Japanese Journal of Clinical Oncology Advance Access published online on July 26, 2006
Japanese Journal of Clinical Oncology, doi:10.1093/jjco/hyl062
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1 Thoracic Oncology Center, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan
* To whom correspondence should be addressed. Objective: The aim of this study was to evaluate the efficacy and toxicity of gemcitabine combined with irinotecan in patients with previously treated non-small-cell lung cancer (NSCLC). Methods: Patients who failed to respond to platinum-containing first-line chemotherapy were enrolled and treated with gemcitabine 1000 mg/m2 and irinotecan 150 mg/m2 on days 1 and 15. Cycles were repeated every 4 weeks. Results: Twenty-seven of 30 registered patients were evaluated. There were previous combination treatments of platinum and taxane regimens in 21 out of 27 patients, with 17 patients treated with carboplatin and paclitaxel and 4 patients treated with cisplatin or carboplatin and docetaxel. A total of 87 cycles was administered and the median number of cycles administered per patient was 3.5 cycles. Objective responses were observed in 5 out of 27 patients (18.5%). No severe hematologic and non-hematologic toxicities were observed (grade 3 leukopenia in 3 patients; grade 3 anemia in 3 patients; grade 3 thrombocytopenia in 2 patients; grade 3 diarrhea in 1 patient). The median survival time was 7.7 months and 1-year survival rate was 34.8%. Conclusion: Bi-weekly gemcitabine and irinotecan was well tolerated and had an acceptable response rate and a reasonable median survival time for patients with NSCLC who had previously been treated with platinum-based chemotherapy.
Received November 5, 2005
Accepted June 8, 2006
Original Article
Phase II Study of Combination Chemotherapy with Gemcitabine and Irinotecan in Patients with Advanced Non-Small-Cell Lung Cancer Previously Treated with Platinum-Containing Chemotherapy Regimens
Fumiyoshi Ohyanagi 1, Fumiko Taguchi 1, Takeshi Horai 1, Kazuo Kasahara 2, Yuichiro Takeda 3, Kazuhiko Shibata 4, Hiroki Shirosaki 5, and Makoto Nishio 1 *
2 Respiratory Medicine, Kanazawa University Hospital, Kanazawa, Japan
3 Department of Respiratory Medicine, International Medical Center of Japan, Tokyo, Japan
4 Department of Respiratory Medicine, Kouseiren Takaoka Hospital, Takaoka, Toyama, Japan
5 Department of Internal Medicine, Fukui Saiseikai Hospital, Fukui, Japan
Makoto Nishio, E-mail: mnishio{at}jfcr.or.jp
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