Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer

Objective: To assess the activity and toxicity of cisplatin and irinotecan alternating with docetaxel in patients with advanced non-small cell lung cancer (NSCLC). Material and Method: Eligibility included chemo-naïve stage IIIB with malignant effusion and stage IV NSCLC patients with measurable dis...

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Main Authors: Charoentum C., Thongprasert S., Chewasakulyong B., Euathrongchit J., Sorraritchingchai S., Munprakan S.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-37149053450&partnerID=40&md5=084d5a357dc486f92b8f7b40f356ff89
http://www.ncbi.nlm.nih.gov/pubmed/18181342
http://cmuir.cmu.ac.th/handle/6653943832/2115
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-21152014-08-30T02:00:29Z Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer Charoentum C. Thongprasert S. Chewasakulyong B. Euathrongchit J. Sorraritchingchai S. Munprakan S. Objective: To assess the activity and toxicity of cisplatin and irinotecan alternating with docetaxel in patients with advanced non-small cell lung cancer (NSCLC). Material and Method: Eligibility included chemo-naïve stage IIIB with malignant effusion and stage IV NSCLC patients with measurable disease and a good performance status. Twenty-four patients were enrolled into the present study. There were 19 males and 5 females with a median age of 58.5 years and the median performance status was 1. Ninety-six percent had stage IV disease. These patients received cisplatin at 80 mg/ m2 and irinotecan at 200 mg/m2 on day 1, followed by docetaxel at 75 mg/m2 on day 22, in 6-week cycle for a maximum of 3 cycles. Results: Eight out of twenty-two evaluable patients obtained a partial response (36%). The median time to tumor progression was 6 months. The median survival time and 1-year survival rate were 10.4 months and 45% respectively. The most frequent severe toxicities were neutropenia, anemia, and diarrhea. Febrile neutropenia occurred in four patients (16%), and was the cause of treatment-related deaths in two (8%). Other nonhematologic toxicities were mild including nausea, vomiting, and skin rash. Conclusion: Alternating cisplatin and irinotecan with docetaxel, as used in the present study was feasible and demonstrated encouraging efficacy in patients with non-small cell lung cancer. However, this approach appears to be more toxic, especially in myelosuppression, than in previous reports of the sequential use of the similar agents. 2014-08-30T02:00:29Z 2014-08-30T02:00:29Z 2007 Article 01252208 18181342 JMTHB http://www.scopus.com/inward/record.url?eid=2-s2.0-37149053450&partnerID=40&md5=084d5a357dc486f92b8f7b40f356ff89 http://www.ncbi.nlm.nih.gov/pubmed/18181342 http://cmuir.cmu.ac.th/handle/6653943832/2115 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Objective: To assess the activity and toxicity of cisplatin and irinotecan alternating with docetaxel in patients with advanced non-small cell lung cancer (NSCLC). Material and Method: Eligibility included chemo-naïve stage IIIB with malignant effusion and stage IV NSCLC patients with measurable disease and a good performance status. Twenty-four patients were enrolled into the present study. There were 19 males and 5 females with a median age of 58.5 years and the median performance status was 1. Ninety-six percent had stage IV disease. These patients received cisplatin at 80 mg/ m2 and irinotecan at 200 mg/m2 on day 1, followed by docetaxel at 75 mg/m2 on day 22, in 6-week cycle for a maximum of 3 cycles. Results: Eight out of twenty-two evaluable patients obtained a partial response (36%). The median time to tumor progression was 6 months. The median survival time and 1-year survival rate were 10.4 months and 45% respectively. The most frequent severe toxicities were neutropenia, anemia, and diarrhea. Febrile neutropenia occurred in four patients (16%), and was the cause of treatment-related deaths in two (8%). Other nonhematologic toxicities were mild including nausea, vomiting, and skin rash. Conclusion: Alternating cisplatin and irinotecan with docetaxel, as used in the present study was feasible and demonstrated encouraging efficacy in patients with non-small cell lung cancer. However, this approach appears to be more toxic, especially in myelosuppression, than in previous reports of the sequential use of the similar agents.
format Article
author Charoentum C.
Thongprasert S.
Chewasakulyong B.
Euathrongchit J.
Sorraritchingchai S.
Munprakan S.
spellingShingle Charoentum C.
Thongprasert S.
Chewasakulyong B.
Euathrongchit J.
Sorraritchingchai S.
Munprakan S.
Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer
author_facet Charoentum C.
Thongprasert S.
Chewasakulyong B.
Euathrongchit J.
Sorraritchingchai S.
Munprakan S.
author_sort Charoentum C.
title Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer
title_short Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer
title_full Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer
title_fullStr Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer
title_full_unstemmed Phase II study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer
title_sort phase ii study of cisplatin combined to irinotecan administered alternatingly with docetaxel in advanced non-small cell lung cancer
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-37149053450&partnerID=40&md5=084d5a357dc486f92b8f7b40f356ff89
http://www.ncbi.nlm.nih.gov/pubmed/18181342
http://cmuir.cmu.ac.th/handle/6653943832/2115
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