About clonoSEQ
A test that’s as powerful as today’s cancer treatments
clonoSEQ is a blood or bone marrow test1 that measures your cancer at the deepest level currently available,1-3 helping your doctor make more informed decisions about your care. It is FDA-cleared in bone marrow and CLIA-validated in peripheral blood for multiple myeloma.
clonoSEQ is a blood or bone marrow test1 that measures your cancer at the deepest level currently available,1-3 helping your doctor make more informed decisions about your care. It is FDA-cleared in bone marrow and CLIA-validated in peripheral blood for multiple myeloma.
clonoSEQ helps your doctor tailor treatment to your needs
clonoSEQ uses next-generation sequencing technology, an advanced testing method that decodes your cancer’s genetic information, to look for unique cancer DNA sequences that serve as “barcodes.” After your diagnosis, clonoSEQ identifies and counts your cancer’s unique “barcodes.” During treatment and remission, clonoSEQ can tell you and your doctor if and how the number of “barcodes” has changed since your last MRD test.1
clonoSEQ is covered by Medicare and other major insurance providers
“Once I was told I was MRD-negative, the effects on my life have been huge. I no longer have to define myself as being a cancer patient. I’m no longer a cancer survivor. I’m a thriver.”
— Karen, a multiple myeloma patient who had clonoSEQ testing
clonoSEQ can find 1 cancer cell among a million healthy cells1*
What does 1 in a million mean to you? It means that you and your doctor know exactly where you are on your blood cancer journey. And when it comes to cancer, knowledge is power. By precisely tracking MRD both during and after treatment, you and your doctor can be more informed about your response to therapy—and can plan next steps accordingly.
*If sufficient sample material is provided.
clonoSEQ can identify residual disease that other tests miss4
Your doctor will likely order other tests—like flow tests or routine blood work—to
monitor your cancer. This is a good thing! It means your doctor is trying to gather as much
useful information as possible. To best understand how your cancer may be changing over
time, these tests can be paired with a highly sensitive MRD testing tool like clonoSEQ.
clonoSEQ detected MRD in
40-51%
of patients who were deemed
MRD-negative by a flow test4
Measure, then treat.
Treat, then measure.
Repeat throughout your journey.
There are several stages of treatment for multiple myeloma. Your doctor may want to check your MRD status after each stage, to see how effective treatment was before moving to the next stage.
Click through to see when your doctor may test you with clonoSEQ.
(1 of 4)
Initial diagnosis1
Identify cancer cell DNA
(Clonality (ID) Test)
The clonoSEQ Clonality (ID) Test provides a baseline. Because this test is done on the largest number of cancer cells, it helps clonoSEQ know which cells to look for in later tests.
(2 of 4)
After induction therapy5
This first part of your treatment usually includes targeted therapy and corticosteroids. Your doctor may test your MRD to see how well you have responded, prior to transplant (if transplant is part of your care plan).
(3 of 4)
After stem cell transplant
(if you receive a transplant)5
Healthy stem cells replace the stem cells in your bone marrow that induction therapy destroyed. Your doctor may test to assess your disease status at this time.
(4 of 4)
During maintenance therapy and beyond5
A low dose of a targeted therapy given over a long period of time may help maintain or even improve the good results of prior treatments. Guidelines suggest clonoSEQ can be used to monitor MRD long term in patients with sustained MRD negativity during or after maintenance therapy. Your clonoSEQ MRD status can help inform ongoing discussions concerning next steps.
If you are not planning for a transplant or perhaps aren’t eligible to receive one, your doctor may use clonoSEQ at initial diagnosis, then at various time points for added security and insight into your health. Regular testing with clonoSEQ can also help you know if your cancer has returned, so your doctor can take appropriate next steps.
This page is intended for a US-based audience.
clonoSEQ® is available as an FDA-cleared in vitro diagnostic (IVD) test service provided by Adaptive Biotechnologies to detect measurable residual disease (MRD) in bone marrow from patients with multiple myeloma or B-cell acute lymphoblastic leukemia (B-ALL) and blood or bone marrow from patients with chronic lymphocytic leukemia (CLL). Additionally, clonoSEQ is available for use in other lymphoid cancers and specimen types as a CLIA-validated laboratory developed test (LDT). To review the FDA-cleared uses of clonoSEQ, visit clonoSEQ.com/technical-summary.
References:
- clonoSEQ®. [technical summary]. Seattle, WA: Adaptive Biotechnologies; 2020.
- Short NJ, et al. Am J Hematol. 2019;94:257-265.
- Martinez-Lopez J, et al. J Hematol Oncol. 2021;14(1):126.
- Pulsipher M, et al. Blood Cancer Discov. 2022;3(1):66-81.
- Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Multiple Myeloma V.1.2022. © National Comprehensive Cancer Network, Inc. 2021. All rights reserved. Accessed January 16, 2024. To view the most recent and complete version of the guideline, go online to NCCN.org. NCCN makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.