Study to Explore the Mechanism of Acquired Immune Escape In Participants With Metastatic Cancer Progressing on CPI Therapy
- Conditions
- Neoplasms
- Interventions
- Procedure: Biopsy
- Registration Number
- NCT03333655
- Lead Sponsor
- Hoffmann-La Roche
- Brief Summary
The purpose of this study is to identify mechanisms associated with acquired immune escape by comparing baseline and at-progression tissue samples from participants who derive clinical benefit from CPI treatment of metastatic cancer or hematologic malignancies.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 15
- Response assessment of complete response (CR), partial response (PR), or long-term stable disease (SD) for >6 months with a cancer immunotherapy treatment for metastatic cancer or hematologic malignancies either through a marketed CPI or through participation in a Roche/Genentech CPI clinical trial.
- Availability of tissue sample.
- Pregnant, lactating, or intending to become pregnant during the study.
- Participants receiving CPI treatment as part of a non-Roche/Genentech clinical trial.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Checkpoint Inhibitor Therapy Biopsy Pre-treatment (archival) and at progression biopsy for participants with a demonstrated clinical benefit on CPI therapy will be asked to participate in the study. In addition, retrospective enrollment of patients who progressed on CPI therapy after documented response and for whom an at-progression biopsy is available, is also possible.
- Primary Outcome Measures
Name Time Method Number of Gene Alterations in at-Progression Biopsy of Patricipants with Acquired Immune Escape Day 1 Number of Gene Alterations Will Be Evaluated Using NGS Approaches by Comparing At-Progression Biopsy with Pre-Treatment Biopsy
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (11)
Dana-Farber Cancer Institute
๐บ๐ธBoston, Massachusetts, United States
UCSF Comp Canc Ctr
๐บ๐ธSan Francisco, California, United States
Washington University School of Medicine; Dept of Medicine/Div of Medical Oncology
๐บ๐ธSaint Louis, Missouri, United States
Herbert Irving Comprehensive Cancer Center; Herbert Irving Pavillion
๐บ๐ธNew York, New York, United States
Hospital Univ Vall d'Hebron; Servicio de Oncologia
๐ช๐ธBarcelona, Spain
Clinica Universitaria de Navarra; Servicio de oncologรญa
๐ช๐ธPamplona, Navarra, Spain
Sarah Cannon Cancer Center
๐บ๐ธArrington, Tennessee, United States
Institut Universitaire du Cancer - Oncopole Toulouse (IUCT-O)
๐ซ๐ทToulouse, France
Barts Hospital; Institute of Cancer
๐ฌ๐งLondon, United Kingdom
Seoul National University Hospital; Department of Oncology
๐ฐ๐ทSeoul, Korea, Republic of
Asan Medical Center, Uni Ulsan Collegemedicine; Dept.Internal Medicine / Divisionhematology/Oncology
๐ฐ๐ทSeoul, Korea, Republic of