Radiation Therapy and Capecitabine With or Without Oxaliplatin in Treating Patients Who Are Undergoing Surgery for Stage II or Stage III Rectal Cancer

OBJECTIVES:

Primary

• Compare the efficacy of neoadjuvant chemoradiotherapy comprising radiotherapy and capecitabine with vs without oxaliplatin followed by total mesorectal excision, in terms of the rate of complete surgical resection, in patients with resectable stage II or III rectal cancer.

Secondary

• Compare overall and disease-free survival of patients treated with these regimens.
• Compare clinical tumor response in patients treated with these regimens.
• Compare acute and late toxicity of these regimens in these patients.
• Determine biological parameters that predict tumor response and treatment-related toxicity in patients treated with these regimens.
• Compare sphincter preservation and function in patients treated with these regimens.

OUTLINE: This is a randomized, controlled, multicenter study. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients undergo radiotherapy once daily 5 days a week and receive capecitabine once daily 5 days a week in weeks 1-5.
• Arm II: Patient undergo radiotherapy and receive capecitabine as in arm I. Patients also receive oxaliplatin once weekly in weeks 1-5.

All patients undergo total mesorectal excision 6 weeks after completion of chemoradiotherapy.

PROJECTED ACCRUAL: A total of 590 patients will be accrued for this study.

DISEASE CHARACTERISTICS:

• Histologically confirmed adenocarcinoma of the rectum

• T3-4, N0-2, M0 disease by endorectal ultrasound

• T2 disease located in the low rectum allowed provided lower pole is ≤ 6 cm from the anal verge
• Tumor must be accessible to digital rectal examination (i.e., tumor located at low- or mid-rectum)
• Resectable disease treatable with chemoradiotherapy

• No unresectable disease (i.e., T4 disease with high risk for incomplete gross resection [i.e., R2])

PATIENT CHARACTERISTICS:

Age

• 18 to 80

Performance status

• ECOG 0-2

Life expectancy

• Not specified

Hematopoietic

• WBC ≥ 1,500/mm^3
• Platelet count ≥ 100,000/mm^3
• Hemoglobin > 10 g/dL

Hepatic

• Alkaline phosphatase normal
• Bilirubin normal

Renal

• Creatinine ≤ 130 μmol/L
• No severe renal insufficiency

Cardiovascular

• No cardiac insufficiency
• No symptomatic coronary artery disease

Other

• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No contraindication to study treatment
• Prior acute intestinal obstruction allowed provided patient underwent surgical diversion with stoma
• No history of other cancer except basal cell skin cancer or carcinoma in situ of the cervix
• No peripheral neuropathy
• No uncontrolled diabetes
• No other uncontrolled severe disease
• No geographical, social, or psychological condition that would preclude study follow-up

PRIOR CONCURRENT THERAPY:

Biologic therapy

• Not specified

Chemotherapy

• No prior chemotherapy for cancer
• No other concurrent chemotherapy

Endocrine therapy

• Not specified

Radiotherapy

• No prior radiotherapy for cancer

Surgery

• Not specified

Other

• No concurrent phenytoin
• No concurrent participation in another clinical trial of an experimental medical treatment