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Belotecan, new camptothecin analogue, is active in patients with small-cell lung cancer: results of a multicenter early phase II study

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dc.contributor.authorLee, D. H.-
dc.contributor.authorKim, S. -W.-
dc.contributor.authorSuh, C.-
dc.contributor.authorLee, J. -S.-
dc.contributor.authorLee, J. H.-
dc.contributor.authorLee, S-J.-
dc.contributor.authorRyoo, B. Y.-
dc.contributor.authorPark, K.-
dc.contributor.authorKim, J. S.-
dc.contributor.authorHeo, D. S.-
dc.contributor.authorKim, N. K.-
dc.date.accessioned2021-09-09T12:50:11Z-
dc.date.available2021-09-09T12:50:11Z-
dc.date.created2021-06-15-
dc.date.issued2008-01-
dc.identifier.issn0923-7534-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/124458-
dc.description.abstractBackground: Belotecan (Camtobell (R), Chong Keun Dang Corp, Seoul, Korea; CKD602) is a new camptothecin analogue. This study aimed to investigate the safety and efficacy of single-agent belotecan for small-cell lung cancer (SCLC). Patients and methods: Twenty-seven patients with chemotherapy-naive or chemosensitive SCLC were treated with belotecan 0.5 mg/m(2)/day on days 1-5 of a 3-week cycle. All 27 patients were assessable for toxicity, and 21 patients assessable for response. Results: Nine patients (42.9%) showed objective tumor responses including one complete response; seven (63.6%) in 11 chemotherapy-naive patients; and two (20.0%) in 10 chemosensitive patients. With a median follow-up of 5 years, median progression-free and survival time for chemotherapy-naive patients were 4.8 months and 11.9 months, respectively, while the corresponding values for chemosensitive patients were 3.3 months and 10.5 months, respectively. The most common toxicity was neutropenia. Conclusion: Belotecan was active in SCLC patients as a single agent, warranting further investigations of belotecan in combination with platinum or other active agents.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherOXFORD UNIV PRESS-
dc.subjectMETASTATIC COLORECTAL-CANCER-
dc.subjectFLUOROURACIL FAILURE-
dc.subjectRANDOMIZED-TRIAL-
dc.subjectIRINOTECAN-
dc.subjectTOPOTECAN-
dc.subjectDISEASE-
dc.subjectCHEMOTHERAPY-
dc.subjectCARCINOMA-
dc.subjectCISPLATIN-
dc.subjectETOPOSIDE-
dc.titleBelotecan, new camptothecin analogue, is active in patients with small-cell lung cancer: results of a multicenter early phase II study-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, J. S.-
dc.identifier.doi10.1093/annonc/mdm437-
dc.identifier.scopusid2-s2.0-37849041674-
dc.identifier.wosid000253176400019-
dc.identifier.bibliographicCitationANNALS OF ONCOLOGY, v.19, no.1, pp.123 - 127-
dc.relation.isPartOfANNALS OF ONCOLOGY-
dc.citation.titleANNALS OF ONCOLOGY-
dc.citation.volume19-
dc.citation.number1-
dc.citation.startPage123-
dc.citation.endPage127-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusMETASTATIC COLORECTAL-CANCER-
dc.subject.keywordPlusFLUOROURACIL FAILURE-
dc.subject.keywordPlusRANDOMIZED-TRIAL-
dc.subject.keywordPlusIRINOTECAN-
dc.subject.keywordPlusTOPOTECAN-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordPlusCISPLATIN-
dc.subject.keywordPlusETOPOSIDE-
dc.subject.keywordAuthorbelotecan-
dc.subject.keywordAuthorsingle agent-
dc.subject.keywordAuthorsmall-cell lung cancer-
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