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Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib
We describe the case of a 71-year-old Caucasian female with primary disseminated non-small cell cancer of the lung, presented for palliative radiotherapy of metastatic spread to the 9th and 11th thoracic vertebrae without intramedullary growth. Palliative radiotherapy with daily fractions of 3 Gy an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313465/ https://www.ncbi.nlm.nih.gov/pubmed/25631068 http://dx.doi.org/10.1186/s13014-015-0334-7 |
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author | Lewitzki, Victor Andratschke, Nicolaus Kuhnt, Thomas Hildebrandt, Guido |
author_facet | Lewitzki, Victor Andratschke, Nicolaus Kuhnt, Thomas Hildebrandt, Guido |
author_sort | Lewitzki, Victor |
collection | PubMed |
description | We describe the case of a 71-year-old Caucasian female with primary disseminated non-small cell cancer of the lung, presented for palliative radiotherapy of metastatic spread to the 9th and 11th thoracic vertebrae without intramedullary growth. Palliative radiotherapy with daily fractions of 3 Gy and a cumulative dose of 36 Gy to thoracic vertebrae 8-12 was performed. The patient received concomitantly 250 mg gefitinib daily. After a latent period of 16 months, the patient developed symptoms of myelitis. Magnetic resonance imaging (MRI) did not reveal any bony or intraspinal tumor progression, but spinal cord signal alteration. No response to steroids was achieved. The neurological symptoms were progressive in August 2013 with the right leg being completely plegic. The left leg was incompletely paralyzed. Deep and superficial sensitivity was also diminished bilaterally. The patient was completely urinary and anally incontinent. Contrary to the clinical findings, a follow-up MRI (July 2013) showed amelioration of the former signal alterations in the spinal cord. The diagnosis of paraneoplastic myelopathy was refuted by a negative test for autologous antibodies. At the last clinical visit in May 2014, the neurological symptoms were stable. The last tumor-specific treatment the patient is receiving is erlotinib 125 mg/d. We reviewed the literature and found no reported cases of radiation myelopathy after the treatment in such a setting. The calculated probability of such complication after radiotherapy alone is statistically measurable at the level of 0.02%. We suppose that gefitinib could also play a role in the development of this rare complication. |
format | Online Article Text |
id | pubmed-4313465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43134652015-02-03 Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib Lewitzki, Victor Andratschke, Nicolaus Kuhnt, Thomas Hildebrandt, Guido Radiat Oncol Case Report We describe the case of a 71-year-old Caucasian female with primary disseminated non-small cell cancer of the lung, presented for palliative radiotherapy of metastatic spread to the 9th and 11th thoracic vertebrae without intramedullary growth. Palliative radiotherapy with daily fractions of 3 Gy and a cumulative dose of 36 Gy to thoracic vertebrae 8-12 was performed. The patient received concomitantly 250 mg gefitinib daily. After a latent period of 16 months, the patient developed symptoms of myelitis. Magnetic resonance imaging (MRI) did not reveal any bony or intraspinal tumor progression, but spinal cord signal alteration. No response to steroids was achieved. The neurological symptoms were progressive in August 2013 with the right leg being completely plegic. The left leg was incompletely paralyzed. Deep and superficial sensitivity was also diminished bilaterally. The patient was completely urinary and anally incontinent. Contrary to the clinical findings, a follow-up MRI (July 2013) showed amelioration of the former signal alterations in the spinal cord. The diagnosis of paraneoplastic myelopathy was refuted by a negative test for autologous antibodies. At the last clinical visit in May 2014, the neurological symptoms were stable. The last tumor-specific treatment the patient is receiving is erlotinib 125 mg/d. We reviewed the literature and found no reported cases of radiation myelopathy after the treatment in such a setting. The calculated probability of such complication after radiotherapy alone is statistically measurable at the level of 0.02%. We suppose that gefitinib could also play a role in the development of this rare complication. BioMed Central 2015-01-29 /pmc/articles/PMC4313465/ /pubmed/25631068 http://dx.doi.org/10.1186/s13014-015-0334-7 Text en © Lewitzki et al. ; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Lewitzki, Victor Andratschke, Nicolaus Kuhnt, Thomas Hildebrandt, Guido Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib |
title | Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib |
title_full | Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib |
title_fullStr | Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib |
title_full_unstemmed | Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib |
title_short | Radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib |
title_sort | radiation myelitis after hypofractionated radiotherapy with concomitant gefitinib |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313465/ https://www.ncbi.nlm.nih.gov/pubmed/25631068 http://dx.doi.org/10.1186/s13014-015-0334-7 |
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