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A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811)
Safety and efficacy of intrapericardial (ipc) instillation of bleomycin (BLM) following pericardial drainage in patients with malignant pericardial effusion (MPE) remain unclear. Patients with pathologically documented lung cancer, who had undergone pericardial drainage for MPE within 72 h of enrolm...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2658533/ https://www.ncbi.nlm.nih.gov/pubmed/19156149 http://dx.doi.org/10.1038/sj.bjc.6604866 |
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author | Kunitoh, H Tamura, T Shibata, T Imai, M Nishiwaki, Y Nishio, M Yokoyama, A Watanabe, K Noda, K Saijo, N |
author_facet | Kunitoh, H Tamura, T Shibata, T Imai, M Nishiwaki, Y Nishio, M Yokoyama, A Watanabe, K Noda, K Saijo, N |
author_sort | Kunitoh, H |
collection | PubMed |
description | Safety and efficacy of intrapericardial (ipc) instillation of bleomycin (BLM) following pericardial drainage in patients with malignant pericardial effusion (MPE) remain unclear. Patients with pathologically documented lung cancer, who had undergone pericardial drainage for MPE within 72 h of enrolment, were randomised to either arm A (observation alone after drainage) or arm B (ipc BLM at 15 mg, followed by additional ipc BLM 10 mg every 48 h). The drainage tube was removed when daily drainage was 20 ml or less. The primary end point was survival with MPE control (effusion failure-free survival, EFFS) at 2 months. Eighty patients were enrolled, and 79 were eligible. Effusion failure-free survival at 2 months was 29% in arm A and 46% in arm B (one-sided P=0.086 by Fisher’s exact test). Arm B tended to favour EFFS, with a hazard ratio of 0.64 (95% confidence interval: 0.40–1.03, one-sided P=0.030 by log-rank test). No significant differences in the acute toxicities or complications were observed. The median survival was 79 days and 119 days in arm A and arm B, respectively. This medium-sized trial failed to show statistical significance in the primary end point. Although ipc BLM appeared safe and effective in the management of MPE, the therapeutic advantage seems modest. |
format | Text |
id | pubmed-2658533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-26585332010-02-10 A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811) Kunitoh, H Tamura, T Shibata, T Imai, M Nishiwaki, Y Nishio, M Yokoyama, A Watanabe, K Noda, K Saijo, N Br J Cancer Clinical Study Safety and efficacy of intrapericardial (ipc) instillation of bleomycin (BLM) following pericardial drainage in patients with malignant pericardial effusion (MPE) remain unclear. Patients with pathologically documented lung cancer, who had undergone pericardial drainage for MPE within 72 h of enrolment, were randomised to either arm A (observation alone after drainage) or arm B (ipc BLM at 15 mg, followed by additional ipc BLM 10 mg every 48 h). The drainage tube was removed when daily drainage was 20 ml or less. The primary end point was survival with MPE control (effusion failure-free survival, EFFS) at 2 months. Eighty patients were enrolled, and 79 were eligible. Effusion failure-free survival at 2 months was 29% in arm A and 46% in arm B (one-sided P=0.086 by Fisher’s exact test). Arm B tended to favour EFFS, with a hazard ratio of 0.64 (95% confidence interval: 0.40–1.03, one-sided P=0.030 by log-rank test). No significant differences in the acute toxicities or complications were observed. The median survival was 79 days and 119 days in arm A and arm B, respectively. This medium-sized trial failed to show statistical significance in the primary end point. Although ipc BLM appeared safe and effective in the management of MPE, the therapeutic advantage seems modest. Nature Publishing Group 2009-02-10 2009-01-20 /pmc/articles/PMC2658533/ /pubmed/19156149 http://dx.doi.org/10.1038/sj.bjc.6604866 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Kunitoh, H Tamura, T Shibata, T Imai, M Nishiwaki, Y Nishio, M Yokoyama, A Watanabe, K Noda, K Saijo, N A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811) |
title | A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811) |
title_full | A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811) |
title_fullStr | A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811) |
title_full_unstemmed | A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811) |
title_short | A randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (JCOG9811) |
title_sort | randomised trial of intrapericardial bleomycin for malignant pericardial effusion with lung cancer (jcog9811) |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2658533/ https://www.ncbi.nlm.nih.gov/pubmed/19156149 http://dx.doi.org/10.1038/sj.bjc.6604866 |
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