KRAS Testing and Epidermal Growth Factor Receptor Inhibitor Treatment for Colorectal Cancer in Community Settings

被引:19
|
作者
Webster, Jennifer [1 ]
Kauffman, Tia L. [1 ]
Feigelson, Heather Spencer [2 ]
Pawloski, Pamala A. [3 ]
Onitilo, Adedayo A. [4 ,5 ]
Potosky, Arnold L. [6 ]
Cross, Deanna [4 ]
Meier, Paul R. [7 ]
Mirabedi, Anousheh S. [8 ]
Delate, Thomas [2 ]
Daida, Yihe [9 ]
Williams, Andrew E. [9 ]
Alexander, Gwen L. [7 ]
McCarty, Catherine A. [4 ,10 ]
Honda, Stacey [9 ]
Kushi, Lawrence H. [8 ]
Goddard, Katrina A. B. [1 ]
机构
[1] Kaiser Permanente NW, Ctr Hlth Res, Portland, OR 97227 USA
[2] Kaiser Permanente Colorado, Inst Hlth Res, Denver, CO USA
[3] HealthPartners Inst Educ & Res, Minneapolis, MN USA
[4] Marshfield Clin Res Fdn, Marshfield, WI USA
[5] Weston Ctr, Marshfield Clin, Dept Hematol Oncol, Weston, WI USA
[6] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
[7] Henry Ford Hlth Syst, Dept Publ Hlth Sci, Detroit, MI USA
[8] Kaiser Permanente No Calif, Div Res, Oakland, CA USA
[9] Kaiser Permanente Hawaii, Ctr Hlth Res, Honolulu, HI USA
[10] Essentia Inst Rural Hlth, Duluth, MN USA
关键词
D O I
10.1158/1055-9965.EPI-12-0545
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: In metastatic colorectal cancer (mCRC), mutations in the KRAS gene predict poor response to EGF receptor (EGFR) inhibitors. Clinical treatment guidelines now recommend KRAS testing if EGFR inhibitors are considered. Our study investigates the clinical uptake and utilization of KRAS testing. Methods: We included 1,188 patients with mCRCs diagnosed from 2004 to 2009, from seven integrated health care delivery systems with a combined membership of 5.5 million. We used electronic medical records and targeted manual chart review to capture the complexity and breadth of real-world clinical oncology care. Results: Overall, 428 patients (36%) received KRAS testing during their clinical care, and 266 (22%) were treated with EGFR inhibitors. Age at diagnosis (P = 0.0034), comorbid conditions (P = 0.0316), and survival time from diagnosis (P < 0.0001) influence KRAS testing and EGFR inhibitor prescribing. The proportion who received KRAS testing increased from 7% to 97% for those treated in 2006 and 2010, respectively, and 83% of all treated patients had a KRAS wild-type genotype. Most patients with a KRAS mutation (86%) were not treated with EGFR inhibitors. The interval between mCRC diagnosis and receipt of KRAS testing decreased from 26 months (2006) to 10 months (2009). Conclusions: These findings show rapid uptake and incorporation of this predictive biomarker into clinical oncology care. Impact: In this delivery setting, KRAS testing is widely used to guide treatment decisions with EGFR inhibitors in patients with mCRCs. An important future research goal is to evaluate utilization of KRAS testing in other delivery settings in the United States. Cancer Epidemiol Biomarkers Prey; 22(1); 91-101. (C) 2012 AACR.
引用
收藏
页码:91 / 101
页数:11
相关论文
共 50 条
  • [31] KRAS Mutations and Anti-Epidermal Growth Factor Receptor Therapy in Colorectal Cancer With Lymph Node Metastases REPLY
    Sartore-Bianchi, Andrea
    Artale, Salvatore
    Veronese, Silvio
    Gambacorta, Marcello
    Siena, Salvatore
    JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (01) : 159 - 159
  • [32] Oncogenic fingerprint of epidermal growth factor receptor pathway and emerging epidermal growth factor receptor blockade resistance in colorectal cancer
    Sobani, Zain A.
    Sawant, Ashwin
    Jafri, Mikram
    Correa, Amit Keith
    Sahin, Ibrahim Halil
    WORLD JOURNAL OF CLINICAL ONCOLOGY, 2016, 7 (05): : 340 - 351
  • [33] Prognostic and predictive biomarkers for epidermal growth factor receptor-targeted therapy in colorectal cancer: Beyond KRAS mutations
    Custodio, Ana
    Feliu, Jaime
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2013, 85 (01) : 45 - 81
  • [34] Oncogenic KRAS Desensitizes Colorectal Tumor Cells to Epidermal Growth Factor Receptor Inhibition and Activation
    van Houdt, Winan J.
    Hoogwater, Frederik J. H.
    de Bruijn, Menno T.
    Emmink, Benjamin L.
    Nijkamp, Maarten W.
    Raats, Danielle A. E.
    van der Groep, Petra
    van Diest, Paul
    Rinkes, Inne H. M. Borel
    Kranenburg, Onno
    NEOPLASIA, 2010, 12 (06): : 443 - U23
  • [35] Optimizing administration of epidermal growth factor receptor-targeted agents in the treatment of colorectal cancer
    Van Cutsem, Eric
    CLINICAL COLORECTAL CANCER, 2007, 6 : S60 - S65
  • [36] Targeting the Epidermal Growth Factor Receptor in the Treatment of Colorectal CancerState of the Art
    Robert B. Diasio
    Jeanne Fourie
    Drugs, 2006, 66 : 1441 - 1463
  • [37] Predictive Biomarkers for Anti-Epidermal Growth Factor Receptor Therapy: Beyond KRAS Testing
    Ashraf, Noman
    Kothari, Nishi
    Kim, Richard
    JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2014, 12 (10): : 1433 - 1442
  • [38] Trichomegaly of the eyelashes after lung cancer treatment with the epidermal growth factor receptor inhibitor erlotinib
    Braiteh, Fadi
    Kurzrock, Razelle
    Johnson, Faye M.
    JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (20) : 3460 - 3462
  • [39] EPIDERMAL GROWTH-FACTOR RECEPTOR EXPRESSION IN COLORECTAL-CANCER
    STEELE, RJC
    KELLY, P
    ELLUL, B
    EREMIN, O
    BRITISH JOURNAL OF SURGERY, 1990, 77 (12) : 1352 - 1354
  • [40] Targeting the epidermal growth factor receptor in colorectal cancer: clinical results
    Adenis, A
    Hebbar, M
    BULLETIN DU CANCER, 2005, 92 : S21 - S28