Vaccine Therapy Plus Chemotherapy in Treating Patients With Metastatic or Locally Recurrent Stomach Cancer or Esophageal Cancer

OBJECTIVES: I. Determine a safe and immunogenic combination of G17DT with cisplatin and
fluorouracil in patients with chemotherapy-naive metastatic or locally recurrent gastric or
gastroesophageal cancer. II. Determine the safety profile and tolerability of this regimen
in these patients. III. Determine the tumor response rate, disease stabilization, best
overall response, time to progression, time to treatment failure, and overall survival in
patients treated with this regimen. IV. Determine the correlation of immunological response
with clinical efficacy and benefit in patients treated with this regimen. V. Determine the
pharmacokinetics and pharmacodynamics of this regimen in these patients.

OUTLINE: This is a multicenter study. Patients are assigned to one of four treatment
regimens. Regimen A: Patients receive high-dose G17DT intramuscularly (IM) on days 7, 35,
and 63. Patients also receive cisplatin IV over 1-3 hours on day 1 followed by fluorouracil
IV continuously over days 1-5 every 4 weeks in the absence of disease progression or
unacceptable toxicity. If inadequate immune response is seen on Regimen A, subsequent
patients are treated on Regimen B. If unacceptable toxicity is seen on Regimen A, subsequent
patients are treated on Regimen C. If inadequate immune response and unacceptable toxicity
are seen on Regimen A, or if unacceptable toxicity is seen on Regimen B or inadequate immune
response is seen on Regimen C, then subsequent patients are treated on Regimen D. Regimen B:
Patients receive high-dose G17DT IM on days 1, 28, and 56. Patients also receive cisplatin
IV over 1-3 hours on day 35 followed by fluorouracil IV continuously over days 35-39 every
four weeks in the absence of disease progression or unacceptable toxicity. Regimen C:
Patients receive low-dose G17DT IM on days 7, 35, and 63 with chemotherapy as in regimen A.
Regimen D: Patients receive low-dose G17DT IM on days 1, 28, and 56 with chemotherapy as in
regimen B. Quality of life is assessed at baseline, on day 7, every 2 weeks for 10 weeks,
and then every 4 weeks thereafter.

PROJECTED ACCRUAL: A total of 15-75 patients will be accrued for this study within 5-30
months.

Inclusion Criteria:

- Signed informed consent.

- Gastric adenocarcinoma, including adenocarcinoma of the esophagogastric junction,
histologically proven.

- Measureable metastatic disease.

- Male or female subjects, age 18 years and older.

- Karnofsky performance status score equal to or greater than 70.

- Life expectancy of at least 3 months.

- Subjects must be chemotherapy naïve.

- At least 6 weeks from prior curative radiotherapy and 3 weeks from surgery.

- Adequate hematological and coagulation parameters: hemoglobin>9.5 g/dL; white blood
cell count>3x10^9/L, platelets> 100x10^9/L; international normalized ratio of
prothrombin time <1.2, and activated partial thromboplastin time no more than 5
seconds above normal limits.

- Adequate clinical chemistry parameters: creatinine<1.5mg/dL; total
bilirubin<1.5mg/dL; and aspartate aminotransferase and alanine aminotransferase <2.5x
upper normal levels.

- Able to comply with scheduled follow-up and with management of toxicity.

- Use contraceptive measures, if sexually active

Exclusion Criteria:

- Previous or current malignancies other than gastric adenocarcinoma, with the
exception of adequately treated in situ carcinoma of the cervix, uteri, or
nonmelanoma skin cancer

- Female subjects who are pregnant or nursing

- Female subjects with reproductive potential refusing a pregnancy test

- Any previous palliative chemotherapy, adjuvant or neoadjuvant chemotherapy, or
investigational drug

- Any prior anticancer immunotherapy

- Immunodeficiency

- Bone marrow transplantation within 1 year

- Symptomatic peripheral neuropathy > Grade 2 NCI-CTC, Version 2.0 criteria

- Severe hearing disorder > Grade 2 NCI-CTC, Version 2.0 criteria

- Known dihydropyrimidine dehydrogenase deficiency

- Any other sever condition as defined by the following: unstable cardiac disease
despite treatment; myocardial infarction within 6 months before study entry; history
of significant neurologic or psychiatric disorders including dementia or seizures;
active uncontrolled infection; active disseminated intravascular coagulation; or any
other serious underlying medical conditions that could impair the ability of the
subject to participate in the study

- Subjects who have previously demonstrated hypersensitivity to diphtheria toxoid

- Subjects who require chronic administration of corticosteroids

- Use in the past 30 days or concomitant use of immunosuppressants

- Use in the past 14 days or chronic concomitant use of proton pump inhibitors

- Subjects who have a history of hypercalcemia

- Subjects who cannot be regularly followed up for psychological, social, familial, or
geographic reasons

- Subjects with expected noncompliance to toxicity management