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Spots Global Cancer Trial Database for Treatment Based on Molecular Profiling Diagnosis Carcinoma of Unknown Primary Site

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Treatment Based on Molecular Profiling Diagnosis Carcinoma of Unknown Primary Site

Official Title: A Phase II Study of Chemotherapy Treatment Based on Molecular Profiling Diagnosis for Patients With Carcinoma of Unknown Primary Site

Study ID: NCT00737243

Conditions

Carcinoma

Study Description

Brief Summary: This is a non-randomized Phase II study. Patients determined at initial diagnosis to have a carcinoma of unknown primary site (CUP) will have their treatment selected with the use of a molecular profiling assay. The assay will be performed on paraffin-embedded tumor tissue from a biopsy specimen. Patients given specific diagnoses (e.g., lung, pancreas, colon, breast, renal cell, prostate and ovarian cancer) will receive treatment regimens of proven activity. If no specific diagnosis is made with the molecular profiling assay, empiric chemotherapy with paclitaxel, carboplatin, bevacizumab and erlotinib will be administered.

Detailed Description: The primary objective of the study is evaluate the impact of the molecular assay prediction on the efficacy of therapy for patients with carcinoma of unknown primary site (CUP). Investigators will use tumor profiling results to direct standard, site-specific first-line therapy for patients with CUP.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Oncology Specialties (Clearview Cancer Institute), Huntsville, Alabama, United States

Florida Cancer Specialists, Fort Myers, Florida, United States

Integrated Community Oncology Network, Jacksonville, Florida, United States

Watson Clinic Center for Cancer Care and Research, Lakeland, Florida, United States

Florida Hospital Cancer Institute, Orlando, Florida, United States

Northeast Georgia Medical Center, Gainesville, Georgia, United States

Wellstar Cancer Research, Marietta, Georgia, United States

Oncology Hematology Associates of SW Indiana, Evansville, Indiana, United States

Baptist Hospital East, Louisville, Kentucky, United States

Hematology Oncology Clinic, LLP, Baton Rouge, Louisiana, United States

Center for Cancer and Blood Disorders, Bethesda, Maryland, United States

Grand Rapids Clinical Oncology Program, Grand Rapids, Michigan, United States

Jackson Oncology Associates, Jackson, Mississippi, United States

Nebraska Methodist Cancer Center, Omaha, Nebraska, United States

Hematology Oncology Associates of Northern NJ, Morristown, New Jersey, United States

Oncology Hematology Care, Cincinnati, Ohio, United States

Spartanburg Regional Medical Center, Spartanburg, South Carolina, United States

Chattanooga Oncology Hematology Associates, Chattanooga, Tennessee, United States

Tennessee Oncology, PLLC, Nashville, Tennessee, United States

Center for Cancer and Blood Disorders, Ft. Worth, Texas, United States

Virginia Cancer Institute, Richmond, Virginia, United States

Contact Details

Name: John D Hainsworth, M.D.

Affiliation: SCRI Development Innovations, LLC

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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