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Drug induced interstitial lung disease in oncology phase I trials
Interstitial lung disease is a serious drug‐related condition that can cause life threatening organ failure. The incidence and risk factors of drug‐induced interstitial lung disease (DILD) are unknown in oncology phase I trials. This study analyzed clinical information from 8906 patients with malign...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198943/ https://www.ncbi.nlm.nih.gov/pubmed/27685762 http://dx.doi.org/10.1111/cas.13087 |
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author | Yonemori, Kan Hirakawa, Akihiro Kawachi, Asuka Kinoshita, Fumie Okuma, Hitomi Nishikawa, Tadaaki Tamura, Kenji Fujiwara, Yasuhiro Takebe, Naoko |
author_facet | Yonemori, Kan Hirakawa, Akihiro Kawachi, Asuka Kinoshita, Fumie Okuma, Hitomi Nishikawa, Tadaaki Tamura, Kenji Fujiwara, Yasuhiro Takebe, Naoko |
author_sort | Yonemori, Kan |
collection | PubMed |
description | Interstitial lung disease is a serious drug‐related condition that can cause life threatening organ failure. The incidence and risk factors of drug‐induced interstitial lung disease (DILD) are unknown in oncology phase I trials. This study analyzed clinical information from 8906 patients with malignancies who were enrolled in 470 phase I trials sponsored by the Cancer Therapy Evaluation Program, National Cancer Institute, from 1988 to 2014. Logistic and Cox statistical analyses were utilized to determine clinical differences between patients who developed DILD and patients who did not. In this study, the overall incidence rate of patients with pulmonary toxicity was 2.7%. The overall incidence rate for DILD was 0.77%, whereas for grade 3 or 4 DILD it was 0.31%. Median time to occurrence of DILD was 1.4 months. The Cox hazard analysis indicated smaller body surface area and a combination of thoracic radiation with investigational drug regimens were significant risk factors for time to occurrence of interstitial lung disease. Investigators should carefully monitor for DILD in oncology patients enrolled in phase I trials with identified risk factors. A 6‐month observation period would be sufficient to detect the onset of most DILD in such patients. |
format | Online Article Text |
id | pubmed-5198943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51989432016-12-30 Drug induced interstitial lung disease in oncology phase I trials Yonemori, Kan Hirakawa, Akihiro Kawachi, Asuka Kinoshita, Fumie Okuma, Hitomi Nishikawa, Tadaaki Tamura, Kenji Fujiwara, Yasuhiro Takebe, Naoko Cancer Sci Original Articles Interstitial lung disease is a serious drug‐related condition that can cause life threatening organ failure. The incidence and risk factors of drug‐induced interstitial lung disease (DILD) are unknown in oncology phase I trials. This study analyzed clinical information from 8906 patients with malignancies who were enrolled in 470 phase I trials sponsored by the Cancer Therapy Evaluation Program, National Cancer Institute, from 1988 to 2014. Logistic and Cox statistical analyses were utilized to determine clinical differences between patients who developed DILD and patients who did not. In this study, the overall incidence rate of patients with pulmonary toxicity was 2.7%. The overall incidence rate for DILD was 0.77%, whereas for grade 3 or 4 DILD it was 0.31%. Median time to occurrence of DILD was 1.4 months. The Cox hazard analysis indicated smaller body surface area and a combination of thoracic radiation with investigational drug regimens were significant risk factors for time to occurrence of interstitial lung disease. Investigators should carefully monitor for DILD in oncology patients enrolled in phase I trials with identified risk factors. A 6‐month observation period would be sufficient to detect the onset of most DILD in such patients. John Wiley and Sons Inc. 2016-12-29 2016-12 /pmc/articles/PMC5198943/ /pubmed/27685762 http://dx.doi.org/10.1111/cas.13087 Text en © 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Yonemori, Kan Hirakawa, Akihiro Kawachi, Asuka Kinoshita, Fumie Okuma, Hitomi Nishikawa, Tadaaki Tamura, Kenji Fujiwara, Yasuhiro Takebe, Naoko Drug induced interstitial lung disease in oncology phase I trials |
title | Drug induced interstitial lung disease in oncology phase I trials |
title_full | Drug induced interstitial lung disease in oncology phase I trials |
title_fullStr | Drug induced interstitial lung disease in oncology phase I trials |
title_full_unstemmed | Drug induced interstitial lung disease in oncology phase I trials |
title_short | Drug induced interstitial lung disease in oncology phase I trials |
title_sort | drug induced interstitial lung disease in oncology phase i trials |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198943/ https://www.ncbi.nlm.nih.gov/pubmed/27685762 http://dx.doi.org/10.1111/cas.13087 |
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