Cargando…

Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer

Irinotecan and cisplatin demonstrated promising outcomes in extensive-stage small-cell lung cancer. According to the dosage and schedule of irinotecan, efficacy and toxicity profiles showed subtle differences. This study was designed to evaluate efficacy and toxicity of 3-week schedule of irinotecan...

Descripción completa

Detalles Bibliográficos
Autores principales: Hong, Y S, Lee, H R, Park, S, Lee, S C, Hwang, I G, Park, B-B, Lee, J, Ahn, J S, Ahn, M-J, Lim, H Y, Park, K
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360764/
https://www.ncbi.nlm.nih.gov/pubmed/17133266
http://dx.doi.org/10.1038/sj.bjc.6603500
_version_ 1782153129971679232
author Hong, Y S
Lee, H R
Park, S
Lee, S C
Hwang, I G
Park, B-B
Lee, J
Ahn, J S
Ahn, M-J
Lim, H Y
Park, K
author_facet Hong, Y S
Lee, H R
Park, S
Lee, S C
Hwang, I G
Park, B-B
Lee, J
Ahn, J S
Ahn, M-J
Lim, H Y
Park, K
author_sort Hong, Y S
collection PubMed
description Irinotecan and cisplatin demonstrated promising outcomes in extensive-stage small-cell lung cancer. According to the dosage and schedule of irinotecan, efficacy and toxicity profiles showed subtle differences. This study was designed to evaluate efficacy and toxicity of 3-week schedule of irinotecan/cisplatin in patients with previously untreated extensive-stage small-cell lung cancer. The primary objective was to evaluate response rate and secondary objectives were overall survival and progression-free survival. Patients with previously untreated extensive-stage small-cell lung cancer were enrolled. Irinotecan 65 mg m(−2) was administered on days 1 and 8 and cisplatin 60 mg m(−2) on day 1. Treatment was repeated every 3 weeks. Seven out of 54 patients (13.0%) had complete response, and partial response was observed in 33 (61.1%). The overall response rate was 74.1% (95% CI; 62.0–82.2%). Stable disease was observed in eight (14.8%) and no progressive disease was observed. After a median follow-up duration of 28.7 months, the median overall survival and progressive-free survival were 13.6 and 6.5 months, respectively. Major grade 3/4 toxicities were neutropenia (50.0%), anorexia (42.6%), diarrhoea (29.6%), fatigue (29.6%) and vomiting (13.0%). There was one treatment-related death owing to pneumonia. Three-week schedule of irinotecan/cisplatin showed effective antitumour activity and moderate toxicities in patients with previously untreated extensive-stage small-cell lung cancer.
format Text
id pubmed-2360764
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-23607642009-09-10 Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer Hong, Y S Lee, H R Park, S Lee, S C Hwang, I G Park, B-B Lee, J Ahn, J S Ahn, M-J Lim, H Y Park, K Br J Cancer Clinical Study Irinotecan and cisplatin demonstrated promising outcomes in extensive-stage small-cell lung cancer. According to the dosage and schedule of irinotecan, efficacy and toxicity profiles showed subtle differences. This study was designed to evaluate efficacy and toxicity of 3-week schedule of irinotecan/cisplatin in patients with previously untreated extensive-stage small-cell lung cancer. The primary objective was to evaluate response rate and secondary objectives were overall survival and progression-free survival. Patients with previously untreated extensive-stage small-cell lung cancer were enrolled. Irinotecan 65 mg m(−2) was administered on days 1 and 8 and cisplatin 60 mg m(−2) on day 1. Treatment was repeated every 3 weeks. Seven out of 54 patients (13.0%) had complete response, and partial response was observed in 33 (61.1%). The overall response rate was 74.1% (95% CI; 62.0–82.2%). Stable disease was observed in eight (14.8%) and no progressive disease was observed. After a median follow-up duration of 28.7 months, the median overall survival and progressive-free survival were 13.6 and 6.5 months, respectively. Major grade 3/4 toxicities were neutropenia (50.0%), anorexia (42.6%), diarrhoea (29.6%), fatigue (29.6%) and vomiting (13.0%). There was one treatment-related death owing to pneumonia. Three-week schedule of irinotecan/cisplatin showed effective antitumour activity and moderate toxicities in patients with previously untreated extensive-stage small-cell lung cancer. Nature Publishing Group 2006-12-18 2006-11-28 /pmc/articles/PMC2360764/ /pubmed/17133266 http://dx.doi.org/10.1038/sj.bjc.6603500 Text en Copyright © 2006 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
Hong, Y S
Lee, H R
Park, S
Lee, S C
Hwang, I G
Park, B-B
Lee, J
Ahn, J S
Ahn, M-J
Lim, H Y
Park, K
Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer
title Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer
title_full Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer
title_fullStr Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer
title_full_unstemmed Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer
title_short Three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer
title_sort three-week schedule of irinotecan plus cisplatin in patients with previously untreated extensive-stage small-cell lung cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360764/
https://www.ncbi.nlm.nih.gov/pubmed/17133266
http://dx.doi.org/10.1038/sj.bjc.6603500
work_keys_str_mv AT hongys threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT leehr threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT parks threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT leesc threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT hwangig threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT parkbb threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT leej threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT ahnjs threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT ahnmj threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT limhy threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer
AT parkk threeweekscheduleofirinotecanpluscisplatininpatientswithpreviouslyuntreatedextensivestagesmallcelllungcancer