Bevacizumab-based treatment in colorectal cancer with a NRAS Q61K mutation

被引:5
|
作者
Janku, Filip [1 ]
Wheler, Jennifer J. [1 ]
Hong, David S. [1 ]
Kurzrock, Razelle [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Invest Canc Therapeut, Phase Clin Trials Program 1, Houston, TX 77030 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
关键词
NRAS mutation; Colorectal cancer; Bevacizumab; Q61K; ENDOTHELIAL GROWTH-FACTOR; HISTONE DEACETYLASES; CELL-SURVIVAL; N-RAS; COMBINATION; KINASE; CHEMOTHERAPY; ANGIOGENESIS; INHIBITOR; BRAF;
D O I
10.1007/s11523-013-0266-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite development of new therapies, metastatic colorectal cancer (mCRC) largely remains an incurable disease. Approximately 2-6 % of colorectal cancers harbor NRAS mutations. The anti-VEGF antibody bevacizumab is a backbone of most therapeutic regimens; however, biomarkers predicting its activity are not known. We report two cases of mCRC with a Q61K NRAS mutation that had a favorable response to bevacizumab and the histone deacetylase inhibitor valproic acid. In contrast, none of ten patients with wild-type NRAS or unknown NRAS status and mutated KRAS (NRAS and KRAS mutations are mutually exclusive) responded to the same regimen. These results suggest that NRAS mutation merits further investigation as a potential biomarker predicting the efficacy of bevacizumab-based treatment.
引用
收藏
页码:183 / 188
页数:6
相关论文
共 50 条
  • [1] Bevacizumab-based treatment in colorectal cancer with a NRAS Q61K mutation
    Filip Janku
    Jennifer J. Wheler
    David S. Hong
    Razelle Kurzrock
    Targeted Oncology, 2013, 8 : 183 - 188
  • [2] Giant congenital melanocytic naevus caused by NRAS Q61K mosaicism
    Thielmann, Carl M.
    Kampmeier, Antje
    Kuechler, Alma
    Zenker, Martin
    Wieland, Ilse
    Matull, Johanna
    Krefting, Frederik
    Griewank, Klaus
    Hadaschik, Eva
    JEADV CLINICAL PRACTICE, 2022, 1 (04): : 416 - 419
  • [3] Immunological Effects of Bevacizumab-Based Treatment in Metastatic Colorectal Cancer
    Manzoni, M.
    Rovati, B.
    Ronzoni, M.
    Loupakis, F.
    Mariucci, S.
    Ricci, V.
    Gattoni, E.
    Salvatore, L.
    Tinelli, C.
    Villa, E.
    Danova, M.
    ONCOLOGY, 2010, 79 (3-4) : 187 - 196
  • [4] Combined inhibition of MEK and mTOR pathways is effective in NRAS Q61K mutant small cell lung cancer
    Ogino, Atsuko
    Lin, Mika
    Gokhale, Prafulla C.
    Wilkens, Margaret K.
    Choi, Jihyun
    Calles, Antonio
    Xu, Man
    Capelletti, Marzia
    Oxnard, Geoffrey
    Gray, Nathanael S.
    Kirschmeier, Paul
    Janne, Pasi A.
    CANCER RESEARCH, 2018, 78 (13)
  • [5] Rapid progression to AML in a patient with germline GATA2 mutation and acquired NRAS Q61K mutation (vol 12, 100176, 2019)
    McReynolds, Lisa J.
    LEUKEMIA RESEARCH REPORTS, 2022, 17
  • [6] Crystal structure of NRAS Q61K with a ligand-induced pocket near switch II
    Gebregiworgis, Teklab
    Chan, Jonathan Yui-Lai
    Kuntz, Douglas A.
    Prive, Gilbert G.
    Marshall, Christopher B.
    Ikura, Mitsuhiko
    EUROPEAN JOURNAL OF CELL BIOLOGY, 2024, 103 (02)
  • [7] An Acquired NRAS Q61K Mutation in BRAF V600E-Mutant Lung Adenocarcinoma Resistant to Dabrafenib Plus Trametinib
    Abravanel, Daniel L.
    Nishino, Mizuki
    Sholl, Lynette M.
    Ambrogio, Chiara
    Awad, Mark M.
    JOURNAL OF THORACIC ONCOLOGY, 2018, 13 (08) : E131 - E133
  • [8] Rapid progression to AML in a patient with germline GATA2 mutation and acquired NRAS Q61K mutation (vol 12C, 100176, 2019)
    Lu, S. Y.
    LEUKEMIA RESEARCH REPORTS, 2022, 17
  • [9] Bevacizumab-Based Therapies in the First-Line Treatment of Metastatic Colorectal Cancer
    Strickler, John H.
    Hurwitz, Herbert I.
    ONCOLOGIST, 2012, 17 (04): : 513 - 524
  • [10] The effects of dasatinib in KIT L579P and NRAS Q61K mutant canine melanoma cells
    Lu, Lu-Ping
    Lin, Chen-Si
    Liao, Albert Taiching
    CANCER RESEARCH, 2015, 75