Utility of Measurable Residual Disease (MRD) Assessment in Mantle Cell Lymphoma
Details
Publication Year 2023-08,Volume 24,Issue #8,Page 929-947
Journal Title
Current Treatment Options in Oncology
Publication Type
Review
Abstract
Mantle cell lymphoma (MCL) treatment advances have significantly improved disease-free remission, with greater focus in clinical trials being placed on measurable residual disease (MRD) as a marker of subclinical disease assessment. While this concept is used extensively in other haematological neoplasms, there is yet to be a consensus on the threshold for MRD in MCL that demonstrates prognostic and therapeutic significance, and in this context has yet to reach routine clinical practice. The historical long-term method for MCL MRD assessment has been real-time quantitative polymerase chain reaction (PCR), targeting the clonal immunoglobulin heavy locus (IGH) rearrangement or the IGH::CCND1 translocation rearrangement. A significant problem at present relates to identifying alternative assays for patients who do not have a suitable molecular target by this method. This article reviews existing techniques used in MRD assessment for MCL and describes novel methods which may overcome existing limitations, including next-generation sequencing modalities. The use of circulating tumour DNA is explored, with techniques such as CAPP-Seq and PhasED-Seq demonstrating promise in B-lymphoproliferative disorders, though application in MCL requires further study. The other aspect of practice using MRD is identifying therapeutic options which can address a subclinical molecular relapse. Developing suitable interventions that can alter the disease trajectory based on longitudinal MRD kinetics are needed to justify its incorporation into standard care.
Publisher
Springer Nature
Keywords
Adult; Humans; *Lymphoma, Mantle-Cell/diagnosis/genetics/therapy; Neoplasm Recurrence, Local/genetics; Translocation, Genetic; Prognosis; Neoplasm, Residual/diagnosis/genetics; Circulating tumour DNA; Mantle cell lymphoma; Measurable residual disease; Minimal residual disease; Next-generation sequencing
Department(s)
Clinical Haematology; Pathology
PubMed ID
37249800
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