Minimal residual disease (MRD) assessment is an important endpoint in the treatment of chronic lymphocytic leukaemia (CLL). It is highly predictive of prolonged progression-free survival (PFS) and overall survival and could be considered a surrogate for PFS in the context of chemoimmunotherapy based treatment. Evaluation of MRD level by flow cytometry or molecular techniques in the era of the new BCR and Bcl-2 targeted inhibitors could identify the most cost-effective and durable treatment sequencing. A therapeutic approach guided by the level of MRD might also determine which patients would benefit from an early stop or consolidation therapy. In this review, we discuss the different MRD methods of analysis, which source of tumour samples must be analysed, the future role of the detection of circulating tumour DNA, and the potential role of MRD negativity in clinical practice in the modern era of CLL therapy.
Keywords: Chronic lymphocytic leukemia; Citometría de flujo; Enfermedad mínima residual; Flow cytometry; Ibrutinib; Idelalisib; Leucemia linfocítica crónica; Minimal residual disease; Obinutuzumab; Venetoclax.
Copyright © 2017 Elsevier España, S.L.U. All rights reserved.