Cetuximab, Oxaliplatin, Fluorouracil, and Radiation Therapy in Treating Patients With Stage II or Stage III Esophageal Cancer

NCT ID: NCT00425425

Last Updated: 2014-05-01

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 43 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-07-31
• Study Completion Date: 2015-05-31

Brief Summary

RATIONALE: 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. Cetuximab may also make tumor cells more sensitive to radiation therapy. Drugs used in chemotherapy, such as oxaliplatin and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving cetuximab, chemotherapy, and radiation therapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

PURPOSE: This phase I/II trial is studying the side effects and best dose of oxaliplatin and fluorouracil when given together with cetuximab and radiation therapy and to see how well they work in treating patients with stage II or stage III esophageal cancer.

Detailed Description

OBJECTIVES:

Primary

• Determine the maximum tolerated dose of oxaliplatin and fluorouracil when administered with cetuximab and radiotherapy in patients with stage II or III squamous cell carcinoma of the esophagus. (Phase I)
• Determine the response rate in patients treated with this regimen. (Phase II)

Secondary

• Determine the toxicity of this regimen in these patients.
• Determine the postoperative complication rate and lethality in patients treated with this regimen.
• Determine the R0 resection rate in patients treated with this regimen.
• Determine the overall survival of patients treated with this regimen.
• Determine the event-free survival of patients treated with this regimen.
• Determine the metabolic response rate in patients treated with this regimen.

OUTLINE: This is a phase I, dose-escalation study of oxaliplatin and fluorouracil followed by an open-label, phase II study.

• Phase I: Patients receive cetuximab IV over 60-90 minutes on days -15, -8, 1, 8, 15, 22, and 29; oxaliplatin IV over 120 minutes on days 1, 8, 22, and 29; and fluorouracil IV continuously on days 1-5, 8-12, 15-19, 22-26, and 29-33. Patients undergo radiotherapy on days 1-5, 8-12, 15-19, 22-26, and 29-33. Patients then undergo radical esophagectomy 29-42 days after the completion of chemoradiotherapy.

Cohorts of 3-6 patients receive escalating doses of oxaliplatin and fluorouracil 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.

• Phase II: Patients receive oxaliplatin and fluorouracil as in phase I at the MTD determined in phase I. Patients also receive cetuximab and undergo radiotherapy and radical esophagectomy as in phase I.

After completion of study therapy, patients are followed every 3 months for 2 years and then every 6 months for 3 years.

PROJECTED ACCRUAL: A total of 43 patients will be accrued for this study.

Conditions

Esophageal Cancer

Study Design

• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

cetuximab

Intervention Type: BIOLOGICAL

fluorouracil

Intervention Type: DRUG

oxaliplatin

Intervention Type: DRUG

conventional surgery

Intervention Type: PROCEDURE

neoadjuvant therapy

Intervention Type: PROCEDURE

radiation therapy

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed squamous cell carcinoma of the esophagus, meeting the following criteria:

• Locally advanced disease (T3-T4, N0-N+ [T2, N0 for cervical esophageal carcinoma])
• Potentially resectable disease
• No distant metastases (M1b)
• No tumor infiltration of the tracheobronchial system
• Bartels preoperative risk analysis < 22

PATIENT CHARACTERISTICS:

• ECOG performance status (PS) 0-1 or Karnofsky PS 70-100%
• Creatinine ≤ 1.5 mg/dL OR creatinine clearance > 60 mL/min
• Bilirubin ≤ 1.5 mg/dL
• ALT and AST ≤ 2 times upper limit of normal (ULN)
• Alkaline phosphatase ≤ 2 times ULN
• WBC ≥ 3,000/mm³
• Granulocyte count ≥ 2,000/mm³
• Platelet count ≥ 100,000/mm³
• No pre-existing polyneuropathy > grade 1
• No active uncontrolled infection
• PaO_2 ≥ 60 mm Hg on room air
• FEV_1 ≥ 60% of normal
• No New York Heart Association class II-IV cardiac insufficiency
• Ejection fraction ≥ 35%
• No angina pectoris (at rest or under stress) unexplained by interventional cardiology
• No myocardial infarction within the past 6 months
• No histologically confirmed liver cirrhosis
• No other malignancy within the past 5 years except carcinoma in situ of the cervix or nonmelanomatous skin cancer
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

• No prior chemotherapy
• No prior radiotherapy to the thorax region
• No current esophageal stent

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Technical University of Munich

OTHER

Sponsor Role: lead

Principal Investigators

Florian Lordick, MD

Role: STUDY_CHAIR

Technical University of Munich

Locations

Charite University Hospital - Campus Virchow Klinikum

Berlin, , Germany

Universitaetsklinikum Giessen und Marburg GmbH - Marburg

Marburg, , Germany

Klinikum Rechts Der Isar - Technische Universitaet Muenchen

Munich, , Germany

Countries

Germany

Other Identifiers

KRDI-TUM-OE7-432-LOR-0033-I

Identifier Type: -

Identifier Source: secondary_id

EU-20658

Identifier Type: -

Identifier Source: secondary_id

EUDRACT-2006-001097-24

Identifier Type: -

Identifier Source: secondary_id

CDR0000516821

Identifier Type: -

Identifier Source: org_study_id