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Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma

In the era of personalized medicine, small-molecule inhibitors have become key to targeting many malignancies. Multiple hematologic malignancies are driven by small-molecule pathways that are seemingly ripe for such targeting. In this case report, we present a patient who was treated with a mitogen-...

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Detalles Bibliográficos
Autores principales: Young, Sarah, Kuzu, Amirah, Magill, Mike, Hajdenberg, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050040/
https://www.ncbi.nlm.nih.gov/pubmed/35494913
http://dx.doi.org/10.7759/cureus.23627
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author Young, Sarah
Kuzu, Amirah
Magill, Mike
Hajdenberg, Julio
author_facet Young, Sarah
Kuzu, Amirah
Magill, Mike
Hajdenberg, Julio
author_sort Young, Sarah
collection PubMed
description In the era of personalized medicine, small-molecule inhibitors have become key to targeting many malignancies. Multiple hematologic malignancies are driven by small-molecule pathways that are seemingly ripe for such targeting. In this case report, we present a patient who was treated with a mitogen-activated extracellular signal-regulated kinase (MEK) inhibitor for what was originally diagnosed as a histiocytic sarcoma. Re-biopsy ultimately revealed an anaplastic lymphoma kinase (ALK)-negative anaplastic large cell lymphoma (ALCL), but his disease initially showed a remarkable response to MEK inhibition. This case illustrates both the importance of obtaining high-quality biopsy specimens for diagnostic and molecular analysis as well as the need for further research into the molecular drivers of T-cell lymphomas that may be amenable to targeted therapies.
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spelling pubmed-90500402022-04-29 Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma Young, Sarah Kuzu, Amirah Magill, Mike Hajdenberg, Julio Cureus Pathology In the era of personalized medicine, small-molecule inhibitors have become key to targeting many malignancies. Multiple hematologic malignancies are driven by small-molecule pathways that are seemingly ripe for such targeting. In this case report, we present a patient who was treated with a mitogen-activated extracellular signal-regulated kinase (MEK) inhibitor for what was originally diagnosed as a histiocytic sarcoma. Re-biopsy ultimately revealed an anaplastic lymphoma kinase (ALK)-negative anaplastic large cell lymphoma (ALCL), but his disease initially showed a remarkable response to MEK inhibition. This case illustrates both the importance of obtaining high-quality biopsy specimens for diagnostic and molecular analysis as well as the need for further research into the molecular drivers of T-cell lymphomas that may be amenable to targeted therapies. Cureus 2022-03-29 /pmc/articles/PMC9050040/ /pubmed/35494913 http://dx.doi.org/10.7759/cureus.23627 Text en Copyright © 2022, Young et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pathology
Young, Sarah
Kuzu, Amirah
Magill, Mike
Hajdenberg, Julio
Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma
title Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma
title_full Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma
title_fullStr Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma
title_full_unstemmed Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma
title_short Partial Response to Small Molecule Inhibition in a Case of Anaplastic Large Cell Lymphoma
title_sort partial response to small molecule inhibition in a case of anaplastic large cell lymphoma
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050040/
https://www.ncbi.nlm.nih.gov/pubmed/35494913
http://dx.doi.org/10.7759/cureus.23627
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