Combination Chemotherapy and Surgery in Treating Patients With Locally Advanced Stomach Cancer

Swiss Group for Clinical Cancer Research

Status and phase: Completed; Phase 3

Conditions: Gastric Cancer

Treatments: Drug: Taxotere-Cisplatin-5FU; Drug: Immediate surgery

Study type: Interventional

Funder types: Other

Identifiers

NCT00005060

SAKK 43/99

SWS-SAKK-43/99 (Other Identifier)

EU-99042

Details and patient eligibility

About

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one chemotherapy drug with surgery may kill more tumor cells. It is not yet known if chemotherapy followed by surgery is more effective than surgery followed by chemotherapy for stomach cancer.

PURPOSE: This randomized phase III trial is studying surgery followed by combination chemotherapy to see how well it works compared to combination chemotherapy followed by surgery in treating patients with locally advanced stomach cancer.

Full description

OBJECTIVES:

• Compare, by intention to treat analysis, feasibility and efficacy of 4 courses of docetaxel, cisplatin, and fluorouracil as preoperative or postoperative chemotherapy in patients with locally advanced operable gastric carcinoma.
• Evaluate the predictive values of some biological and molecular tumor parameters on response to chemotherapy, metastasis and survival in this patient population.

OUTLINE: This is a randomized, open label, multicenter study. Patients are stratified according to study center, tumor site (affecting the Z-line (cardia carcinoma Siewart II and III) vs rest of the stomach), and nodal status (positive vs negative). Patients are randomized to either preoperative chemotherapy followed by surgery (arm I) or surgery followed by postoperative chemotherapy (arm II).

• Arm I: Patients receive docetaxel IV over 1 hour followed by cisplatin IV over 4 hours on day 1, and fluorouracil IV continuously on days 1-14 every 3 weeks. Patients are evaluated after 2 courses and patients with progressive disease proceed to immediate surgery. Otherwise, treatment continues for a total of 4 courses in the absence of unacceptable toxicity or disease progression. Between 3-5 weeks following day 1 of the last course of chemotherapy, patients undergo gastric resection.
• Arm II: Patients undergo immediate gastric resection. Beginning 3-6 weeks after surgery, patients receive 4 courses of docetaxel, cisplatin, and fluorouracil as in arm I.

Quality of life is assessed before the first and third courses of chemotherapy, before and after surgery, and then at 1, 3, and 6 months.

Patients are followed every 3 months for 3 years, every 6 months for 2 years, and then annually thereafter.

PROJECTED ACCRUAL: Approximately 240 patients (120 per arm) will be accrued for this study.

Enrollment: 240 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed locally advanced gastric carcinoma that is considered operable

  • T3-4, Nx, M0 OR
  • Tx, N+, M0

• Lymph nodes considered positive by sonography should be at least 2 of the following:

  • Round
  • Echopoor
  • Sharp borders
  • At least 0.5 cm

• No distant metastases, including peritoneal carcinomatosis

  • CT scan and peritoneal lavage mandatory

PATIENT CHARACTERISTICS:

Age:

• 18 to 75

Performance status:

• 0-2

Life expectancy:

• Greater than 12 weeks

Hematopoietic:

• WBC at least 4,000/mm^3
• Platelet count at least 100,000/mm^3

Hepatic:

• Bilirubin normal
• AST or ALT no greater than 1.5 times upper limit of normal (ULN)
• Alkaline phosphatase no greater than 2.5 times ULN

Renal:

• Adequate renal function within limits to allow for treatment with cisplatin

Cardiovascular:

• No unstable cardiac disease requiring treatment
• No congestive heart failure or angina pectoris even if medically controlled
• No significant arrhythmias
• No myocardial infarction within past 6 months
• Ejection fraction greater than 50% on cardiac sonography or MUGA scan

Other:

• Not pregnant or nursing
• Fertile patients must use effective contraception
• No other prior malignancy except basal cell carcinoma of the skin or adequately treated carcinoma in situ of the cervix
• No grade 2 or greater peripheral neuropathy of any origin (e.g., alcohol, diabetic)
• No history of anaphylaxis
• No other serious concurrent illness or medical condition that would preclude study therapy
• No history of significant neurologic or psychiatric disorders (e.g., psychotic disorders, dementia, or seizures)

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• No concurrent biologic therapy for gastric carcinoma

Chemotherapy:

• No other concurrent chemotherapy for gastric carcinoma

Endocrine therapy:

• No concurrent endocrine therapy for gastric carcinoma

Radiotherapy:

• No concurrent radiotherapy for gastric carcinoma

Surgery:

• See Disease Characteristics

Other:

• At least 30 days since prior treatment in a clinical trial
• No other concurrent experimental drugs
• No other concurrent anticancer therapy

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: None (Open label)

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240 participants in 2 patient groups

Taxotere-Cisplatin-5FU preoperatively

Active Comparator group

Description:

TCF preoperatively

Treatment:

Drug: Taxotere-Cisplatin-5FU

Immediate surgery followed by TCF

Active Comparator group

Description:

Surgery followed by Taxotere-Cisplatin-5FU

Treatment:

Drug: Immediate surgery