25

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-08-31

Brief Summary

RATIONALE: Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Drugs used in chemotherapy, such as irinotecan, 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. Giving radiation therapy together with irinotecan and cetuximab before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

PURPOSE: This phase I trial is studying the side effects and best dose of irinotecan when given together with cetuximab and radiation therapy in treating patients who are undergoing surgery for stage III or stage IV rectal cancer.

Detailed Description

OBJECTIVES:

Primary

• Determine the toxicity of irinotecan hydrochloride and cetuximab in patients with stage III or IV rectal cancer undergoing conformal or intensity-modulated radiotherapy.

Secondary

• Determine the rate of pathologic response and histological degree of tumor regression in patients treated with this regimen.
• Determine the complete resection rate (R0) in patients treated with this regimen.
• Determine the sphincter preservation rate in patients treated with this regimen.
• Determine the 30-day postoperative complication rate in patients treated with this regimen.
• Determine the local and distant relapse rate and site of disease failure in patients treated with this regimen.
• Estimate the predictive value of fludeoxyglucose F 18 positron emission tomography/CT scan for treatment response compared to endoscopic ultrasonography (EUS), CT scan, and MRI in patients treated with this regimen.
• Determine the late toxicity of this regimen in these patients.
• Determine the clinical (radiological) tumor response (i.e., MRI, CT scan, EUS) in patients treated with this regimen.

OUTLINE: This is a dose-escalation study of irinotecan hydrochloride.

Patients receive cetuximab IV over 1-2 hours on days 1, 8, 15, 22, 29, 36, and 43 followed by irinotecan hydrochloride IV over 30 minutes on days 1, 8, 15, 22, and 29. Patients also undergo conformal radiotherapy or intensity-modulated radiotherapy on days 1-5 for 5 weeks. Patients undergo radical surgery 3-4 weeks after completion of neoadjuvant therapy.

Cohorts of 3-6 patients receive escalating doses of irinotecan hydrochloride until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

After completion of study treatment, patients are followed periodically for at least 5 years.

PROJECTED ACCRUAL: A total of 20 patients will be accrued for this study.

Conditions

Colorectal Cancer

Study Design

• Primary Study Purpose: TREATMENT

Interventions

cetuximab

Intervention Type: BIOLOGICAL

irinotecan hydrochloride

Intervention Type: DRUG

conventional surgery

Intervention Type: PROCEDURE

neoadjuvant therapy

Intervention Type: PROCEDURE

3-dimensional conformal radiation therapy

Intervention Type: RADIATION

intensity-modulated radiation therapy

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed adenocarcinoma of the rectum

• T3-4 and/or N+ (stage IIIB, IIIC, or IV disease)
• Liver or lung metastasis allowed
• No recurrent disease

PATIENT CHARACTERISTICS:

• WHO performance status 0 or 1
• Hematologic, liver, and renal function normal
• Considered fit for chemotherapy, radiotherapy, and surgery
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception during and for 3 months after completion of study treatment
• No symptomatic heart disease or myocardial infarction during the past 6 months
• No chronic inflammatory bowel disease
• No malignant tumor during the past 5 years except for completely surgically resected carcinoma of the cervix or squamous cell carcinoma of the skin
• No other concurrent malignant tumor

PRIOR CONCURRENT THERAPY:

• No prior chemotherapy or radiotherapy for rectal cancer
• No prior radiotherapy to the pelvis

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 74 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Hospitalier Universitaire Vaudois

OTHER

Sponsor Role: lead

Principal Investigators

Michael Montemurro, MD

Role: STUDY_CHAIR

Centre Hospitalier Universitaire Vaudois

Locations

Kantonsspital Aarau

Aarau, , Switzerland

Site Status: RECRUITING

Institut Ludwig de Recherche sur le Cancer

Épalinges, , Switzerland

Site Status: RECRUITING

Centre Hospitalier Universitaire Vaudois

Lausanne, , Switzerland

Site Status: RECRUITING

Countries

Switzerland

Facility Contacts

Peter Moosmann, MD, PhD

Role: primary

peter.moosmann@ksa.ch

41-62-838-6051

Curzio Ruegg, MD

Role: primary

44-412-1692-5853

Michael Montemurro, MD

Role: primary

41-21-314-4530

Other Identifiers

CHUV-CEPO-CORCC-204-5

Identifier Type: -

Identifier Source: secondary_id

EU-20645

Identifier Type: -

Identifier Source: secondary_id

PFIZER-CHUV-CAPO-CARK-204-5

Identifier Type: -

Identifier Source: secondary_id

MERCK-CHUV-CAPO-CARK-204-5

Identifier Type: -

Identifier Source: secondary_id

CDR0000512816

Identifier Type: -

Identifier Source: org_study_id