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.
引用
收藏
页码:982 / 988
页数:7
相关论文
共 50 条
  • [41] Final report of KSCC0803: feasibility study of capecitabine as adjuvant chemotherapy for stage III colon cancer in Japan
    Minami, Kazuhito
    Morita, Masaru
    Emi, Yasunori
    Okamoto, Masahiro
    Tanaka, Eiji
    Nagata, Shigeyuki
    Touyama, Tetsuo
    Ohgaki, Kippei
    Tanaka, Takaho
    Okumura, Hiroshi
    Suenaga, Toyokuni
    Tokunaga, Shoji
    Oki, Eiji
    Kakeji, Yoshihiro
    Akagi, Yoshito
    Baba, Hideo
    Natsugoe, Shoji
    Maehara, Yoshihiko
    INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2017, 22 (03) : 505 - 510
  • [42] Timing of adjuvant chemotherapy and its relation to survival among patients with stage III colon cancer
    Bos, A. C. R. K.
    van Erning, F. N.
    van Gestel, Y. R. B. M.
    Creemers, G. J. M.
    Punt, C. J. A.
    van Oijen, M. G. H.
    Lemmens, V. E. P. P.
    EUROPEAN JOURNAL OF CANCER, 2015, 51 (17) : 2553 - 2561
  • [43] Jagged-1 Expression Level Is Correlated With Recurrence of Stage III Colorectal Cancer in Patients Receiving Adjuvant Chemotherapy
    Kim, Hong-Beum
    Lee, Seul-Bi
    Kim, Seong-Jung
    Lee, Hee-Jeong
    Park, Sang-Gon
    ANTICANCER RESEARCH, 2021, 41 (09) : 4645 - 4650
  • [44] Early liver metastases after "failure" of adjuvant chemotherapy for stage III colorectal cancer: is there a role for additional adjuvant therapy?
    Boerner, Thomas
    Zambirinis, Constantinos
    Gagniere, Johan
    Chou, Joanne F.
    Gonen, Mithat
    Kemeny, Nancy E.
    Cercek, Andrea
    Connell, Louise C.
    Kingham, Thomas P.
    Allen, Peter J.
    Balachandran, Vinod P.
    Drebin, Jeffrey
    Jarnagin, William R.
    D'Angelica, Michael, I
    HPB, 2021, 23 (04) : 601 - 608
  • [45] Lower serum CA125 level, negative vascular invasion, and wild BRAF were strongly associated with better 2-year disease-free survival in patients with stage III colorectal cancer who received adjuvant chemotherapy
    Chang, Shu-Jian
    Ge, Xiao-Song
    Xu, Zhen-Yu
    Qi, Xiao-Wei
    Chen, Xiao-Ping
    CANCER BIOMARKERS, 2018, 22 (01) : 161 - 168
  • [46] Clinicopathological predictors of benefit from adjuvant chemotherapy for stage C colorectal cancer: Microsatellite unstable cases benefit
    Thomas, Michelle L.
    Hewett, Peter J.
    Ruszkiewicz, Andrew R.
    Moore, James W. E.
    ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2015, 11 (04) : 343 - 351
  • [47] Methylation and microsatellite status and recurrence following adjuvant FOLFOX in colorectal cancer
    Han, Sae-Won
    Lee, Hyun-Jung
    Bae, Jeong Mo
    Cho, Nam-Yun
    Lee, Kyung-Hun
    Kim, Tae-Yong
    Oh, Do-Youn
    Im, Seock-Ah
    Bang, Yung-Jue
    Jeong, Seung-Yong
    Park, Kyu Joo
    Park, Jae-Gahb
    Kang, Gyeong Hoon
    Kim, Tae-You
    INTERNATIONAL JOURNAL OF CANCER, 2013, 132 (09) : 2209 - 2216
  • [48] Prognostic Impact of Microsatellite Instability in Colorectal Cancer Patients Treated with Adjuvant FOLFOX
    Des Guetz, G.
    Lecaille, C.
    Mariani, P.
    Bennamoun, M.
    Uzzan, B.
    Nicolas, P.
    Boisseau, A.
    Sastre, X.
    Cucherousset, J.
    Lagorce, C.
    Schischmanoff, P. O.
    Morere, J. F.
    ANTICANCER RESEARCH, 2010, 30 (10) : 4297 - 4301
  • [49] Correlation between microsatellite instability and RAS gene mutation and stage III colorectal cancer
    Niu, Wenbo
    Wang, Guiying
    Feng, Jun
    Li, Zheng
    Li, Chenhui
    Shan, Baoen
    ONCOLOGY LETTERS, 2019, 17 (01) : 332 - 338
  • [50] Factors associated with delayed time to adjuvant chemotherapy in stage III colon cancer
    Chan, A.
    Woods, R.
    Kennecke, H.
    Gill, S.
    CURRENT ONCOLOGY, 2014, 21 (04) : 181 - 186