About clonoSEQ

A test that’s as determined as today’s cancer treatments

clonoSEQ is a blood or bone marrow test1 that measures your cancer at the deepest level currently available1-3, helping your doctor make more informed decisions about your care. clonoSEQ is FDA-cleared in bone marrow from patients with multiple myeloma or B-cell acute lymphoblastic leukemia (B-ALL) and in blood or bone marrow from patients with chronic lymphocytic leukemia (CLL). clonoSEQ is CLIA-validated in other types of blood cancer.

clonoSEQ is a blood or bone marrow test1 that measures your cancer at the deepest level currently available1-3, helping your doctor make more informed decisions about your care. clonoSEQ is FDA-cleared in bone marrow from patients with multiple myeloma or B-cell acute lymphoblastic leukemia (B-ALL) and in blood or bone marrow from patients with chronic lymphocytic leukemia (CLL). clonoSEQ is CLIA-validated in other types of blood cancer.

clonoSEQ is covered by Medicare and other major insurance providers

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.

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 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.

Here are some questions to help you start a conversation with your doctor.

  • Is MRD testing with clonoSEQ right for me?
  • I heard that clonoSEQ is the most sensitive MRD test available. Why does that matter for me?
  • What can MRD testing with clonoSEQ tell me about my cancer?
  • How will you incorporate MRD results from clonoSEQ into my treatment plan?
  • At what points during the treatment process should I have a clonoSEQ MRD test?

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:

  1. clonoSEQ®. [technical summary]. Seattle, WA. Adaptive Biotechnologies; 2020.
  2. Short N, et al. Am J Hematol. 2019;94(2):257-265.
  1. Martinez-Lopez J, et al. J Hematol Oncol. 2021;14(1):126.
  2. Data on file. Adaptive Biotechnologies. 2020.