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Gastrointestinal Cancer

Ramucirumab for Gastric, Esophageal and Gastroesophageal Cancer (7575)
Randomized, Placebo-Controlled, Double-Blind Phase 2 Study of mFOLFOX6 Chemotherapy Plus Ramucirumab Drug Product(IMC-1121B) Versus mFOLFOX6 Plus Placebo for Advanced Adenocarcinoma of the Esophagus, Gastroesophageal Junction or Stomach
Status Conditions Phase Study ID
Closed Stomach Cancer
Esophageal Cancer
Phase II NCT01246960
Summary

The purpose of this study is to determine whether ramucirumab when used in conjunction with chemotherapy treatment can help patients with stomach, esophagus and gastroesophageal cancer.


Investigator
Andrew Coveler, MD
Location    
Seattle Cancer Care Alliance 800-804-8824  
Multicare Health System, Tacoma WA 253-403-5265  
Skagit Valley Hospital, Mt. Vernon WA 360-424-2687  
Wenatchee Valley Medical Center, Wenatchee WA 509-665-5800 x5122  
Columbia Basin Hematology & Oncology, Kennewick, WA 509-783-4637  
Eligibility Criteria (must meet the following to participate in this study)
  • Histologic or cytologic confirmation of adenocarcinoma of the esophagus, gastroesophageal junction (GEJ) or stomach
  • Metastatic or locally advanced, unresectable disease at time of study entry
  • Provided signed informed consent and is amenable to compliance with protocol schedules and testing
  • Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-1 at study entry
  • Adequate renal, hematological and hepatic function
  • Measurable or non-measurable disease at the time of study entry
  • Resolution to Grade less than or equal to 1 by the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE), Version 4.0, of all clinically significant toxic effects of prior locoregional therapy, surgery, or other anticancer therapy, except where otherwise mentioned in the eligibility criteria
  • Eligible patients of reproductive potential (both sexes) must agree to use adequate contraceptive methods (hormonal or barrier methods) during the study period and at least 12 weeks after the last dose of study therapy
  • Life expectancy of greater than or equal to 3 months
  • Willingness to provide blood and tissue samples for research purposes Submission of tumor specimen is mandatory for participation in this study, if a histologic, paraffin-embedded specimen exists (either from a surgical resection or biopsy); submission of paraffin block or a minimum of 8 unstained slides is required if sufficient sample. NOTE: If insufficient additional tissue exists (that is, all tissue has been utilized for prior diagnostic purposes), participation in the study is allowable without the requirement for an additional biopsy; this situation must be discussed with the study principal investigator and/or the ImClone medical monitor or designee
Exclusions (conditions that would prevent participation in this study)
  • The patient has received prior first-line systemic therapy for advanced/unresectable and/or metastatic disease (prior adjuvant or neo- adjuvant therapy is permitted)
  • Previous or concurrent malignancy except for basal or squamous cell skin cancer and/or in situ carcinoma of the cervix, or other solid tumors treated curatively and without evidence of recurrence for at least 3 years prior to study entry
  • Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, and in the judgment of the investigator would make the patient ineligible for entry into this study
  • The patient is receiving chronic therapy with nonsteroidal anti- inflammatory agents (NSAIDs; for example, indomethacin, ibuprofen, naproxen, or similar agents) or other antiplatelet agents (for example, clopidogrel, ticlopidine, dipyridamole, anagrelide). Aspirin use at doses up to 325 mg/day is permitted
  • The patient has significant third-space fluid retention (for example, ascites or pleural effusion), and is not amenable for required repeated drainage
  • The patient is pregnant or breastfeeding
  • Uncontrolled intercurrent illness including, but not limited to, active or uncontrolled clinically serious infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled thromboembolic or hemorrhagic disorder, psychiatric illness/social situations, or other co-morbid systemic illnesses or other severe concurrent disease
  • Immunocompromised patients including patients known to be HIV positive.
  • Progressive disease less than or equal to 12 months of completing platinum or 5-FU treatment, including capecitabine, if given previously in the perioperative (adjuvant or neoadjuvant) setting
  • Current or recent (within 28 days prior to randomization) treatment with an investigational drug that has not received regulatory approval for any indication at the time of study entry, or participation in another interventional clinical trial. Patients participating in surveys or observational studies are eligible to participate in this study.
  • Are currently enrolled in, or discontinued from, a clinical trial involving ramucirumab DP, or concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study
  • Received prior therapy with an antiangiogenic agent (including but not limited to bevacizumab, sunitinib or sorafenib)
  • Major surgical procedure or significant traumatic injury greater less 28 days prior to registration, or anticipation of need for elective or planned major surgical procedure during the course of the study. Subcutaneous venous access device placement within 7 days prior to randomization
  • Clinically significant peripheral neuropathy at the time of registration
  • Known central nervous system metastases that are symptomatic or untreated
  • New York Heart Association (NYHA) classification III-IV congestive heart failure
  • Greater than normal risk of bleeding or coagulopathy in the absence of therapeutic anticoagulation; Grade 3/4 gastrointestinal bleeding within 3 months prior to registration; active bleeding (that is, within 14 days prior to first dose of study therapy); or pathological condition present that carries a high risk of bleeding (for example, tumor involving major vessels or known varices)
  • Patient has experienced any arterial thromboembolic events, including but not limited to myocardial infarction, stroke, transient ischemic attack (TIA), cerebrovascular accident, or unstable angina, less than or equal to 6 months prior to registration
  • Clinically significant vascular disease (for example, aortic aneurysm, aortic dissection) for which more than minimal intervention is being administered or planned
  • History of hypertensive crisis or hypertensive encephalopathy or current poorly-controlled hypertension despite standard medical management.
  • History of abdominal fistula, gastrointestinal perforation, or intraabdominal abscess great less than 6 months prior to registration.
  • Known hypersensitivity to any of the treatment components of mFOLFOX6 or ramucirumab DP
Last Updated
December 21, 2012
See this trial at ClinicalTrials.gov
Access protocol and consent forms at Fred Hutchinson Cancer Research Center
Disclaimer: We update this information regularly. However, what you read today may not be completely up to date.

Please remember:
  • Talk to your health care providers first before making decisions about your health care.
  • Whether you are eligible for a research study depends on many things. There are specific requirements to be in research studies. These requirements are different for each study.