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Outcomes of Third-Line Docetaxel-Based Chemotherapy in Advanced Gastric Cancer Who Failed Previous Oxaliplatin-Based and Irinotecan-Based Chemotherapies

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dc.contributor.authorLee, Min Jeong-
dc.contributor.authorHwang, In Gyu-
dc.contributor.authorJang, Joung-Soon-
dc.contributor.authorChoi, Jin Hwa-
dc.contributor.authorPark, Byeong-Bae-
dc.contributor.authorChang, Myung Hee-
dc.contributor.authorKim, Seung Tae-
dc.contributor.authorPark, Se Hoon-
dc.contributor.authorKang, Myoung Hee-
dc.contributor.authorKang, Jung Hun-
dc.date.accessioned2021-09-06T12:29:14Z-
dc.date.available2021-09-06T12:29:14Z-
dc.date.created2021-06-14-
dc.date.issued2012-12-
dc.identifier.issn1598-2998-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/106775-
dc.description.abstractPurpose Little is known about outcomes in the use of third-line chemotherapy in cases of advanced gastric cancer (AGC). The primary aim of this retrospective study was to evaluate outcomes of docetaxel-based chemotherapy in patients with AGC that progressed after both oxaliplatin-based and irinotecan-based regimens. Materials and Methods Eligible patients were those with AGC who had previous chemotherapy including fluoropyrimidine and oxaliplatin as well as fluoropyrimidine and irinotecan and who received subsequent docetaxel-based chemotherapy. Thirty-five patients were retrospectively recruited from 5 medical centers in Korea. Patients received either weekly or 3 weekly with docetaxel +/- cisplatin. Results Thirty-one out of 35 patients were evaluated for treatment response. A total of 94 cycles of chemotherapy (median, 2; range, 1 to 7) were administered. The overall response rate was 14.3%, and the disease control rate was 45.7%. The median progression-free survival (PFS) was 1.9 months (95% confidence interval [Cl], 1.1 to 2.7 months). The median overall survival (OS) was 3.6 months (95% Cl, 2.8 to 4.4 months). PFS and OS were significantly prolonged in patients of the Eastern Cooperative Oncology Group, with performance status of 0 or 1 in multivariate analysis (PFS: hazard ratio[HR], 0.411; 95% Cl, 0.195 to 0.868; p=0.020 and OS: HR, 0.390; 95% Cl, 0.184 to 0.826; p=0.014, respectively). Four of the 35 patients enrolled in the study died due to infection associated with neutropenia. Conclusion Our findings suggest that salvage docetaxel-based chemotherapy is a feasible treatment option for AGC patients with good performance status (PS), whereas chemotherapy for patients with poor PS (PS <= 2) should be undertaken with caution for those who previously failed oxaliplatin- and irinotecan-based regimens.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN CANCER ASSOCIATION-
dc.subjectSUPPORTIVE CARE-
dc.subjectCOMBINATION CHEMOTHERAPY-
dc.subject2ND-LINE CHEMOTHERAPY-
dc.subjectSALVAGE CHEMOTHERAPY-
dc.subjectPLUS-
dc.subjectFLUOROURACIL-
dc.subjectLEUCOVORIN-
dc.subjectSURVIVAL-
dc.subjectFOLFIRI-
dc.titleOutcomes of Third-Line Docetaxel-Based Chemotherapy in Advanced Gastric Cancer Who Failed Previous Oxaliplatin-Based and Irinotecan-Based Chemotherapies-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Seung Tae-
dc.identifier.doi10.4143/crt.2012.44.4.235-
dc.identifier.scopusid2-s2.0-84873972371-
dc.identifier.wosid000313303100003-
dc.identifier.bibliographicCitationCANCER RESEARCH AND TREATMENT, v.44, no.4, pp.235 - 241-
dc.relation.isPartOfCANCER RESEARCH AND TREATMENT-
dc.citation.titleCANCER RESEARCH AND TREATMENT-
dc.citation.volume44-
dc.citation.number4-
dc.citation.startPage235-
dc.citation.endPage241-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001724440-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusSUPPORTIVE CARE-
dc.subject.keywordPlusCOMBINATION CHEMOTHERAPY-
dc.subject.keywordPlus2ND-LINE CHEMOTHERAPY-
dc.subject.keywordPlusSALVAGE CHEMOTHERAPY-
dc.subject.keywordPlusPLUS-
dc.subject.keywordPlusFLUOROURACIL-
dc.subject.keywordPlusLEUCOVORIN-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusFOLFIRI-
dc.subject.keywordAuthorStomach neoplasms-
dc.subject.keywordAuthorDocetaxel-
dc.subject.keywordAuthorOxaliplatin-
dc.subject.keywordAuthorIrinotecan-
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