Quantitative HER2 Protein Levels Predict Outcome In Fluorescence In Situ Hybridization-Positive Patients With Metastatic Breast Cancer Treated With Trastuzumab

被引:44
作者
Lipton, Allan [1 ]
Koestler, Wolfgang J. [2 ]
Leitzel, Kim [1 ]
Ali, Suhail M. [1 ,3 ]
Sperinde, Jeff [4 ]
Weidler, Jodi [5 ]
Paquet, Agnes [5 ]
Sherwood, Thomas [5 ]
Huang, Weidong [5 ]
Bates, Michael [5 ]
机构
[1] Penn State Hershey Med Ctr, Div Hematol Oncol, Hershey, PA 17033 USA
[2] Med Univ Vienna, Div Clin Oncol, Dept Med 1, Vienna, Austria
[3] Lebanon Vet Affairs Med Ctr, Lebanon, PA USA
[4] Monogram Biosci, Div Res & Dev, San Francisco, CA USA
[5] Monogram Biosci, Div Clin Res, San Francisco, CA USA
关键词
HER2/neu; erbB2; metastatic breast cancer; trastuzumab; predictive biomarker; fluorescence in situ hybridization; VeraTag; HERmark; immunohistochemistry; ADJUVANT CHEMOTHERAPY; MONOCLONAL-ANTIBODY; EFFICACY; RECOMMENDATIONS; AMPLIFICATION; SURVIVAL; THERAPY; BENEFIT; SAFETY; ASSAY;
D O I
10.1002/cncr.25430
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND: Only a portion of breast cancer patients currently selected for trastuzumab therapy respond. METHODS: Using a novel assay (HERmark) to quantify total human epidermal growth factor receptor 2 (HER2) expression, the authors examined outcomes in 102 trastuzumab-treated metastatic breast cancer patients previously assessed as immunohistochemistry (IHC) 3+ by local but not central IHC, or fluorescence in situ hybridization (FISH) positive, and then retested by central FISH. RESULTS: Of 102 MBC patients previously scored as IHC 3+ or 2+/FISH-positive and treated with trastuzumab-containing regimens, 98 had both central FISH and HER2 total expression values. Sixty-six of 76 central FISH-positive patients (87%) had high HER2 total expression levels (concordant positive), and 19 of 22 central FISH-negative patients (86%) were HER2 total expression low (concordant negative). Fourteen percent (3 of 22) of central FISH-negative patients were HER2 total expression high (discordant HER2 total expression high), and 13% (10 of 76) of central FISH-positive patients were HER2 total expression low (discordant HER2 total expression low). The concordant positive group had a significantly longer time to progression (TTP, median = 11.3 months) compared with the concordant negative group (median TTP, 4.5 months; hazard ratio [HR] = 0.42, P < .001), and also compared with the discordant HER2 total expression low group (median TTP, 3.7 months; HR = 0.43, P = .01). The discordant HER2 total expression low group behaved similarly compared with concordant negatives (HR = 1, P = .99). In analyses restricted to central FISH-positive patients only (n = 77), Cox proportional hazards multivariate regression identified HER2 total expression as an independent predictor of TTP (HR = 0.29, P = .0015) and overall survival (HR = 0.19, P < .001). CONCLUSIONS: A subset of patients with HER2 gene amplification by FISH express low levels of HER2 protein and have reduced response to trastuzumab-containing therapy, similar to FISH-negative patients. This cohort represents a training dataset, and the observed relationships and derived cutoffs require validation in an independent cohort of trastuzumab-treated metastatic breast cancer patients. Cancer 2010;116:5168-78. (c) 2010 American Cancer Society.
引用
收藏
页码:5168 / 5178
页数:11
相关论文
共 24 条
[1]
AMPLIFICATION OF C-ERBB-2 AND AGGRESSIVE HUMAN-BREAST TUMORS [J].
ALI, IU ;
CAMPBELL, G ;
LIDEREAU, R ;
CALLAHAN, R .
SCIENCE, 1988, 240 (4860) :1795-1796
[2]
Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease [J].
Cobleigh, MA ;
Vogel, CL ;
Tripathy, D ;
Robert, NJ ;
Scholl, S ;
Fehrenbacher, L ;
Wolter, JM ;
Paton, V ;
Shak, S ;
Lieberman, G ;
Slamon, DJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2639-2648
[3]
Comparison of HER2 status by fluorescence in situ hybridization and immunohistochemistry to predict benefit from dose escalation of adjuvant doxorubicin-based therapy in node-positive breast cancer patients [J].
Dressler, LG ;
Berry, DA ;
Broadwater, G ;
Cowan, D ;
Cox, K ;
Griffin, S ;
Miller, A ;
Tse, J ;
Novotny, D ;
Persons, DL ;
Barcos, M ;
Henderson, IC ;
Liu, ET ;
Thor, A ;
Budman, D ;
Muss, H ;
Norton, L ;
Hayes, DF .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (19) :4287-4297
[4]
Monitoring of serum Her-2/neu predicts response and progression-free survival to trastuzumab-based treatment in patients with metastatic breast cancer [J].
Köstler, WJ ;
Schwab, B ;
Singer, CF ;
Neumann, R ;
Rücklinger, E ;
Brodowicz, T ;
Tomek, S ;
Niedermayr, M ;
Hejna, M ;
Steger, GG ;
Krainer, M ;
Wiltschke, C ;
Zielinski, CC .
CLINICAL CANCER RESEARCH, 2004, 10 (05) :1618-1624
[5]
LARSON J, PATHOL RES IN PRESS
[6]
Reporting recommendations for tumor marker prognostic studies (REMARK) [J].
McShane, LM ;
Altman, DG ;
Sauerbrei, W ;
Taube, SE ;
Gion, M ;
Clark, GM .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (16) :1180-1184
[7]
HER2 status and benefit from adjuvant trastuzumab in breast cancer [J].
Paik, Soonmyung ;
Kim, Chungyeul ;
Wolmark, Norman .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (13) :1409-1411
[8]
Assessment of methods for tissue-based detection of the HER-2/neu alteration in human breast cancer:: A direct comparison of fluorescence in situ hybridization and immunohistochemistry [J].
Pauletti, G ;
Dandekar, S ;
Rong, HM ;
Ramos, L ;
Pong, HJ ;
Seshadri, R ;
Slamon, DJ .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (21) :3651-3664
[9]
HER2 testing by local, central, and reference laboratories in specimens from the North Central Cancer Treatment Group N9831 intergroup adjuvant trial [J].
Perez, Edith A. ;
Suman, Vera J. ;
Davidson, Nancy E. ;
Martino, Silvana ;
Kaufman, Peter A. ;
Lingle, Wilma L. ;
Flynn, Patrick J. ;
Ingle, James N. ;
Visscher, Daniel ;
Jenkins, Robert B. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (19) :3032-3038
[10]
Trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer [J].
Piccart-Gebhart, MJ ;
Procter, M ;
Leyland-Jones, B ;
Goldhirsch, A ;
Untch, M ;
Smith, I ;
Gianni, L ;
Baselga, J ;
Bell, R ;
Jackisch, C ;
Cameron, D ;
Dowsett, M ;
Barrios, CH ;
Steger, G ;
Huang, CS ;
Andersson, M ;
Inbar, M ;
Lichinitser, M ;
Láng, I ;
Nitz, U ;
Iwata, H ;
Thomssen, C ;
Lohrisch, C ;
Suter, TM ;
Ruschoff, J ;
Süto, T ;
Greatorex, V ;
Ward, C ;
Straehle, C ;
McFadden, E ;
Dolci, MS ;
Gelber, RD .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (16) :1659-1672