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Spots Global Cancer Trial Database for Pembrolizumab in Treating Patients With Small Bowel Adenocarcinoma That is Metastatic or Locally Advanced and Cannot Be Removed by Surgery

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Trial Identification

Brief Title: Pembrolizumab in Treating Patients With Small Bowel Adenocarcinoma That is Metastatic or Locally Advanced and Cannot Be Removed by Surgery

Official Title: A Multicenter Phase II Study of Pembrolizumab (MK-3475) in Patients With Advanced Small Bowel Adenocarcinomas

Study ID: NCT02949219

Study Description

Brief Summary: This phase II trial studies how well pembrolizumab works in treating patients with small bowel adenocarcinoma that has spread to other places in the body or that cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, may interfere with the ability of tumor cells to grow and spread.

Detailed Description: PRIMARY OBJECTIVES: I. To determine whether pembrolizumab administered to small bowel adenocarcinoma (SBA) patients demonstrates antitumor activity as measured by the confirmed response rate. SECONDARY OBJECTIVES: I. To assess survival endpoints (overall survival \[OS\], progression free survival \[PFS\]), including stratified analysis by tumor site. II. To assess whether pembrolizumab is safe in SBA patients by assessing adverse events. TERTIARY OBJECTIVES: I. To determine whether PD-L1 expression, as measured by immunohistochemistry (IHC), or microsatellite instability (MSI) status is associated with the response rate overall. II. To determine if Bim levels in tumor-reactive CD11ahighPD-1+CD8+ peripheral blood T cells can objectively monitor responses to pembrolizumab and to determine if excessive release of soluble B7-H1 (soluble \[s\]PD-L1) by the tumor leads to Bim upregulation and treatment resistance in SBA. III. To determine if other tissue-based factors, such as total mutational burden, correlate with response to pembrolizumab. OUTLINE: Patients receive pembrolizumab intravenously (IV) over 30 minutes on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 3 months until disease progression, and then every 6 months for up to 5 years.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic Hospital, Phoenix, Arizona, United States

Mayo Clinic in Arizona, Scottsdale, Arizona, United States

MedStar Georgetown University Hospital, Washington, District of Columbia, United States

Mayo Clinic, Rochester, Minnesota, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

Rapid City Regional Hospital, Rapid City, South Dakota, United States

M D Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Robert McWilliams

Affiliation: Academic and Community Cancer Research United

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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