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Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations
Mounting evidence underscores the clinical value of cytogenetic analysis in chronic lymphocytic leukemia (CLL), particularly as it allows the identification of complex karyotype, that has recently emerged as a prognostic and potentially predictive biomarker. That said, explicit recommendations regar...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984316/ https://www.ncbi.nlm.nih.gov/pubmed/35392482 http://dx.doi.org/10.1097/HS9.0000000000000707 |
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author | Baliakas, Panagiotis Espinet, Blanca Mellink, Clemens Jarosova, Marie Athanasiadou, Anastasia Ghia, Paolo Kater, Arnon P. Oscier, David Haferlach, Claudia Stamatopoulos, Kostas |
author_facet | Baliakas, Panagiotis Espinet, Blanca Mellink, Clemens Jarosova, Marie Athanasiadou, Anastasia Ghia, Paolo Kater, Arnon P. Oscier, David Haferlach, Claudia Stamatopoulos, Kostas |
author_sort | Baliakas, Panagiotis |
collection | PubMed |
description | Mounting evidence underscores the clinical value of cytogenetic analysis in chronic lymphocytic leukemia (CLL), particularly as it allows the identification of complex karyotype, that has recently emerged as a prognostic and potentially predictive biomarker. That said, explicit recommendations regarding the methodology and clinical interpretation of either chromosome banding analysis (CBA) or chromosome microarray analysis (CMA) are still lacking. We herein present the consensus of the Cytogenetic Steering Scientific Committee of ERIC, the European Research Initiative on CLL, regarding methodological issues as well as clinical interpretation of CBA/CMA and discuss their relevance in CLL. ERIC considers CBA standardized and feasible for CLL on the condition that standards are met, extending from the use of novel mitogens to the accurate interpretation of the findings. On the other hand, CMA, is also standardized, however, robust data on its clinical utility are still scarce. In conclusion, cytogenetic analysis is not yet mature enough to guide treatment choices in CLL. That notwithstanding, ERIC encourages the wide application of CBA, and potentially also CMA, in clinical trials in order to obtain robust evidence regarding the predictive value of specific cytogenetic profiles towards refining risk stratification and improving the management of patients with CLL. |
format | Online Article Text |
id | pubmed-8984316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-89843162022-04-06 Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations Baliakas, Panagiotis Espinet, Blanca Mellink, Clemens Jarosova, Marie Athanasiadou, Anastasia Ghia, Paolo Kater, Arnon P. Oscier, David Haferlach, Claudia Stamatopoulos, Kostas Hemasphere Guideline Article - Expert opinion Mounting evidence underscores the clinical value of cytogenetic analysis in chronic lymphocytic leukemia (CLL), particularly as it allows the identification of complex karyotype, that has recently emerged as a prognostic and potentially predictive biomarker. That said, explicit recommendations regarding the methodology and clinical interpretation of either chromosome banding analysis (CBA) or chromosome microarray analysis (CMA) are still lacking. We herein present the consensus of the Cytogenetic Steering Scientific Committee of ERIC, the European Research Initiative on CLL, regarding methodological issues as well as clinical interpretation of CBA/CMA and discuss their relevance in CLL. ERIC considers CBA standardized and feasible for CLL on the condition that standards are met, extending from the use of novel mitogens to the accurate interpretation of the findings. On the other hand, CMA, is also standardized, however, robust data on its clinical utility are still scarce. In conclusion, cytogenetic analysis is not yet mature enough to guide treatment choices in CLL. That notwithstanding, ERIC encourages the wide application of CBA, and potentially also CMA, in clinical trials in order to obtain robust evidence regarding the predictive value of specific cytogenetic profiles towards refining risk stratification and improving the management of patients with CLL. Lippincott Williams & Wilkins 2022-03-25 /pmc/articles/PMC8984316/ /pubmed/35392482 http://dx.doi.org/10.1097/HS9.0000000000000707 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Hematology Association. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Guideline Article - Expert opinion Baliakas, Panagiotis Espinet, Blanca Mellink, Clemens Jarosova, Marie Athanasiadou, Anastasia Ghia, Paolo Kater, Arnon P. Oscier, David Haferlach, Claudia Stamatopoulos, Kostas Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations |
title | Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations |
title_full | Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations |
title_fullStr | Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations |
title_full_unstemmed | Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations |
title_short | Cytogenetics in Chronic Lymphocytic Leukemia: ERIC Perspectives and Recommendations |
title_sort | cytogenetics in chronic lymphocytic leukemia: eric perspectives and recommendations |
topic | Guideline Article - Expert opinion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984316/ https://www.ncbi.nlm.nih.gov/pubmed/35392482 http://dx.doi.org/10.1097/HS9.0000000000000707 |
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