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From biomarkers to models in the changing landscape of chronic lymphocytic leukemia: Evolve or become extinct

Authors :
Instituto de Salud Carlos III
European Commission
Junta de Castilla y León
Fundación Memoria de D. Samuel Solorzano Barruso
Red Temática de Investigación Cooperativa en Cáncer (España)
Centro de Investigación Biomédica en Red Cáncer (España)
Fundacion de la Sociedad Española de Hematología y Hemoterapia
Asociación Española Contra el Cáncer
Janssen Research and Development
González-Gascón y Marín, Isabel
Muñoz-Novas, Carolina
Rodríguez-Vicente, Ana Eugenia
Quijada-Álamo, Miguel
Hernández-Sánchez, María
Pérez-Carretero, Claudia
Ramos-Ascanio, Victoria
Hernández-Rivas, José Ángel
Instituto de Salud Carlos III
European Commission
Junta de Castilla y León
Fundación Memoria de D. Samuel Solorzano Barruso
Red Temática de Investigación Cooperativa en Cáncer (España)
Centro de Investigación Biomédica en Red Cáncer (España)
Fundacion de la Sociedad Española de Hematología y Hemoterapia
Asociación Española Contra el Cáncer
Janssen Research and Development
González-Gascón y Marín, Isabel
Muñoz-Novas, Carolina
Rodríguez-Vicente, Ana Eugenia
Quijada-Álamo, Miguel
Hernández-Sánchez, María
Pérez-Carretero, Claudia
Ramos-Ascanio, Victoria
Hernández-Rivas, José Ángel
Publication Year :
2021

Abstract

Chronic lymphocytic leukemia (CLL) is an extremely heterogeneous disease. With the advent of oral targeted agents (Tas) the treatment of CLL has undergone a revolution, which has been accompanied by an improvement in patient’s survival and quality of life. This paradigm shift also affects the value of prognostic and predictive biomarkers and prognostic models, most of them inherited from the chemoimmunotherapy era but with a different behavior with Tas. This review discusses: (i) the role of the most relevant prognostic and predictive biomarkers in the setting of Tas; and (ii) the validity of classic and new scoring systems in the context of Tas. In addition, a critical point of view about predictive biomarkers with special emphasis on 11q deletion, novel resistance mutations, TP53 abnormalities, IGHV mutational status, complex karyotype and NOTCH1 mutations is stated. We also go over prognostic models in early stage CLL such as IPS-E. Finally, we provide an overview of the applicability of the CLL-IPI for patients treated with Tas, as well as the emergence of new models, generated with data from patients treated with Tas.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1306017371
Document Type :
Electronic Resource