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Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome

Appropriate counseling of patients with autoimmune connective tissue disorders (ACTDs) is often challenging for radiation oncologists, especially regarding anticipated side-effects of radiation treatment. These patients can have highly variable and unpredictable sequelae from radiation therapy, and...

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Autores principales: Valle, Luca, Katz, James, Duffy, Austin, Hueman, Matthew, Wang, Hao-Wei, Hughes, Marybeth, Sissung, Tristan, Figg, William, Citrin, Deborah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Institute of Radiology. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461731/
https://www.ncbi.nlm.nih.gov/pubmed/36101738
http://dx.doi.org/10.1259/bjrcr.20210188
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author Valle, Luca
Katz, James
Duffy, Austin
Hueman, Matthew
Wang, Hao-Wei
Hughes, Marybeth
Sissung, Tristan
Figg, William
Citrin, Deborah
author_facet Valle, Luca
Katz, James
Duffy, Austin
Hueman, Matthew
Wang, Hao-Wei
Hughes, Marybeth
Sissung, Tristan
Figg, William
Citrin, Deborah
author_sort Valle, Luca
collection PubMed
description Appropriate counseling of patients with autoimmune connective tissue disorders (ACTDs) is often challenging for radiation oncologists, especially regarding anticipated side-effects of radiation treatment. These patients can have highly variable and unpredictable sequelae from radiation therapy, and the uncertainty builds when radiation is convoluted by the addition of concurrent chemotherapy. While many patients may experience a mild intensification of toxicity above what is expected, some patients experience much more severe toxicity. These patients become critical learning cases, enabling a better understanding of the delicate and complex ways in which radiation response is altered in the context of ACTDs while allowing other patients with similar ACTD profiles to benefit from past experience. Our report makes an important contribution to this space by describing a particularly severe case of toxicity that manifested in such a patient and the ensuing clinical decision-making. Comprehensive genotyping of classic pharmacokinetic and pharmacodynamic pathway genes (including mutations in DPD and CDA) did not reveal any signatures that might explain her enhanced toxicity and we demonstrate that severe toxicity can still manifest in the era of modern conformal radiation treatments for rectal cancer. We urge caution in the treatment of patients with rare ACTDs, but also emphasize that curative treatment should not be withheld in such patients. We conclude by advocating for the development and maintenance of a prospective multiinstitutional database of patients with ACTDs to help inform and improve future practice.
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spelling pubmed-94617312022-09-12 Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome Valle, Luca Katz, James Duffy, Austin Hueman, Matthew Wang, Hao-Wei Hughes, Marybeth Sissung, Tristan Figg, William Citrin, Deborah BJR Case Rep Case Report Appropriate counseling of patients with autoimmune connective tissue disorders (ACTDs) is often challenging for radiation oncologists, especially regarding anticipated side-effects of radiation treatment. These patients can have highly variable and unpredictable sequelae from radiation therapy, and the uncertainty builds when radiation is convoluted by the addition of concurrent chemotherapy. While many patients may experience a mild intensification of toxicity above what is expected, some patients experience much more severe toxicity. These patients become critical learning cases, enabling a better understanding of the delicate and complex ways in which radiation response is altered in the context of ACTDs while allowing other patients with similar ACTD profiles to benefit from past experience. Our report makes an important contribution to this space by describing a particularly severe case of toxicity that manifested in such a patient and the ensuing clinical decision-making. Comprehensive genotyping of classic pharmacokinetic and pharmacodynamic pathway genes (including mutations in DPD and CDA) did not reveal any signatures that might explain her enhanced toxicity and we demonstrate that severe toxicity can still manifest in the era of modern conformal radiation treatments for rectal cancer. We urge caution in the treatment of patients with rare ACTDs, but also emphasize that curative treatment should not be withheld in such patients. We conclude by advocating for the development and maintenance of a prospective multiinstitutional database of patients with ACTDs to help inform and improve future practice. The British Institute of Radiology. 2022-02-24 /pmc/articles/PMC9461731/ /pubmed/36101738 http://dx.doi.org/10.1259/bjrcr.20210188 Text en © 2022 The Authors. Published by the British Institute of Radiology https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Valle, Luca
Katz, James
Duffy, Austin
Hueman, Matthew
Wang, Hao-Wei
Hughes, Marybeth
Sissung, Tristan
Figg, William
Citrin, Deborah
Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome
title Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome
title_full Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome
title_fullStr Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome
title_full_unstemmed Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome
title_short Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome
title_sort enhanced toxicity to chemoradiation in a patient with anti-jo-1-antisynthetase syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9461731/
https://www.ncbi.nlm.nih.gov/pubmed/36101738
http://dx.doi.org/10.1259/bjrcr.20210188
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