Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer
Objective. The goal of this study was to evaluate the efficacy and tolerability of irinotecan plus cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer. Methods. Chemotherapy-naive patients with metastatic or recurrent disease and at least one measurable tumor site receive...
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2014
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th-cmuir.6653943832-31122014-08-30T02:25:47Z Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer Chitapanarux I. Tonusin A. Sukthomya V. Charuchinda C. Pukanhapan N. Lorvidhaya V. Objective. The goal of this study was to evaluate the efficacy and tolerability of irinotecan plus cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer. Methods. Chemotherapy-naive patients with metastatic or recurrent disease and at least one measurable tumor site received irinotecan (60 mg/m2 IV infusion over 90 min) on Days 1, 8, and 15, followed by cisplatin (60 mg/m2 IV over 90 min) on Day 1, every 28 days for a maximum of six cycles. Results. Thirty patients were included in the response and toxicity analysis. The median age was 45 years (34-65). Nineteen patients had metastatic disease, 6 presented with locally recurrent disease, and 5 presented with locally recurrent plus metastatic disease. Seven patients were stage IVB at diagnosis. There were 2 complete and 18 partial responses and overall response rate was 66.7% (95% confidence interval: 47-85%). Stable disease was observed in 2 patients (6.7%) and progression in 8 (26.7%). Median time to relapse was 13.4 months, with a median survival time of 16.9 months. One-year disease-free survival and overall survival were 26.7 and 65.1%, respectively. Dose-limiting toxicity was observed in 4 patients (13.3%) with grade 3 renal toxicity. Nine patients (30%) developed grade 3 neutropenia, and only grade 1-2 acute and late diarrhea were observed in 20 and 40%, respectively. A patient developed pancolitis after the sixth cycle. There were no chemotherapy-related deaths. Conclusion. The combination of irinotecan and cisplatin is a clinically active regimen for metastatic and/or recurrent cervical cancer with acceptable tolerability. © 2003 Elsevier Science (USA). All rights reserved. 2014-08-30T02:25:47Z 2014-08-30T02:25:47Z 2003 Article 00908258 10.1016/S0090-8258(03)00174-4 12798702 GYNOA http://www.scopus.com/inward/record.url?eid=2-s2.0-0037498599&partnerID=40&md5=cbad447c75d91093ef9e07786e05f916 http://www.ncbi.nlm.nih.gov/pubmed/12798702 http://cmuir.cmu.ac.th/handle/6653943832/3112 English |
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Objective. The goal of this study was to evaluate the efficacy and tolerability of irinotecan plus cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer. Methods. Chemotherapy-naive patients with metastatic or recurrent disease and at least one measurable tumor site received irinotecan (60 mg/m2 IV infusion over 90 min) on Days 1, 8, and 15, followed by cisplatin (60 mg/m2 IV over 90 min) on Day 1, every 28 days for a maximum of six cycles. Results. Thirty patients were included in the response and toxicity analysis. The median age was 45 years (34-65). Nineteen patients had metastatic disease, 6 presented with locally recurrent disease, and 5 presented with locally recurrent plus metastatic disease. Seven patients were stage IVB at diagnosis. There were 2 complete and 18 partial responses and overall response rate was 66.7% (95% confidence interval: 47-85%). Stable disease was observed in 2 patients (6.7%) and progression in 8 (26.7%). Median time to relapse was 13.4 months, with a median survival time of 16.9 months. One-year disease-free survival and overall survival were 26.7 and 65.1%, respectively. Dose-limiting toxicity was observed in 4 patients (13.3%) with grade 3 renal toxicity. Nine patients (30%) developed grade 3 neutropenia, and only grade 1-2 acute and late diarrhea were observed in 20 and 40%, respectively. A patient developed pancolitis after the sixth cycle. There were no chemotherapy-related deaths. Conclusion. The combination of irinotecan and cisplatin is a clinically active regimen for metastatic and/or recurrent cervical cancer with acceptable tolerability. © 2003 Elsevier Science (USA). All rights reserved. |
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Chitapanarux I. Tonusin A. Sukthomya V. Charuchinda C. Pukanhapan N. Lorvidhaya V. |
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Chitapanarux I. Tonusin A. Sukthomya V. Charuchinda C. Pukanhapan N. Lorvidhaya V. Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer |
author_facet |
Chitapanarux I. Tonusin A. Sukthomya V. Charuchinda C. Pukanhapan N. Lorvidhaya V. |
author_sort |
Chitapanarux I. |
title |
Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer |
title_short |
Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer |
title_full |
Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer |
title_fullStr |
Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer |
title_full_unstemmed |
Phase II clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer |
title_sort |
phase ii clinical study of irinotecan and cisplatin as first-line chemotherapy in metastatic or recurrent cervical cancer |
publishDate |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-0037498599&partnerID=40&md5=cbad447c75d91093ef9e07786e05f916 http://www.ncbi.nlm.nih.gov/pubmed/12798702 http://cmuir.cmu.ac.th/handle/6653943832/3112 |
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1681419986962219008 |