Cisplatin, Capecitabine, and Radiation Therapy With or Without Cetuximab in Treating Patients With Esophageal Cancer

• Status: Unknown status
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Drugs used in chemotherapy, such as cisplatin and capecitabine, work in different ways to kill tumor cells or stop them from growing. Radiation therapy uses high-energy x-rays to kill tumor cells. 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 stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether giving cisplatin together with capecitabine and radiation therapy is more effective with or without cetuximab in treating esophageal cancer.

PURPOSE: This randomized phase II/III trial is studying the side effects and how well giving cisplatin together with capecitabine, radiation therapy, and cetuximab works compared with giving cisplatin, capecitabine, and radiation therapy without cetuximab in treating patients with esophageal cancer.

• Phase: Phase 2/Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Wales Cancer Trials Unit
• Collaborator: Cancer Research UK
• Treatments: Capecitabine; Cetuximab; Cisplatin

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed carcinoma of the esophagus

• Adenocarcinoma

• Squamous cell

• Undifferentiated carcinoma

• Siewert type I tumor of the gastroesophageal junction

• Localized, nonmetastatic disease (T1-4, N0-1) confirmed by endoscopic ultrasound (EUS) and spiral CT scan

• Total disease length (primary and lymph nodes) < 10 cm by EUS

• Not suitable for surgery (either for medical reasons or patient's choice)

• No metastatic disease (i.e., M1a or M1b according to UICC TNM version 6)

• No significant (> 2 cm) extension of tumor into the stomach

PATIENT CHARACTERISTICS:

• WHO performance status 0-1

• Absolute neutrophil count ≥ 1,500/mm³

• White blood cell count ≥ 2,000/mm³

• Platelet count ≥ 100,000/mm³

• Hemoglobin ≥ 10 g/dL (should be corrected to > 10 g/dL before treatment)

• Serum bilirubin ≤ 1.5 times upper limit of normal (ULN)

• ALT/AST ≤ 2.5 times ULN

• Alkaline phosphatase ≤ 3 times ULN

• Glomerular filtration rate > 40 mL/min OR > 60 mL/min estimated by Cockcroft-Gault formula

• Adequate cardiac ejection fraction ≥ 40% by MUGA or ECHO

• FEV_1 ≥ 1 L by spirometry

• Not pregnant

• Negative pregnancy test

• Fertile patients must use effective contraception

• No malignancy within the past 5 years

• No unstable angina, uncontrolled hypertension, cardiac failure, or other clinically significant cardiac disease

• No major trauma within the past 4 weeks

• No known dihydropyrimidine dehydrogenase deficiency

• No hearing impairment or sensory-motor neuropathy > grade 2

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• At least 4 weeks since prior sorivudine and analogues

• At least 4 weeks since prior major surgery

• At least 4 weeks since prior monoclonal antibody

• At least 3 months since prior radiotherapy

• No prior treatment for invasive esophageal carcinoma or gastroesophageal junction carcinoma (not including photodynamic therapy or laser therapy for high-grade dysplasia/carcinoma in situ)

• No other prior treatment for this malignancy that would compromise the ability to deliver definitive mediastinal chemoradiotherapy or compromise survival