Molecular Analysis for Therapy Choice (MATCH)

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: lymphoma | neoplasm | myeloma
  • Age: Between 18 - 100 Years
  • Gender: Male or Female

Inclusion Criteria
Women of childbearing potential must have a negative serum pregnancy test within 2 weeks prior to registration
Patients must have histologically documented solid tumors or histologically confirmed diagnosis of lymphoma that has progressed following at least one line of standard systemic therapy and/or for whose disease no standard treatment exists that has been shown to prolong survival
Patients must have measurable disease
Patients must have tumor amenable to image guided or direct vision biopsy and be willing and able to undergo a tumor biopsy for molecular profiling; biopsy must not be considered to be more than minimal risk to the patient
Patient must not require the use of full dose coumarin-derivative anticoagulants such as warfarin; low molecular weight heparin is permitted for prophylactic or therapeutic use; stopping the anticoagulation for biopsy should be per site standard operating procedure (SOP)
Patients must have Eastern Cooperative Oncology Group (ECOG) performance status == 4 weeks prior to registration to Step 0
Patients must have discontinued steroids >= 1 week prior to registration to Step 0; patients with glioblastoma (GBM) must have been on stable dose of steroids, or be off steroids, for one week prior to registration to Step 0
Exclusion Criteria
Patients that are pregnant or breast feeding are excluded

Recruitment Status


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