Epidermal growth factor receptor-targeted treatment strategies in advanced pancreatic cancer: Is K-RAS mutational testing ready for prime time?

被引:0
|
作者
Bauernhofer T. [1 ]
机构
[1] Division of Oncology, Department of Internal Medicine, Medical University Graz, A-8036 Graz
关键词
DNA mutational analysis; Erlotinib; Gemcitabine; Outcome; Pancreatic neoplasms; Treatment response;
D O I
10.1007/s12254-011-0302-3
中图分类号
学科分类号
摘要
The combination of gemcitabine with erlotinib is viewed as one standard in the treatment of patients with advanced pancreatic cancer. However, the magnitude of the survival benefit of the combination therapy compared to single agent gemcitabine is relatively small. Whether this statistically significant survival benefit translates to a relevant clinical benefit of the combined treatment in view of increased toxicity and costs is still a matter of debate. Consequently, there has been great interest in identifying molecular biomarkers predictive for response and survival benefit from EGFR-targeted agents in advanced pancreatic cancer. No data have been published up to now concerning the value of K-RAS mutations in pancreatic cancer as a predictive marker for lack of response to EGFR targeted agents. Nevertheless, the first prospective evaluation of K-RAS status and response to erlotinib in combination with either gemcitabine or capecitabine suggest a significant improvement of overall survival only for patients with K-RAS wild type tumors suggesting a possible role of K-RAS mutational status as predictive marker in pancreatic cancer. © Springer-Verlag 2011.
引用
收藏
页码:257 / 259
页数:2
相关论文
共 50 条
  • [2] Understanding the Predictive Role of K-ras for Epidermal Growth Factor Receptor-Targeted Therapies in Colorectal Cancer
    Ramos, Francisco Javier
    Macarulla, Teresa
    Capdevila, Jaume
    Elez, Elena
    Tabernero, Josep
    CLINICAL COLORECTAL CANCER, 2008, 7 : S52 - S57
  • [3] Treatment of pancreatic cancer with epidermal growth factor receptor-targeted therapy
    Faller, Bryan A.
    Burtness, Barbara
    BIOLOGICS-TARGETS & THERAPY, 2009, 3 : 419 - 428
  • [4] Epidermal growth factor receptor-targeted therapy for pancreatic cancer
    Xiong, HQ
    Abbruzzese, JL
    SEMINARS IN ONCOLOGY, 2002, 29 (05) : 31 - 37
  • [5] Epidermal growth factor receptor-targeted therapy for pancreatic cancer
    Papageorgio, Chris
    Perry, Michael C.
    CANCER INVESTIGATION, 2007, 25 (07) : 647 - 657
  • [6] Epidermal growth factor receptor-targeted treatment for advanced colorectal carcinoma
    Venook, AP
    CANCER, 2005, 103 (12) : 2435 - 2446
  • [7] Treatment Paradigms With Epidermal Growth Factor Receptor-Targeted Therapies in Colorectal Cancer
    Stein, Stacey
    Cohen, Deirdre J.
    Hochster, Howard S.
    CLINICAL COLORECTAL CANCER, 2010, 9 : S44 - S50
  • [8] Epidermal growth factor receptor-targeted therapy in colorectal cancer
    O'Dwyer, PJ
    Benson, AB
    SEMINARS IN ONCOLOGY, 2002, 29 (05) : 10 - 17
  • [9] Epidermal growth factor receptor-targeted therapy in colorectal cancer
    Xu, WeiDong
    Jing, HuaYong
    Zhang, FuLi
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2016, 21 : 410 - 418
  • [10] Mutations in epidermal growth factor receptor and K-ras in Chinese patients with colorectal cancer
    Zuo Yunxia
    Cao Jun
    Zhu Guanshan
    Lu Yachao
    Zhou Xueke
    Li Jin
    BMC MEDICAL GENETICS, 2010, 11