Multiple Myeloma Clinical Trial
Official title:
Early Onset Malignancies Initiative (EOMI): Molecular Profiling of Breast, Colon, Kidney, Liver, Multiple Myeloma, and Prostate Among Racially and Ethnically Diverse Populations
Verified date | February 2024 |
Source | National Cancer Institute (NCI) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This research trial studies how well biospecimen collection works in identifying genetic changes in patients with breast, prostate, colorectal, liver, or kidney cancer or multiple myeloma undergoing surgery. Studying samples collected during surgery may add to the understanding of cancer by looking for the genetic changes that cause early cancer onset in people of certain racial and ethnic groups.
Status | Suspended |
Enrollment | 2400 |
Est. completion date | December 31, 2026 |
Est. primary completion date | July 31, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients with either: - Histologically confirmed invasive carcinoma or multiple myeloma OR - Clinical diagnosis of carcinoma or multiple myeloma OR - Suspected clinical diagnosis of multiple myeloma - Patients with one of following tumor types and age ranges: - Breast cancer diagnosis at ages 18-45 - Colon cancer diagnosis at ages 18-55 - Kidney cancer at diagnosis at ages 18-50 (American Indian or Alaska Native [AIAN] and non-Hispanic Whites [NHW] only) - Liver cancer diagnosis at ages 18-55 - Prostate cancer diagnosis at ages 18-55 - Multiple myeloma diagnosis at ages 18-50 - Patients whose tumor specimen was collected or will be collected during one of the following routine procedures: - Surgery to remove cancer OR - Routine biopsy procedures performed to confirm a histologic diagnosis OR - Routine biopsy procedure performed to obtain additional tumor material for routine prognostic or predictive biomarkers OR - Routine procedure to place a vascular access device prior for systemic therapy - Patients who have received no therapy for their cancer other than surgery, irrespective of stage - Collection of specimens from living patients: - Ability to understand and willingness to sign a written informed consent document indicating their willingness to have their tissue or biologic fluid specimens used for research as outlined in this protocol - Collection of specimens from deceased patients: - Banked tissue samples and/or banked biologic fluid specimens of deceased patients may be used as long as all samples or specimens are properly de- identified prior to submission - Sites must use the Central Institutional Review Board for the National Cancer Institute (NCI CIRB). Exclusion Criteria: - Patients who do not meet criteria for an early onset malignancy - Prior systemic therapy or radiation therapy for their malignancy - Tumor does not meet quality metrics - Patient refused consent for use of tissue for research activities included in the Early Onset Malignancies Initiative - A diagnosis of a synchronous invasive malignancy - Patients with a history of invasive cancer or hematologic malignancy in preceding 5 years |
Country | Name | City | State |
---|---|---|---|
United States | National Cancer Institute Division of Cancer Prevention | Rockville | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Cancer Institute (NCI) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Acquisition of tissue, blood, and other biospecimens for research purposes | Will be performed. | Up to 3 years |
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