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Combined Microsatellite Instability and BRAF Gene Status As Biomarkers for Adjuvant Chemotherapy in Stage III Colorectal Cancer
被引:25
|作者:
Ooki, Akira
[1
]
Akagi, Kiwamu
[2
]
Yatsuoka, Toshimasa
[3
]
Asayama, Masako
[1
]
Hara, Hiroki
[1
]
Takahashi, Akemi
[2
]
Kakuta, Miho
[2
]
Nishimura, Yoji
[3
]
Yamaguchi, Kensei
[1
]
机构:
[1] Saitama Canc Ctr, Dept Gastroenterol, Ina, Saitama 3620806, Japan
[2] Saitama Canc Ctr, Div Mol Diag & Canc Prevent, Ina, Saitama 3620806, Japan
[3] Saitama Canc Ctr, Dept Surg Gastroenterol, Ina, Saitama 3620806, Japan
关键词:
MSI;
BRAF;
colorectal cancer;
adjuvant chemotherapy;
DEFECTIVE MISMATCH REPAIR;
COLON-CANCER;
V600E MUTATION;
FLUOROURACIL;
LEUCOVORIN;
OXALIPLATIN;
SURVIVAL;
CARCINOMA;
EFFICACY;
THERAPY;
D O I:
10.1002/jso.23755
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BackgroundThe clinical relevance of combined microsatellite instability (MSI) and BRAF status for adjuvant treatment in stage III colorectal cancer (CRC) remains elusive. MethodsIn 405 patients with curatively resected stage III CRC, the prognostic value of combined MSI and BRAF status was assessed in four groups, as follows: high-levels of microsatellite instability (MSI-H) and BRAF-wild type, MSI-H and BRAF-mutation, microsatellite stable (MSS) and BRAF-wild type, and MSS and BRAF-mutation. ResultsCombined MSI and BRAF status provided significant prognostic stratification of disease-free survival (DFS), and was independently associated with worse DFS. The MSI-H and BRAF-wild type group had similar outcomes to stage II CRC patients, despite no benefit from 5-FU monotherapy. Further, patients in the MSS and BRAF-wild type group with stage IIIA CRC had favorable outcomes to 5-FU monotherapy, similar to those with stage II CRC. In contrast, 5-FU monotherapy was insufficient among patients in the MSS and BRAF-wild type group with stage IIIB or IIIC CRC or patients in the MSS and BRAF-mutation group with stage III CRC. ConclusionsThe combination of MSI and BRAF status serves as both a prognostic and predictive marker and may provide much-needed guidance during the planning of therapeutic strategies. J. Surg. Oncol. 2014; 110:982-988. (c) 2014 Wiley Periodicals, Inc.
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页码:982 / 988
页数:7
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