Blood cancer care is
always advancing.
Aim higher with
clonoSEQ®.
All 32 NCCN® Member Institutions use clonoSEQ to track MRD at a sensitivity of 10-6.1,2* Use clonoSEQ in routine clinical practice to help predict patient outcomes and support treatment decisions in lymphoid malignancies.3-9
JOIN THE MOVEMENT AND DETECT DEEPER
*Given adequate sample material.
Real-world experience and
peer-reviewed data
Helps monitor disease and inform decisions at each treatment stage
Multiple myeloma
Supports consistent monitoring during and after fixed-duration therapy
CLL
Predicts outcomes in pre- and post-transplant settings
Pediatric ALL
Allows monitoring of peripheral blood† as an alternative to frequent bone marrow assessments
adult ALL
†Blood-based testing in ALL is available as a CLIA-validated LDT and has not been cleared or approved by the FDA.
Is MRD testing part of your standard practice?
Why many clinicians make clonoSEQ standard in their practice.
clonoSEQ leverages the power of next-generation sequencing (NGS) to help clinicians monitor MRD throughout the course of multiple myeloma, CLL, and B-ALL care.1
Widely trusted
clonoSEQ is a mainstay of leading clinicians, including at all 32 NCCN® centers and hundreds of academic institutions and community clinics2
Broadly utilized
MRD assessment can be used throughout care, including during induction, maintenance, transplant, consolidation, and after treatment10-13
Highly sensitive
clonoSEQ technology can measure MRD at a sensitivity of 10-6 with adequate sample material1
Extensively accessible
Reimbursed by CMS and national plans covering >240 million lives (myeloma, ALL) and >150 million lives (CLL). Support for OOP costs is available for qualifying patients through Adaptive Assist™2
Discover specimen requirements, report tutorials, reimbursement support services for patients, and more
News and updates
Adaptive Biotechnologies Included in Key Abstracts at ASCO 2022 Supporting the Role of the clonoSEQ® Assay as a Standard for MRD Assessment Technology
Data demonstrate growing utilization of MRD to identify deep responses associated with the best patient outcomes
December, 2021
Adaptive Biotechnologies Announces New Data Demonstrating the Benefit of Serial MRD Testing with the clonoSEQ® Assay in Patients with Blood Cancers at the 63rd ASH Annual Meeting
What We’re Sharing Follow Us
This #bloodcancerawareness month, we are honoring Karen, a clonoSEQ patient with multiple myeloma, by sharing her story. clonoSEQ is FDA-cleared to assess MRD in patients with CLL, MM, or B-ALL. For important info, incl. sample types & test limitations: https://t.co/sE39cuZxFD pic.twitter.com/ZmTYQGopLx
— clonoSEQ (@clonoSEQ) September 6, 2022
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 minimal 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). CLL Clonality (ID) Tests will also produce an IGHV status result, which is provided as a CLIA-validated laboratory developed test (LDT) but which has not been cleared or approved by the FDA. Additionally, clonoSEQ is available for use in other lymphoid cancers and specimen types as a CLIA-validated LDT. For important information about the FDA-cleared uses of clonoSEQ including test limitations, please visit clonoSEQ.com/technical-summary.
References
- clonoSEQ®. [technical summary]. Seattle, WA. Adaptive Biotechnologies; 2020. https://www.clonoseq.com/technical-summary/
- Data on file. Adaptive Biotechnologies. 2021.
- Munshi N, et al. Blood Adv. 2020;4(23):5988-5999.
- Berry D, et al. JAMA Oncol. 2017;3(7):e170580.
- Molica S, et al. Clin Lymphoma Myeloma Leuk. 2019;19(7):423-430.
- San-Miguel J, et al. Blood. 2021. doi: 10.1182/blood.2020010439
- Martinez-Lopez J, et al. J Hematol Oncol. 2021;14(1):126.
- Friend B, et al. Pediatr Blood Cancer. 2020. doi: 10.1002/pbc.28079
- Al-Sawaf O, et al. J Clin Oncol. 2021. doi: 10.1200/JCO.21.01181
- 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 November 1, 2021. 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.
- Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma V.4.2021. © National Comprehensive Cancer Network, Inc. 2021. All rights reserved. Accessed October 26, 2021. 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.
- Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Pediatric Acute Lymphoblastic Leukemia V.1.2022. © National Comprehensive Cancer Network, Inc. 2021. All rights reserved. Accessed November 4, 2021. 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.
- 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. 2021. All rights reserved. Accessed October 26, 2021. 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.