About clonoSEQ

A test that keeps up with today’s cancer treatments

clonoSEQ is a blood or bone marrow test1 that measures your child’s cancer at the deepest level currently available1-3, helping your child’s doctor make more informed decisions about their care. It is FDA-cleared in bone marrow and CLIA-validated in peripheral blood for B-cell acute lymphoblastic leukemia (B-ALL).

clonoSEQ is a blood or bone marrow test1 that measures your child’s cancer at the deepest level currently available1-3, helping your child’s doctor make more informed decisions about their care. It is FDA-cleared in bone marrow and CLIA-validated in peripheral blood for B-cell acute lymphoblastic leukemia (B-ALL).

clonoSEQ is covered by Medicare and other major insurance providers

What does 1 in a million mean? It means that you know exactly where your child is in their journey. By precisely tracking MRD both during and after treatment, you and your child’s doctor can be more informed about their 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 child’s doctor will likely order other tests to monitor your child’s cancer. This is a good thing! It means they’re trying to gather as much information as possible. To best understand how your child’s cancer may be changing over time, these tests can be paired with highly sensitive MRD testing tools like clonoSEQ.2-7

clonoSEQ detected MRD in

of patients who were deemed
MRD-negative by other testing5

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

  • I would like you to order clonoSEQ so we can keep a close eye on my child’s cancer. How do we get started?
  • I heard that clonoSEQ can identify 1 cancer cell out of a million cells with sufficient sample. Why does that matter for my child?
  • What can MRD testing with clonoSEQ tell me about my child’s cancer?
  • How can we get clonoSEQ MRD testing incorporated into my child’s care plan?
  • At what points during the treatment process should my child have a clonoSEQ MRD test?
  • How can we ensure coverage for clonoSEQ testing?

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 NJ, et al. Am J Hematol. 2019;94:257-265.
  3. Martinez-Lopez J, et al. J Hematol Oncol. 2021;14(1):126.
  4. Short N, et al. Blood Adv. 2022;6(13):4006-4014.
  5. Wood B, et al. Blood. 2018;131(12):1350-1359.
  6. Pulsipher M, et al. Blood. 2015;125(22):3501-3508.
  1. Pulsipher M, et al. Blood Cancer Discov. 2022;3(1):66-81.
  2. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Acute Lymphoblastic Leukemia V.2.2021. © National Comprehensive Cancer Network, Inc. 2020. 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.