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Oxaliplatin (3 months v 6 months) With 6 Months of Fluoropyrimidine as Adjuvant Therapy in Patients With Stage II/III Colon Cancer: KCSG CO09-07

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dc.contributor.author신상준-
dc.contributor.author안중배-
dc.date.accessioned2023-03-21T07:21:00Z-
dc.date.available2023-03-21T07:21:00Z-
dc.date.issued2022-11-
dc.identifier.issn0732-183X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/193324-
dc.description.abstractPurpose: The combination of oxaliplatin and fluoropyrimidine for 6 months is one of the standard options for adjuvant therapy for high-risk stage II and III colorectal cancers (CRCs). The optimal duration of oxaliplatin to diminish neurotoxicity without compromising efficacy needs to be clarified. Patients and methods: This open-label, randomized, phase III, noninferiority trial randomly assigned patients with high-risk stage II and III CRC to 3 and 6 months of oxaliplatin with 6 months of fluoropyrimidine groups (3- and 6-month arms, respectively). The primary end point was disease-free survival (DFS), and the noninferiority margin was a hazard ratio (HR) of 1.25. Results: In total, 1,788 patients were randomly assigned to the 6-month (n = 895) and 3-month (n = 893) arms, and 83.6% in the 6-month arm and 85.7% in the 3-month arm completed the treatment. The neuropathy rates with any grade were higher in the 6-month arm than in the 3-month arm (69.5% v 58.3%; P < .0001). The 3-year DFS rates were 83.7% and 84.7% in the 6-month and 3-month arms, respectively, with an HR of 0.953 (95% CI, 0.769 to 1.180; test for noninferiority, P = .0065) within the noninferiority margin. Among patients with stage III CRC treated by capecitabine plus oxaliplatin, the 3-year DFS of the 3-month arm was noninferior as compared with that of the 6-month arm with an HR of 0.713 (95% CI, 0.530 to 0.959; P = .0009). However, among patients with high-risk stage II and stage III CRC treated by infusional fluorouracil, leucovorin, and oxaliplatin, the noninferiority of the 3-month arm compared with the 6-month arm was not proven. Conclusion: This study suggests that adding 3 months of oxaliplatin to 6 months of capecitabine could be considered an alternative adjuvant treatment for stage III CRC (ClinicalTrials.gov identifier: NCT01092481).-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherAmerican Society of Clinical Oncology-
dc.relation.isPartOfJOURNAL OF CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols / therapeutic use-
dc.subject.MESHCapecitabine / therapeutic use-
dc.subject.MESHChemotherapy, Adjuvant-
dc.subject.MESHColonic Neoplasms* / drug therapy-
dc.subject.MESHColonic Neoplasms* / pathology-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFluorouracil / therapeutic use-
dc.subject.MESHHumans-
dc.subject.MESHLeucovorin / therapeutic use-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHOrganoplatinum Compounds* / therapeutic use-
dc.subject.MESHOxaliplatin* / therapeutic use-
dc.titleOxaliplatin (3 months v 6 months) With 6 Months of Fluoropyrimidine as Adjuvant Therapy in Patients With Stage II/III Colon Cancer: KCSG CO09-07-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorSeung Tae Kim-
dc.contributor.googleauthorSun Young Kim-
dc.contributor.googleauthorJeeyun Lee-
dc.contributor.googleauthorSeong Hyeon Yun-
dc.contributor.googleauthorHee Cheol Kim-
dc.contributor.googleauthorWoo Yong Lee-
dc.contributor.googleauthorTae Won Kim-
dc.contributor.googleauthorYong Sang Hong-
dc.contributor.googleauthorSeok-Byung Lim-
dc.contributor.googleauthorJi Yeon Baek-
dc.contributor.googleauthorJae Hwan Oh-
dc.contributor.googleauthorJoong Bae Ahn-
dc.contributor.googleauthorSang Joon Shin-
dc.contributor.googleauthorSae-Won Han-
dc.contributor.googleauthorSeong Geun Kim-
dc.contributor.googleauthorSeok Yun Kang-
dc.contributor.googleauthorSun Jin Sym-
dc.contributor.googleauthorDae Young Zang-
dc.contributor.googleauthorYeul Hong Kim-
dc.contributor.googleauthorIn Sil Choi-
dc.contributor.googleauthorJung Hun Kang-
dc.contributor.googleauthorMin-Ji Kim-
dc.contributor.googleauthorYoung Suk Park-
dc.identifier.doi10.1200/JCO.21.02962-
dc.contributor.localIdA02105-
dc.contributor.localIdA02262-
dc.relation.journalcodeJ01331-
dc.identifier.eissn1527-7755-
dc.identifier.pmid35772045-
dc.identifier.urlhttps://ascopubs.org/doi/10.1200/JCO.21.02962-
dc.contributor.alternativeNameShin, Sang Joon-
dc.contributor.affiliatedAuthor신상준-
dc.contributor.affiliatedAuthor안중배-
dc.citation.volume40-
dc.citation.number33-
dc.citation.startPage3868-
dc.citation.endPage3877-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL ONCOLOGY, Vol.40(33) : 3868-3877, 2022-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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