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NCT01505400
Integrated Molecular Profiling in Advanced Cancers Trial
Conditions: Breast Cancer, Non-small Cell Lung Cancer, Colorectal Cancer, Genitourinary Cancer, Pancreatobiliary Gastrointestinal Cancer, Upper Aerodigestive Tract Cancer, Gynecological Cancers, Melanoma Cancers, Rare Cancers, Unknown Primary Cancers
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 3026
Sponsor: University Health Network, Toronto
Location: Princess Margaret Hospital Toronto Ontario
Summary
Substantial progress has been made in the treatment of cancer through the use of targeted therapies, but what works for one patient might not work for another patient. Certain drugs are now being developed that target specific molecules in the body that are believed to be part of the disease.
Biomarkers are specific characteristics of the cancer that may help provide prognostic information (i.e. how well patients will be regardless of the treatments given) or help predict sensitivity or resistance to a specific treatment.
The study will collect archival tumor samples (previously collected biopsy or surgical tumor samples) to provide biomarker data about a patient's cancer, in order to help their physicians to identify which clinical trials of molecularly targeted therapies may be most appropriate for the patient in the future.
Eligibility Criteria
Inclusion Criteria:
* Patients with histological confirmation of advanced breast, non-small cell lung, colorectal, genitourinary, pancreatobiliary gastrointestinal, upper aerodigestive tract, gynecological, melanoma, unknown primary, and rare carcinomas who are candidates for systemic therapy, as well as patients who are phase I trial candidates.
* Patient must be ≥ 18 years old.
* Patient's ECOG performance status equal to 0 or 1.
* All patients must have signed and dated an informed consent form.
* All patients must have sufficient archived tumor tissue for molecular profiling.
Exclusion Criteria:
* None
Source: ClinicalTrials.gov (NCT01505400). StuddyBuddy aggregates publicly available trial information.