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

Pharmacogenomically Selected Treatment for Gastric and Gastroesophageal (GEJ) Tumors: A Phase II Study

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.

Study Overview

• Status: Completed
• Conditions: Stomach Neoplasms; Esophageal Neoplasms
• Intervention / Treatment: Drug: Oxaliplatin; Drug: Leucovorin; Drug: 5-fluorouracil

Detailed Description

Gastric and gastroesophageal junction (GEJ) cancers are a leading cause of cancer mortality. Despite the development of newer chemotherapies, the response rates and median survival in patients with these tumors has remained essentially stagnant. Defining host and molecular/biologic tumor characteristics to customize treatment may lead to improved survival outcomes. Retrospective studies have identified genetic markers that predict treatment outcome. However, there have been no prospective studies in gastric and GEJ cancer evaluating the clinical utility of these genetic factors. We hypothesize that genomically based treatment will improve the expected response rate in patients with gastric and GEJ cancers. We propose a prospective, multi-institutional Phase II clinical trial testing a germline polymorphism in the thymidylate synthase (TS) gene, the number of tandem repeats in the TS enhancer region (TSER) as a treatment selection marker. The polymorphic variant conferring three tandem repeats (TSER*3) has been associated with 5-FU resistance due to high tumor TS expression in comparison to the TSER*2 variant (two tandem repeats). The TSER*3 polymorphism is common (allelic frequency of 0.5-0.8). In the proposed study, we will prospectively genotype patients with gastric and GEJ cancers. Patients who are expected to be 5-FU sensitive (carrying a TSER*2 allele) will receive a 5-FU containing regimen (5-FU, leucovorin, oxaliplatin). Patients who are expected to be 5-FU resistant (homozygous for TSER*3) will not be included in the study. In completing this study, we will determine whether treatment selection based on germline TSER polymorphism status improves the response rate in patients with metastatic gastric and GEJ tumors. Additional correlative studies are proposed to identify confounding factors that may alter the expected outcomes of this treatment approach.

• Study Type: Interventional
• Enrollment (Actual): 26
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • Alabama
    • Birmingham, Alabama, United States, 35294
      • University of Alabama at Birmingham
  • Missouri
    • St. Louis, Missouri, United States, 63110
      • Washington University School of Medicine
  • North Carolina
    • Chapel Hill, North Carolina, United States, 27599
      • University of North Carolina
  • Tennessee
    • Nashville, Tennessee, United States, 37232
      • Vanderbilt University Medical Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Oxaliplatin/Leucovorin/5-FU; "Good risk" patients with the TSER*2/*2 or *2/*3 genotype or low TS expression genotype received treatment of oxaliplatin, leucovorin given over 2 hours along with 5-FU given as intravenous push followed by 5-FU given as intravenous infusion of 46 hours. This treatment was repeated every 2 weeks.	Drug: Oxaliplatin; Other Names: Eloxatin; Drug: Leucovorin; Other Names: Wellcovorin; citrovorum factor; folinic acid; 5-formyl tetrahydrofolate; Drug: 5-fluorouracil; Other Names: 5-FU; Fluorouracil

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Overall Response Rate (ORR)	ORR = complete response + partial response; Complete response - disappearance of all target and non-target lesions; Partial response - at least a 30% decrease in the sum of the longest diameter of target lesions, taking as reference the baseline sum longest diameter	2 years

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Overall Survival		4 years
Progression-free Survival (PFS)	Progressive disease - at least a 20% increase in the sum of the longest diameter (LD) of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions	4 years
Disease Control Rate (DCR)	DCR - complete response, partial response, and stable disease; Complete response - disappearance of all target and non-target lesions; Partial response - at least a 30% decrease in the sum of the longest diameter of target lesions, taking as reference the baseline sum longest diameter; Stable disease - neither sufficient shrinkage to qualify for partial response not sufficient increase to qualify for progressive disease	2 years
Tumor Specific Changes That May Alter Treatment Outcomes		4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)	This outcome looks at what genotypes of the TYMS 5'-UTR TSER + G>C (rs34743033) gene had a partial tumor response.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)	This outcome looks at what genotypes of the TYMS 3'-UTR 1494delTTAAAG(6 bp) (rs34489327) gene had a partial tumor response.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)	This outcome looks at what genotypes of the ERCC1 c.354C>T (rs11615) gene had a partial tumor response.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)	This outcome looks at what genotypes of the ERCC2 c.2251A>C (rs13181) gene had a partial response.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)	This outcome looks at what genotypes of the GSTP1 c.313A>G (rs1695) gene had a partial response.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)	This outcome looks at what genotypes of the XRCC1 c.1196G>A (rs25487) gene had a partial response.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Partial Response)	This outcome looks at what genotypes of the MDR1 c.3435C>T (rs1045642) gene had a partial response.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)	This outcome looks at what genotypes of the TYMS 5'-UTR TSER + G>C (rs34743033) gene had stable disease.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)	This outcome looks at what genotypes of the TYMS 3'-UTR 1494delTTAAAG(6 bp) (rs34489327) gene had stable disease.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)	This outcome looks at what genotypes of the ERCC1 c.354C>T (rs11615) gene had stable disease.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)	This outcome looks at what genotypes of the ERCC2 c.2251A>C (rs13181) gene had stable disease.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)	This outcome looks at what genotypes of the GSTP1 c.313A>G (rs1695) gene had stable disease.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)	This outcome looks at what genotypes of the XRCC1 c.1196G>A (rs25487) gene had stable disease.	4 years
Genetic Polymorphisms That May Alter Treatment Outcomes (Stable Disease)	This outcome looks at what genotypes of the MDR1 c.3435C>T (rs1045642) gene had stable disease.	4 years

Collaborators and Investigators

• Sponsor: Vanderbilt University
• Collaborators: National Cancer Institute (NCI); Washington University School of Medicine; University of Alabama at Birmingham; University of North Carolina
• Investigators: Principal Investigator: Albert C. Lockhart, M.D., Washington University School of Medicine; Principal Investigator: Laura Goff, M.D., Vanderbilt University Medical Center; Principal Investigator: Richard Goldberg, M.D., University of North Carolina; Principal Investigator: James Posey, M.D., University of Alabama at Birmingham

Publications and helpful links

General Publications

• Goff LW, Thakkar N, Du L, Chan E, Tan BR, Cardin DB, McLeod HL, Berlin JD, Zehnbauer B, Fournier C, Picus J, Wang-Gillam A, Lee W, Lockhart AC. Thymidylate synthase genotype-directed chemotherapy for patients with gastric and gastroesophageal junction cancers. PLoS One. 2014 Sep 18;9(9):e107424. doi: 10.1371/journal.pone.0107424. eCollection 2014.

Helpful Links

• Vanderbilt-Ingram Cancer Center
• Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine
• UNC Lineberger Comprehensive Cancer Center
• University of Alabama at Birmingham . Comprehensive Cancer Center

Study record dates

Study Major Dates

• Study Start: August 1, 2007
• Primary Completion (Actual): August 1, 2011
• Study Completion (Actual): November 1, 2013

Study Registration Dates

• First Submitted: August 9, 2007
• First Submitted That Met QC Criteria: August 10, 2007
• First Posted (Estimate): August 13, 2007

Study Record Updates

• Last Update Posted (Estimate): January 7, 2016
• Last Update Submitted That Met QC Criteria: December 8, 2015
• Last Verified: December 1, 2015

More Information

Terms related to this study

• Keywords: Gastric cancer; Metastatic; Phase II; FOLFOX; Pharmacogenomic; Gastroesophageal cancer; Thymidylate synthase
• Additional Relevant MeSH Terms: Digestive System Diseases; Neoplasms by Site; Gastrointestinal Neoplasms; Digestive System Neoplasms; Gastrointestinal Diseases; Stomach Diseases; Head and Neck Neoplasms; Esophageal Diseases; Neoplasms; Stomach Neoplasms; Esophageal Neoplasms; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Antimetabolites, Antineoplastic; Antimetabolites; Antineoplastic Agents; Immunosuppressive Agents; Immunologic Factors; Protective Agents; Micronutrients; Vitamins; Antidotes; Vitamin B Complex; Fluorouracil; Oxaliplatin; Leucovorin; Levoleucovorin; Tetrahydrofolates; Formyltetrahydrofolates
• Other Study ID Numbers: 070433; R21CA123881 (U.S. NIH Grant/Contract)