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Phase 2 N=26 Treatment

Pharmacogenomically Selected Treatment for Gastric and Gastroesophageal Junction (GEJ) Tumors

Stomach Neoplasms · Esophageal Neoplasms

Enrolled (actual)
26
Serious AEs
0.0%
Results posted
Feb 2015
Primary outcome: Primary: Overall Response Rate (ORR) — 39.1 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
5-fluorouracil (Drug); Oxaliplatin (Drug); Leucovorin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Vanderbilt University
Primary completion
Aug 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Response Rate (ORR)
39.1
SECONDARY
Overall Survival
11.4
SECONDARY
Progression-free Survival (PFS)
6.2
SECONDARY
Disease Control Rate (DCR)
95.7
SECONDARY
Tumor Specific Changes That May Alter Treatment Outcomes
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)
0; 9; 0
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)
0; 9; 0
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)
0; 9; 0
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)
0; 9; 0
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)
0; 9; 0
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)
0; 9; 0
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)
0; 9; 0
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)
1; 6; 4
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)
1; 6; 4
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)
1; 6; 4
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)
1; 6; 4
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)
1; 6; 4
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)
1; 6; 4
SECONDARY
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)
1; 6; 4

Summary

This study is for patients who have stomach cancer or cancer of the lower part of the esophagus that has spread to other organs. There are many different chemotherapy treatments for this type of cancer. At the present time, there is no general agreement on the way to choose the most beneficial therapy for an individual patient. Patients with different genetic backgrounds may respond differently to the same chemotherapy treatments. In this study the investigators will use a certain genetic difference in an important gene (thymidylate synthase or TS gene) to see whether treating patients who have a particular type of that gene will respond better to a standard chemotherapy regimen. The investigators are hoping that by treating patients according to their genes, that they may respond to treatment of their cancer better and it will help the investigators choose cancer treatments better in the future.

Eligibility Criteria

Inclusion Criteria

  • Patients must have histologically or cytologically confirmed adenocarcinoma of the stomach or gastroesophageal junction.
  • Patients must have measurable disease.
  • No prior therapy for metastatic disease. Prior neo-adjuvant or adjuvant therapy is permitted if the disease free interval has been longer than 6 months.
  • Age ≥18 years.
  • Life expectancy of greater than 3 months.
  • ECOG (Eastern Cooperative Oncology Group) performance status greater than 2 (Karnofsky greater than 60%).
  • Patients must have normal organ and marrow function.
  • Not pregnant. Not breast feeding.
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

  • Patients may not be receiving any other chemotherapy agents.
  • Patients with known active brain metastases. Patients with treated brain metastases are permitted if stable off steroids for at least 30 days.
  • History of allergic reactions to 5-FU or oxaliplatin.
  • Uncontrolled intercurrent illness.
  • Patients with immune deficiency.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00515216). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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