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Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma

Central nervous sytem recurrence of diffuse large B-cell lymphoma is an uncommon but devastating event, making identification of patients at high risk for relapse within the central nervous system essential for clinicians. Modern risk stratification includes both clinical and biological features. A...

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Autores principales: Qualls, David, Abramson, Jeremy S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312016/
https://www.ncbi.nlm.nih.gov/pubmed/30573511
http://dx.doi.org/10.3324/haematol.2018.195834
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author Qualls, David
Abramson, Jeremy S.
author_facet Qualls, David
Abramson, Jeremy S.
author_sort Qualls, David
collection PubMed
description Central nervous sytem recurrence of diffuse large B-cell lymphoma is an uncommon but devastating event, making identification of patients at high risk for relapse within the central nervous system essential for clinicians. Modern risk stratification includes both clinical and biological features. A validated clinical risk model employing the five traditional International Prognostic Index risk factors plus renal or adrenal involvement can identify a high-risk patient population with a central nervous system recurrence risk of greater than 10%. Lymphoma involvement of certain discrete extranodal sites such as the testis also confers increased risk, even in stage I disease. Adverse biological risk factors for central nervous system relapse include presence of translocations of MYC, BCL2 and/or BCL6, in so-called double- or triple-hit lymphoma. Immunohistochemically detectable co-expression of MYC and BCL2 in the absence of translocations also portends an increased risk of relapse within the central nervous system, particularly in the setting of the activated B-cell-like subtype of diffuse large B-cell lymphoma. The role, method, and timing of prophylactic therapy remain controversial based on the available data. We review both intrathecal and systemic strategies for prophylaxis in high-risk patients. Our preference is for systemic methotrexate in concert with standard chemoimmunotherapy in the majority of cases. Several novel agents have also demonstrated clinical activity in primary and secondary central nervous system lymphoma and warrant future investigation in the prophylactic setting.
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spelling pubmed-63120162019-01-04 Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma Qualls, David Abramson, Jeremy S. Haematologica Review Article Central nervous sytem recurrence of diffuse large B-cell lymphoma is an uncommon but devastating event, making identification of patients at high risk for relapse within the central nervous system essential for clinicians. Modern risk stratification includes both clinical and biological features. A validated clinical risk model employing the five traditional International Prognostic Index risk factors plus renal or adrenal involvement can identify a high-risk patient population with a central nervous system recurrence risk of greater than 10%. Lymphoma involvement of certain discrete extranodal sites such as the testis also confers increased risk, even in stage I disease. Adverse biological risk factors for central nervous system relapse include presence of translocations of MYC, BCL2 and/or BCL6, in so-called double- or triple-hit lymphoma. Immunohistochemically detectable co-expression of MYC and BCL2 in the absence of translocations also portends an increased risk of relapse within the central nervous system, particularly in the setting of the activated B-cell-like subtype of diffuse large B-cell lymphoma. The role, method, and timing of prophylactic therapy remain controversial based on the available data. We review both intrathecal and systemic strategies for prophylaxis in high-risk patients. Our preference is for systemic methotrexate in concert with standard chemoimmunotherapy in the majority of cases. Several novel agents have also demonstrated clinical activity in primary and secondary central nervous system lymphoma and warrant future investigation in the prophylactic setting. Ferrata Storti Foundation 2019-01 /pmc/articles/PMC6312016/ /pubmed/30573511 http://dx.doi.org/10.3324/haematol.2018.195834 Text en Copyright© 2019 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Review Article
Qualls, David
Abramson, Jeremy S.
Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma
title Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma
title_full Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma
title_fullStr Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma
title_full_unstemmed Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma
title_short Advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large B-cell lymphoma
title_sort advances in risk assessment and prophylaxis for central nervous system relapse in diffuse large b-cell lymphoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312016/
https://www.ncbi.nlm.nih.gov/pubmed/30573511
http://dx.doi.org/10.3324/haematol.2018.195834
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