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Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer
Cancer chemotherapy for haemodialysis patients has never been established. To elucidate the feasibility of cisplatin-based combination chemotherapy for haemodialysis patients with lung cancer, a dose escalation study was conducted. Five haemodialysis patients with lung cancer were treated with cispl...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376779/ https://www.ncbi.nlm.nih.gov/pubmed/12556954 http://dx.doi.org/10.1038/sj.bjc.6600687 |
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author | Watanabe, R Takiguchi, Y Moriya, T Oda, S Kurosu, K Tanabe, N Tatsumi, K Nagao, K Kuriyama, T |
author_facet | Watanabe, R Takiguchi, Y Moriya, T Oda, S Kurosu, K Tanabe, N Tatsumi, K Nagao, K Kuriyama, T |
author_sort | Watanabe, R |
collection | PubMed |
description | Cancer chemotherapy for haemodialysis patients has never been established. To elucidate the feasibility of cisplatin-based combination chemotherapy for haemodialysis patients with lung cancer, a dose escalation study was conducted. Five haemodialysis patients with lung cancer were treated with cisplatin and etoposide. A starting dose of 40 mg m(−2) of cisplatin on day 1 and 50 mg m(−2) of etoposide on days 1, 3 and 5 were administered as the first course for the first patient. Membrane haemodialysis was regularly performed three times a week and soon after the completion of therapy. By monitoring toxicity and pharmacokinetics data, the dose was escalated course by course and patient by patient. Dose escalation was completed for the first two patients resulting in full-dose chemotherapy consisting of 80 mg m(−2) of cisplatin on day 1 and 100 mg m(−2) of etoposide on days 1, 3 and 5. Multiple courses of the full-dose chemotherapy were administered to the other three patients. Toxicity was manageable and tolerable for all. Pharmacokinetics data were comparable to those from patients with normal renal function, except for potential long-lasting higher levels of free platinum in the renal insufficiency group. In conclusion, this standard-dose combination chemotherapy was feasible even for haemodialysis patients. |
format | Text |
id | pubmed-2376779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23767792009-09-10 Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer Watanabe, R Takiguchi, Y Moriya, T Oda, S Kurosu, K Tanabe, N Tatsumi, K Nagao, K Kuriyama, T Br J Cancer Clinical Cancer chemotherapy for haemodialysis patients has never been established. To elucidate the feasibility of cisplatin-based combination chemotherapy for haemodialysis patients with lung cancer, a dose escalation study was conducted. Five haemodialysis patients with lung cancer were treated with cisplatin and etoposide. A starting dose of 40 mg m(−2) of cisplatin on day 1 and 50 mg m(−2) of etoposide on days 1, 3 and 5 were administered as the first course for the first patient. Membrane haemodialysis was regularly performed three times a week and soon after the completion of therapy. By monitoring toxicity and pharmacokinetics data, the dose was escalated course by course and patient by patient. Dose escalation was completed for the first two patients resulting in full-dose chemotherapy consisting of 80 mg m(−2) of cisplatin on day 1 and 100 mg m(−2) of etoposide on days 1, 3 and 5. Multiple courses of the full-dose chemotherapy were administered to the other three patients. Toxicity was manageable and tolerable for all. Pharmacokinetics data were comparable to those from patients with normal renal function, except for potential long-lasting higher levels of free platinum in the renal insufficiency group. In conclusion, this standard-dose combination chemotherapy was feasible even for haemodialysis patients. Nature Publishing Group 2003-01-13 2003-01-28 /pmc/articles/PMC2376779/ /pubmed/12556954 http://dx.doi.org/10.1038/sj.bjc.6600687 Text en Copyright © 2003 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 Watanabe, R Takiguchi, Y Moriya, T Oda, S Kurosu, K Tanabe, N Tatsumi, K Nagao, K Kuriyama, T Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer |
title | Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer |
title_full | Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer |
title_fullStr | Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer |
title_full_unstemmed | Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer |
title_short | Feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer |
title_sort | feasibility of combination chemotherapy with cisplatin and etoposide for haemodialysis patients with lung cancer |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376779/ https://www.ncbi.nlm.nih.gov/pubmed/12556954 http://dx.doi.org/10.1038/sj.bjc.6600687 |
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