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Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule
We investigated whether carboplatin pharmacokinetics is altered when the drug is delivered daily over 5 days, compared to a single‐day infusion. Carboplatin was infused in 11 patients with lung cancer, who were randomly assigned to 2 groups. In the first group, the agent was administered on a conven...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921454/ https://www.ncbi.nlm.nih.gov/pubmed/9247610 http://dx.doi.org/10.1111/j.1349-7006.1997.tb00412.x |
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author | Ando, Yuichi Minami, Hironobu Saka, Hideo Ando, Masahiko Sugiura, Seiji Sakai, Shuzo Shimokata, Kaoru |
author_facet | Ando, Yuichi Minami, Hironobu Saka, Hideo Ando, Masahiko Sugiura, Seiji Sakai, Shuzo Shimokata, Kaoru |
author_sort | Ando, Yuichi |
collection | PubMed |
description | We investigated whether carboplatin pharmacokinetics is altered when the drug is delivered daily over 5 days, compared to a single‐day infusion. Carboplatin was infused in 11 patients with lung cancer, who were randomly assigned to 2 groups. In the first group, the agent was administered on a conventional single‐day schedule in the first course and then on a 5‐day schedule in the second course. In the second group, the order was reversed (crossover design). The dose was calculated using Calvert's formula with 24 h creatinine clearance (Ccr, ml/min) as a substitute for glomerular filtration rate (GFR): carboplatin (mg) = AUC X (Ccr+25), where AUC denotes the area under the concentration versus time curve (mg ml(–1) min). No difference of carboplatin clearance between the single‐day and 5‐day schedule was observed (94.8± 19.9 versus 96.1+29.9 ml/min, P=0.818, paired t test). The formula systematically overestimated the carboplatin clearance; the ratio of estimated clearance/ observed clearance ranged from 1.01 to 1.58 (median 1.28; 95% confidence interval, 1.18 to 1.39). We concluded that the individual dosing strategy based on renal function can be applied with a 5‐day schedule as well as a single‐day schedule. Carboplatin is overdosed when Ccr is substituted for GFR in Calvert's formula. |
format | Online Article Text |
id | pubmed-5921454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59214542018-05-11 Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule Ando, Yuichi Minami, Hironobu Saka, Hideo Ando, Masahiko Sugiura, Seiji Sakai, Shuzo Shimokata, Kaoru Jpn J Cancer Res Article We investigated whether carboplatin pharmacokinetics is altered when the drug is delivered daily over 5 days, compared to a single‐day infusion. Carboplatin was infused in 11 patients with lung cancer, who were randomly assigned to 2 groups. In the first group, the agent was administered on a conventional single‐day schedule in the first course and then on a 5‐day schedule in the second course. In the second group, the order was reversed (crossover design). The dose was calculated using Calvert's formula with 24 h creatinine clearance (Ccr, ml/min) as a substitute for glomerular filtration rate (GFR): carboplatin (mg) = AUC X (Ccr+25), where AUC denotes the area under the concentration versus time curve (mg ml(–1) min). No difference of carboplatin clearance between the single‐day and 5‐day schedule was observed (94.8± 19.9 versus 96.1+29.9 ml/min, P=0.818, paired t test). The formula systematically overestimated the carboplatin clearance; the ratio of estimated clearance/ observed clearance ranged from 1.01 to 1.58 (median 1.28; 95% confidence interval, 1.18 to 1.39). We concluded that the individual dosing strategy based on renal function can be applied with a 5‐day schedule as well as a single‐day schedule. Carboplatin is overdosed when Ccr is substituted for GFR in Calvert's formula. Blackwell Publishing Ltd 1997-05 /pmc/articles/PMC5921454/ /pubmed/9247610 http://dx.doi.org/10.1111/j.1349-7006.1997.tb00412.x Text en |
spellingShingle | Article Ando, Yuichi Minami, Hironobu Saka, Hideo Ando, Masahiko Sugiura, Seiji Sakai, Shuzo Shimokata, Kaoru Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule |
title | Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule |
title_full | Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule |
title_fullStr | Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule |
title_full_unstemmed | Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule |
title_short | Pharmacokinetic Study of Carboplatin Given on a 5‐Day Intravenous Schedule |
title_sort | pharmacokinetic study of carboplatin given on a 5‐day intravenous schedule |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921454/ https://www.ncbi.nlm.nih.gov/pubmed/9247610 http://dx.doi.org/10.1111/j.1349-7006.1997.tb00412.x |
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