EGFR FISH assay predicts for response to cetuximab in chemotherapy refractory colorectal cancer patients

被引:213
作者
Cappuzzo, F. [1 ]
Finocchiaro, G. [1 ,2 ]
Rossi, E. [3 ]
Jaenne, P. A. [4 ]
Carnaghi, C. [5 ]
Calandri, C. [6 ]
Bencardino, K. [7 ]
Ligorio, C.
Ciardiello, F. [7 ]
Pressiani, T. [1 ]
Destro, A. [1 ,8 ]
Roncalli, M. [1 ,8 ]
Crino, L. [9 ]
Franklin, W. A. [2 ]
Santoro, A. [1 ]
Varella-Garcia, M. [1 ]
机构
[1] Ist Clin Humanitas IRCCS, Dept Med Oncol, Rozzano, Italy
[2] Univ Colorado, Ctr Canc, Dept Med Med Oncol, Aurora, CO USA
[3] CINECA Interuniv Consortium, Bologna, Italy
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[5] Bellaria Maggiore Hosp, Dept Med Oncol, Bologna, Italy
[6] San Matteo Hosp, Dept Med Oncol, Pavia, Italy
[7] Univ Naples 2, Dept Med Oncol, Naples, Italy
[8] Univ Milan, Ist Clin Humanitas IRCCS, Pathol Unit, Rozzano, Italy
[9] Osped Silvestrini, Dept Med Oncol, Perugia, Italy
关键词
cetuximab; colon cancer; EGFR; fluorescence in situ hybridization;
D O I
10.1093/annonc/mdm492
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Standardized conditions to distinguish subpopulations of colorectal cancer (CRC) patients more and less sensitive to cetuximab therapy remain undefined. Materials and methods: We retrospectively analyzed epidermal growth factor receptor (EGFR) copy number by fluorescence in situ hybridization (FISH) in paraffin-embedded tumor blocks from 85 chemorefractory CRC patients treated with cetuximab. Results were analyzed according to different score systems previously reported in colorectal and lung cancers. The primary end point of the study was identification of the EGFR FISH score that best associates with response rate (RR). Results: Using receiver operating characteristic (ROC) analysis, the cut-off that best discriminated responders versus nonresponders to cetuximab was a mean of 2.92 EGFR gene copies per cell. This model showed sensitivity of 58.6% (95% confidence interval (CI) = 47.1-70.1) and specificity of 93.3% (95% CI = 80.6-100). EGFR FISH-positive patients (N = 43, 50.6%) had significantly higher RR (P = 0.0001) and significantly longer time to disease progression (P = 0.02) than EGFR FISH negative (N = 42, 49.4%). Other scoring systems resulted less accurate in discriminating patients with the highest likelihood of response to cetuximab therapy. Conclusions: CRC patients with high EGFR gene copy number have an increased likelihood to respond to cetuximab therapy. Prospective clinical trials with a careful standardization of assay conditions and pattern interpretation are urgently needed.
引用
收藏
页码:717 / 723
页数:7
相关论文
共 36 条
  • [21] KRAS mutation is an important predictor of resistance to therapy with epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer
    Massarelli, Erminia
    Varella-Garcia, Marileila
    Tang, Ximing
    Xavier, Ana C.
    Ozburn, Natalie C.
    Liu, Diane D.
    Bekele, Benjamin N.
    Herbst, Roy S.
    Wistuba, Ignacio I.
    [J]. CLINICAL CANCER RESEARCH, 2007, 13 (10) : 2890 - 2896
  • [22] Evaluation of the epidermal growth factor receptor (EGFR) in colorectal tumours and lymph node metastases
    McKay, JA
    Murray, LJ
    Curran, S
    Ross, VG
    Clark, C
    Murray, GI
    Cassidy, J
    McLeod, HL
    [J]. EUROPEAN JOURNAL OF CANCER, 2002, 38 (17) : 2258 - 2264
  • [23] Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: A phase III trial of the National Cancer Institute of Canada clinical trials group
    Moore, Malcolm J.
    Goldstein, David
    Hamm, John
    Figer, Arie
    Hecht, Joel R.
    Gallinger, Steven
    Au, Heather J.
    Murawa, Pawel
    Walde, David
    Wolff, Robert A.
    Campos, Daniel
    Lim, Robert
    Ding, Keyue
    Clark, Gary
    Voskoglou-Nomikos, Theodora
    Ptasynski, Mieke
    Parulekar, Wendy
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (15) : 1960 - 1966
  • [24] Gene copy number for epidermal growth factor receptor (EGFR) and clinical response to antiEGFR treatment in colorectal cancer: a cohort study
    Moroni, M
    Veronese, S
    Benvenuti, S
    Marrapese, G
    Sartore-Bianchi, A
    Di Nicolantonio, F
    Gambacorta, M
    Siena, S
    Bardelli, A
    [J]. LANCET ONCOLOGY, 2005, 6 (05) : 279 - 286
  • [25] Differential effects of gefitinib and cetuximab on non-small-cell lung cancers bearing epidermal growth factor receptor mutations
    Mukohara, T
    Engelman, JA
    Hanna, NH
    Yeap, BY
    Kobayashi, S
    Lindeman, N
    Halmos, B
    Pearlberg, J
    Tsuchihashi, Z
    Cantley, LC
    Tenen, DG
    Johnson, BE
    Jänne, PA
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (16): : 1185 - 1194
  • [26] EGFR mutations in lung cancer:: Correlation with clinical response to gefitinib therapy
    Paez, JG
    Jänne, PA
    Lee, JC
    Tracy, S
    Greulich, H
    Gabriel, S
    Herman, P
    Kaye, FJ
    Lindeman, N
    Boggon, TJ
    Naoki, K
    Sasaki, H
    Fujii, Y
    Eck, MJ
    Sellers, WR
    Johnson, BE
    Meyerson, M
    [J]. SCIENCE, 2004, 304 (5676) : 1497 - 1500
  • [27] KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib
    Pao, W
    Wang, TY
    Riely, GJ
    Miller, VA
    Pan, QL
    Ladanyi, M
    Zakowski, MF
    Heelan, RT
    Kris, MG
    Varmus, HE
    [J]. PLOS MEDICINE, 2005, 2 (01) : 57 - 61
  • [28] Epidermal growth factor receptor (EGFR) antibody down-regulates mutant receptors and inhibits tumors expressing EGFR mutations
    Perez-Torres, Marianela
    Guix, Marta
    Gonzalez, Adriana
    Arteaga, Carlos L.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (52) : 40183 - 40192
  • [29] Epidermal growth factor receptor gene copy number and clinical outcome of metastatic colorectal cancer treated with panitumumab
    Sartore-Bianchi, Andrea
    Moroni, Mauro
    Veronese, Silvio
    Carnaghi, Carlo
    Bajetta, Emilio
    Luppi, Gabriele
    Sobrero, Alberto
    Barone, Carlo
    Cascinu, Stefano
    Colucci, Giuseppe
    Cortesi, Enrico
    Nichelatti, Michele
    Gambacorta, Marcello
    Siena, Salvatore
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (22) : 3238 - 3245
  • [30] Epidermal growth factor receptor (EGFR) status in primary colorectal tumors does not correlate with EGFR expression in related metastatic sites: Implications for treatment with EGFR-targeted monoclonal antibodies
    Scartozzi, M
    Bearzi, I
    Berardi, R
    Mandolesi, A
    Fabris, G
    Cascinu, S
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (23) : 4772 - 4778