Adjuvant trastuzumab: A milestone in the treatment of HER-2-positive early breast cancer

被引:153
作者
Baselga, Jose
Perez, Edith A.
Pienkowski, Tadeusz
Bell, Richard
机构
[1] Vall Hebron Univ Hosp, Oncol Serv, Barcelona 08035, Spain
[2] Mayo Clin, Jacksonville, FL 32224 USA
[3] Ctr Canc, Breast Canc Dept, Warsaw, Poland
[4] Andrew Love Canc Ctr, Geelong, Vic, Australia
关键词
adjuvant; early breast cancer; trastuzumab; HER-2positive; clinical trial;
D O I
10.1634/theoncologist.11-90001-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Up to one fourth of women diagnosed with early breast cancer (EBC) have tumors that are human epidermal growth factor receptor 2 (HER-2) positive. This is associated with a high risk of relapse and death from metastatic disease. Trastuzumab, a monoclonal antibody directed against the extracellular domain of HER-2, improves survival and quality of life in women with HER-2-positive metastatic breast cancer receiving chemotherapy. Four major adjuvant trials-Herceptin (R) Adjuvant (HERA), National Surgical Adjuvant Breast and Bowel Project (NSABP) B-31, North Central Cancer Treatment Group (NCCTG) N9831, and Breast Cancer International Research Group (BCIRG) 006-including between them > 13,000 women with HER-2-positive EBC, have investigated different adjuvant treatment approaches with trastuzumab. These trials have shown that trastuzumab reduces the 3-year risk of recurrence by about half in this population. The benefit was similar across the trials despite differences in patient populations, chemotherapy regimens, and sequencing of treatment. At a 2-year follow-up, interim results from the combined analysis of the NSABP B-31 and NCCTG N9831 trials showed a one third lower mortality for trastuzumab, and there was a trend toward an overall survival benefit in the HERA and BCIRG trials. A small Finnish trial, FinHer, investigating another regimen of trastuzumab, has also shown similarly positive results. Further follow-up of the major adjuvant trials will clarify the survival benefit for women receiving trastuzumab, as well as the optimal treatment duration (1 or 2 years). Notably, cardiac events in the trastuzumab-containing arms of these trials have remained within acceptable levels, with a slightly higher (0.6%-3.3%) incidence of congestive heart failure that mostly responded to treatment. Further follow-up will provide information on long-term cardiac safety. Overall, results from clinical trials are sufficiently compelling to consider 1 year of adjuvant trastuzumab treatment for women with HER-2-positive EBC based on the risk:benefit ratio demonstrated in these studies.
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页码:4 / 12
页数:9
相关论文
共 15 条
[1]   Phase II study of efficacy, safety, and pharmacokinetics of trastuzumab monotherapy administered on a 3-weekly schedule [J].
Baselga, J ;
Carbonell, X ;
Castañeda-Soto, NJ ;
Clemens, M ;
Green, M ;
Harvey, V ;
Morales, S ;
Barton, C ;
Ghahramani, P .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (10) :2162-2171
[2]   Adjuvant docetaxel or vinorelbine with or without trastuzumab for breast cancer [J].
Joensuu, H ;
Kellokumpu-Lehtinen, P ;
Bono, P ;
Alanko, T ;
Kataja, V ;
Asola, R ;
Utriainen, T ;
Kokko, R ;
Hemminki, A ;
Tarkkanen, M ;
Turpeenniemi-Hujanen, T ;
Jyrkkiö, S ;
Flander, M ;
Helle, L ;
Ingalsuo, S ;
Johansson, K ;
Jääskeläinen, A ;
Pajunen, M ;
Rauhala, M ;
Kaleva-Kerola, J ;
Salminen, T ;
Leinonen, M ;
Elomaa, I ;
Isola, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (08) :809-820
[3]   Randomized phase II trial of the efficacy and safety of trastuzumab combined with docetaxel in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer administered as first-line treatment:: The M77001 study group [J].
Marty, M ;
Cognetti, F ;
Maraninchi, D ;
Snyder, R ;
Mauriac, L ;
Tubiana-Hulin, M ;
Chan, S ;
Grimes, D ;
Antón, A ;
Lluch, A ;
Kennedy, J ;
O'Byrne, K ;
Conte, P ;
Green, M ;
Ward, C ;
Mayne, K ;
Extra, JM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (19) :4265-4274
[4]   Effects on quality of life of combined trastuzumab and chemotherapy in women with metastatic breast cancer [J].
Osoba, D ;
Slamon, DJ ;
Burchmore, M ;
Murphy, M .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (14) :3106-3113
[5]  
Perez EA, 2005, J CLIN ONCOL, V23, p17S
[6]  
Perez EA, 2005, 41 AM SOC CLIN ONC A
[7]   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
[8]   HER2 and responsiveness of breast cancer to adjuvant chemotherapy [J].
Pritchard, KI ;
Shepherd, LE ;
O'Malley, FP ;
Andrulis, IL ;
Tu, DS ;
Bramwell, VH ;
Levine, MN .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (20) :2103-2111
[9]   Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer [J].
Romond, EH ;
Perez, EA ;
Bryant, J ;
Suman, VJ ;
Geyer, CE ;
Davidson, NE ;
Tan-Chiu, E ;
Martino, S ;
Paik, S ;
Kaufman, PA ;
Swain, SM ;
Pisansky, TM ;
Fehrenbacher, L ;
Kutteh, LA ;
Vogel, VG ;
Visscher, DW ;
Yothers, G ;
Jenkins, RB ;
Brown, AM ;
Dakhil, SR ;
Mamounas, EP ;
Lingle, WL ;
Klein, PM ;
Ingle, JN ;
Wolmark, N .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (16) :1673-1684
[10]  
Slamon D, 2005, BREAST CANCER RES TR, V94, pS5