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Cited 15 time in webofscience Cited 16 time in scopus
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Salvage treatment with topotecan in patients with irinotecan-refractory small cell lung cancer

Authors
Park, Se HoonCho, Eun KyungKim, YujinKyung, Sun YoungAn, Chang HyeokLee, Sang PyoPark, Jeong WoongJeong, Sung HwanLee, Jae-IkChoi, Soo JinPark, JinnyShin, Dong BokLee, Jae Hoon
Issue Date
Nov-2008
Publisher
Springer Verlag
Keywords
small-cell lung cancer; refractory; chemotherapy; topotecan
Citation
Cancer Chemotherapy and Pharmacology, v.62, no.6, pp 1009 - 1014
Pages
6
Indexed
SCOPUS
Journal Title
Cancer Chemotherapy and Pharmacology
Volume
62
Number
6
Start Page
1009
End Page
1014
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/65719
DOI
10.1007/s00280-008-0690-1
ISSN
0344-5704
1432-0843
Abstract
Purpose Although the efficacy of topotecan as a second-line chemotherapy for small-cell lung cancer (SCLC) has been consistently demonstrated in phase II/III clinical trials, the choice of irinotecan as the first-line therapy prevented the use of evidence-based option. This pilot study was conducted to determine the activity and safety of topotecan in SCLC patients refractory to first-line therapy with irinotecan and platinum. Methods Patients with primary refractory (no response, or progression during or <= 90 days after last chemotherapy) SCLC after treatment with a combination of irinotecan and platinum, received topotecan 1.5 mg/m(2) per day as a 30-min infusion daily for 5 days, every 3 weeks. Results Of 17 eligible patients, ten patients were previously treated with irinotecan plus cisplatin and 7 were treated with irinotecan plus carboplatin. The median age was 68 years (range 44-75) and the median interval from the last chemotherapy was 50 days (range 21-89). A total of 33 chemotherapy cycles were delivered (median 2; range 1-5). All 17 patients discontinued therapy due to disease progression and 5 patients had progressive disease before second cycle. Toxic effects were mainly hematologic (grade >= 3 neutropenia in 65% of patients) and fatigue (grade 3 in 47%). In an intent-to-treat analysis, two (12%) patients had a confirmed partial response and two patients achieved stable disease. Median progression-free and overall survivals were 1.7 months (95% CI, 1.5-1.9) and 3.4 months (95% CI, 1.7-5.0), respectively. Conclusion Topotecan monotherapy for patients with irinotecan-refractory SCLC does not appear highly active but the observation of some responses merits further study in patients with chemosensitive disease.
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Park, Jinny
Ansan Hospital (Department of Medical Oncology and Hematology, Ansan Hospital)
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