HER-2 testing and trastuzurnab therapy for metastatic breast cancer: A cost-effectiveness analysis

被引:179
作者
Elkin, EB
Weinstein, KC
Winer, EP
Kuntz, KM
Schnitt, SJ
Weeks, JC
机构
[1] Harvard Univ, Ctr Risk Anal, Cambridge, MA 02138 USA
[2] Sch Publ Hlth, Cambridge, England
[3] Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
[4] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
关键词
D O I
10.1200/JCO.2004.04.158
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Trastuzumab therapy has been shown to benefit metastatic breast cancer patients whose tumors exhibit HER-2 protein overexpression or gene amplification. Several tests of varying accuracy and cost are available to identify candidates for trastuzumab. We estimated the cost-effectiveness of alternative HER-2 testing and trastuzumab treatment strategies. Patients and Methods We performed a decision analysis using a state-transition model to simulate clinical practice in a hypothetical cohort of 65-year-old metastatic breast cancer patients. Outcomes were quality-adjusted life-years (QALYs), lifetime cost, and incremental cost-effectiveness ratio (ICER). Interventions included testing with the HercepTest (DAKO, Carpinteria, CA) immunolhistochemical assay alone, fluorescence in situ hybridization (FISH) alone, and both tests, followed by trastuzumab and chemotherapy for patients with positive test results and chemotherapy alone for patients with negative test results. Results In the base case, initial HercepTest with FISH confirmation of all positive results had an ICER of $125,000 per QALY gained. The incremental cost-effectiveness of initial FISH was $145,000 per QALY gained. Other strategies yielded the same or poorer effectiveness at a higher cost, or lower effectiveness at a lower cost, but with a less favorable ICER. These findings persisted under a range of assumptions, and only changes in test characteristics substantially altered results. Conclusion It is more cost-effective to use FISH alone or as confirmation of all positive HercepTest results, rather than using FISH to confirm only weakly positive results or using HercepTest alone. When multiple tests are available to identify treatment candidates, test characteristics may have a substantial impact on the aggregate costs and effectiveness of treatment. (C) 2004 by American Society of Clinical Oncology.
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页码:854 / 863
页数:10
相关论文
共 93 条
[71]   The HER-2/neu oncogene:: prognostic factor, predictive factor and target for therapy [J].
Ross, JS ;
Fletcher, JA .
SEMINARS IN CANCER BIOLOGY, 1999, 9 (02) :125-138
[72]   Weekly trastuzumab and paclitaxel therapy for metastatic breast cancer with analysis of efficacy by HER2 immunophenotype and gene amplification [J].
Seidman, AD ;
Fornier, MN ;
Esteva, FJ ;
Tan, L ;
Kaptain, S ;
Bach, A ;
Panageas, KS ;
Arroyo, C ;
Valero, V ;
Currie, V ;
Gilewski, T ;
Theodoulou, M ;
Moynahan, ME ;
Moasser, M ;
Sklarin, N ;
Dickler, M ;
D'Andrea, G ;
Cristofanilli, M ;
Rivera, E ;
Hortobagyi, GN ;
Norton, L ;
Hudis, CA .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (10) :2587-2595
[73]   Patterns of HER-2/neu amplification and overexpression in primary and metastatic breast cancer [J].
Simon, R ;
Nocito, A ;
Hübscher, T ;
Bucher, C ;
Torhorst, J ;
Schraml, P ;
Bubendorf, L ;
Mihatsch, MM ;
Moch, H ;
Wilber, K ;
Schötzau, A ;
Kononen, J ;
Sauter, G .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (15) :1141-1146
[74]   STUDIES OF THE HER-2/NEU PROTO-ONCOGENE IN HUMAN-BREAST AND OVARIAN-CANCER [J].
SLAMON, DJ ;
GODOLPHIN, W ;
JONES, LA ;
HOLT, JA ;
WONG, SG ;
KEITH, DE ;
LEVIN, WJ ;
STUART, SG ;
UDOVE, J ;
ULLRICH, A ;
PRESS, MF .
SCIENCE, 1989, 244 (4905) :707-712
[75]   Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. [J].
Slamon, DJ ;
Leyland-Jones, B ;
Shak, S ;
Fuchs, H ;
Paton, V ;
Bajamonde, A ;
Fleming, T ;
Eiermann, W ;
Wolter, J ;
Pegram, M ;
Baselga, J ;
Norton, L .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (11) :783-792
[76]   HUMAN-BREAST CANCER - CORRELATION OF RELAPSE AND SURVIVAL WITH AMPLIFICATION OF THE HER-2 NEU ONCOGENE [J].
SLAMON, DJ ;
CLARK, GM ;
WONG, SG ;
LEVIN, WJ ;
ULLRICH, A ;
MCGUIRE, WL .
SCIENCE, 1987, 235 (4785) :177-182
[77]   THE EFFICACY AND COST-EFFECTIVENESS OF ADJUVANT THERAPY OF EARLY BREAST-CANCER IN PREMENOPAUSAL WOMEN [J].
SMITH, TJ ;
HILLNER, BE .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (04) :771-776
[78]   Chromogenic in situ hybridization -: A practical alternative for fluorescence in situ hybridization to detect HER-2/neu oncogene amplification in archival breast cancer samples [J].
Tanner, M ;
Gancberg, D ;
Di Leo, A ;
Larsimont, D ;
Rouas, G ;
Piccart, MJ ;
Isola, J .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (05) :1467-1472
[79]   HER-2/neu in breast cancer:: Interobserver variability and performance of immunohistochemistry with 4 antibodies compared with fluorescent in situ hybridization [J].
Thomson, TA ;
Hayes, MM ;
Spinelli, JJ ;
Hilland, E ;
Sawrenko, C ;
Phillips, D ;
Dupuis, B ;
Parker, RL .
MODERN PATHOLOGY, 2001, 14 (11) :1079-1086
[80]  
Tsuda H, 2001, CANCER-AM CANCER SOC, V92, P2965, DOI 10.1002/1097-0142(20011215)92:12<2965::AID-CNCR10156>3.0.CO