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Multicenter phase II study of trastuzumab in combination with capecitabine and oxaliplatin for advanced gastric cancer.
DC Field | Value | Language |
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dc.contributor.author | Ryu, MH | - |
dc.contributor.author | Yoo, C | - |
dc.contributor.author | Kim, JG | - |
dc.contributor.author | Ryoo, BY | - |
dc.contributor.author | Park, YS | - |
dc.contributor.author | Park, SR | - |
dc.contributor.author | Han, HS | - |
dc.contributor.author | Chung, IJ | - |
dc.contributor.author | Song, EK | - |
dc.contributor.author | Lee, KH | - |
dc.contributor.author | Kang, SY | - |
dc.contributor.author | Kang, YK | - |
dc.date.accessioned | 2017-06-07T01:14:04Z | - |
dc.date.available | 2017-06-07T01:14:04Z | - |
dc.date.issued | 2015 | - |
dc.identifier.issn | 0959-8049 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/14040 | - |
dc.description.abstract | BACKGROUND: Trastuzumab has been approved for use in combination with fluoropyrimidine plus cisplatin for the treatment of human epidermal growth factor receptor 2 (HER2)-positive advanced gastric cancer (AGC). Although capecitabine plus oxaliplatin (XELOX) is a standard first-line regimen for AGC, combination trastuzumab plus XELOX has not been studied.
METHODS: Patients with metastatic or unresectable HER2-positive AGC were diagnosed by either HER2 immunohistochemistry (IHC) 3+ or IHC 2+/fluorescence in-situ hybridisation (FISH)+ received intravenous trastuzumab (8mg/m(2) for first cycle and 6mg/m(2) for subsequent cycles on day 1) plus oral capecitabine (1000mg/m(2) twice daily on days 1-14) and intravenous oxaliplatin (130mg/m(2) on day 1), every 3 weeks. The primary end-point was the objective response rate, and secondary end-points included progression-free survival (PFS), overall survival (OS) and toxicity profiles. RESULTS: Fifty-five HER2-positive AGC patients were enrolled between August 2011 and February 2013. The median age was 57years (range=29-74). The confirmed objective response rate was 67% (95% confidence interval (CI)=54-80%). After a median follow-up period of 13.8 months (range=6.1-23.9), the median PFS and OS were 9.8 months (95% CI=7.0-12.6) and 21.0 months (95% CI=6.4-35.7), respectively. Frequently encountered grade 3-4 toxicities included neutropenia (18%), anaemia (11%), and peripheral neuropathy (11%). There was a treatment-related death caused by severe diarrhoea and complicated sepsis. CONCLUSION: Combination of trastuzumab and XELOX is well tolerated and highly effective in patients with HER2-positive AGC. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Antibodies, Monoclonal, Humanized | - |
dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols | - |
dc.subject.MESH | Capecitabine | - |
dc.subject.MESH | Deoxycytidine | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fluorouracil | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Organoplatinum Compounds | - |
dc.subject.MESH | Receptor, ErbB-2 | - |
dc.subject.MESH | Stomach Neoplasms | - |
dc.subject.MESH | Trastuzumab | - |
dc.title | Multicenter phase II study of trastuzumab in combination with capecitabine and oxaliplatin for advanced gastric cancer. | - |
dc.type | Article | - |
dc.identifier.pmid | 25661103 | - |
dc.identifier.url | https://linkinghub.elsevier.com/retrieve/pii/S0959-8049(15)00004-0 | - |
dc.contributor.affiliatedAuthor | 강, 석윤 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1016/j.ejca.2014.12.015 | - |
dc.citation.title | European journal of cancer (Oxford, England : 1990) | - |
dc.citation.volume | 51 | - |
dc.citation.number | 4 | - |
dc.citation.date | 2015 | - |
dc.citation.startPage | 482 | - |
dc.citation.endPage | 488 | - |
dc.identifier.bibliographicCitation | European journal of cancer (Oxford, England : 1990), 51(4). : 482-488, 2015 | - |
dc.identifier.eissn | 1879-0852 | - |
dc.relation.journalid | J009598049 | - |
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