Clinical MRD Patient Cases

This site is designed to enable clinicians to access and share de-identified summaries of real patient cases for which measurable residual disease (MRD) testing has been utilized in clinical practice. These cases have been collected from current clonoSEQ users to illustrate the ways in which clonoSEQ MRD testing is being incorporated in the day-to-day management of myeloma and acute lymphoblastic leukemia (ALL) patients.

Scroll down to review the case library, or use the filters below to search for a case with specific characteristics. To submit a case for one of your own patients, click here.

Patient Case Results:

* This patient case includes examples of clonoSEQ MRD testing in blood. Blood-based MRD testing for patients with acute lymphoblastic leukemia is available as a CLIA-regulated laboratory developed test (LDT) service provided by Adaptive Biotechnologies. This use of clonoSEQ has not been approved or cleared by the FDA.

clonoSEQ is available as an FDA-cleared in vitro diagnostic (IVD) test service provided by Adaptive Biotechnologies for use in B-cell acute lymphoblastic leukemia and multiple myeloma patients to detect and monitor measurable residual disease (MRD) in bone marrow samples. clonoSEQ is also available for use in other lymphoid cancers as a CLIA-regulated laboratory developed test (LDT) service provided by Adaptive Biotechnologies. For important information about the FDA-cleared uses of clonoSEQ including test limitations, please review the Technical Summary, clonoseq.com/technical-summary.

Submit a Patient Case

Do you have an MRD case from your own practice that you would like to share?
Fill out an online case form and submit for review by Adaptive Medical Affairs, or download the form and email a completed version to casestudies@adaptivebiotech.com.