The prognostic significance of KRAS and BRAF mutation status in Korean colorectal cancer patients
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Won, Daeyoun David
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Lee, Jae Im
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Catholic Univ Korea, Uijeongbu St Marys Hosp, Coll Med, Dept Surg, Seoul, South KoreaCatholic Univ Korea, Seoul St Marys Hosp, Coll Med, Dept Surg, Seoul, South Korea
Lee, Jae Im
[2
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Lee, In Kyu
[1
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Oh, Seong-Taek
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Catholic Univ Korea, Uijeongbu St Marys Hosp, Coll Med, Dept Surg, Seoul, South KoreaCatholic Univ Korea, Seoul St Marys Hosp, Coll Med, Dept Surg, Seoul, South Korea
Oh, Seong-Taek
[2
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Jung, Eun Sun
[3
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Lee, Sung Hak
[3
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[1] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, Dept Surg, Seoul, South Korea
[2] Catholic Univ Korea, Uijeongbu St Marys Hosp, Coll Med, Dept Surg, Seoul, South Korea
[3] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, Dept Hosp Pathol, 222 Banpo Daero, Seoul 06591, South Korea
Background: BRAF and KRAS mutations are well-established biomarkers in anti-EGFR therapy. However, the prognostic significance of these mutations is still being examined. We determined the prognostic value of BRAF and KRAS mutations in Korean colorectal cancer (CRC) patients. Methods: From July 2010 to September 2013, 1096 patients who underwent surgery for CRC at Seoul St. Mary's Hospital were included in the analysis. Resected specimens were examined for BRAF, KRAS, and microsatellite instability (MSI) status. All data were reviewed retrospectively. Results: Among 1096 patients, 401 (36.7%) had KRAS mutations and 44 (4.0%) had BRAF mutations. Of 83 patients, 77 (92.8%) had microsatellite stable (MSS) or MSI low (MSI-L) status while 6 (7.2%) patients had MSI high (MSI-H) status. Patients with BRAF mutation demonstrated a worse disease-free survival (DFS, HR 1.990, CI 1.080-3.660, P = 0. 02) and overall survival (OS, HR 3.470, CI 1.900-6.330, P < 0.0001). Regarding KRAS status, no significant difference was noted in DFS (P = 0.0548) or OS (P = 0.107). Comparing the MSS/MSI-L and MSI-H groups there were no significant differences in either DFS (P = 0.294) or OS (P = 0.557). Conclusions: BRAF mutation, rather than KRAS, was a significant prognostic factor in Korean CRC patients at both early and advanced stages. The subgroup analysis for MSI did not show significant differences in clinical outcome. BRAF should be included in future larger prospective biomarker studies on CRC.
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Department of Internal Medicine,Institute of Gastroenterology,Yonsei University College of Medicine,Seoul 120-752,South KoreaDepartment of Internal Medicine,Institute of Gastroenterology,Yonsei University College of Medicine,Seoul 120-752,South Korea
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Natl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Nakano, Shiori
Yamaji, Taiki
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Natl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Yamaji, Taiki
Shiraishi, Kouya
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Natl Canc Ctr, Div Genome Biol, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Shiraishi, Kouya
Hidaka, Akihisa
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Natl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Jikei Univ, Div Gastroenterol & Hepatol, Daisan Hosp, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Hidaka, Akihisa
Shimazu, Taichi
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Natl Canc Ctr Inst Canc Control, Div Behav Sci, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Shimazu, Taichi
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Kuchiba, Aya
Saito, Masahiro
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Hiraka Gen Hosp, Dept Diagnost Pathol, Yokote, Akita, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Saito, Masahiro
Kunishima, Fumihito
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Okinawa Prefecture Chubu Hosp, Dept Diagnost Pathol, Uruma, Okinawa, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Kunishima, Fumihito
Nakaza, Ryouji
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Nakagami Hosp, Dept Clin Lab, Okinawa, Okinawa, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Nakaza, Ryouji
Kohno, Takashi
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Natl Canc Ctr, Div Genome Biol, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Kohno, Takashi
Sawada, Norie
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Natl Canc Ctr Inst Canc Control, Div Cohort Res, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Sawada, Norie
Inoue, Manami
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Natl Canc Ctr Inst Canc Control, Div Prevent, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Inoue, Manami
Tsugane, Shoichiro
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Natl Canc Ctr Inst Canc Control, Div Cohort Res, Tokyo, Japan
Natl Inst Biomed Innovat Hlth & Nutr, Natl Inst Hlth & Nutr, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Tsugane, Shoichiro
Iwasaki, Motoki
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Natl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan
Natl Canc Ctr Inst Canc Control, Div Cohort Res, Tokyo, JapanNatl Canc Ctr Inst Canc Control, Div Epidemiol, Tokyo, Japan