Standards in adjuvant systemic therapy of breast cancer

被引:0
作者
Reinisch, Dr. M. [1 ]
Kuemmel, S. [1 ]
机构
[1] Kliniken Essen Mitte, Senol Interdisziplinares Brustzentrum, D-45136 Essen, Germany
来源
ONKOLOGE | 2015年 / 21卷 / 11期
关键词
Breast cancer; Adjuvant chemotherapy; Targeted therapy; Antineoplastic agents; hormonal; Rare subgroups; CHEMOTHERAPY REGIMENS; PHASE-II; TRIAL; WOMEN; TRASTUZUMAB; PERTUZUMAB; RISK; CYCLOPHOSPHAMIDE; FLUOROURACIL; EPIRUBICIN;
D O I
10.1007/s00761-015-3035-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Survival is the primary goal of adjuvant chemotherapy by curative treatment of potential micrometastases. The standard of care is a chemotherapy regimen containing anthracyclines (epirubicin and doxorubicin) and taxanes (paclitaxel and docetaxel). Possible side effects (e.g. nausea and vomiting, myelosuppression and alopecia), such as cardiotoxicity and secondary leukemia with anthracyclines, polyneuropathy for paclitaxel and hemotoxicity for docetaxel need to be discussed. The use of targeted therapies for breast cancer is steadily increasing. Trastuzumab, an inhibitor of the human epidermal growth factor receptor 2 (Her2) has been the standard medication for Her2 positive breast cancer since 2005. The dual Her2 block with pertuzumab in the neoadjuvant setting is currently used to enlarge the range of anti-Her2 targeted agents and was approved in July 2015. A wide range of antibodies influencing the cell cycle or inhibiting cell metabolism are currently under investigation in clinical studies, e.g. cyclin-dependent kinases 4 and 6 (CDK 4/6) inhibitors, poly(ADP ribose) phosphorylase 1 (PARP) inhibitors and phosphoinositide-3 kinase (PIK) inhibitors. Current therapies focus on tumor biology rather than on the tumor size alone. The therapy of subgroups with breast cancer, such as pregnant, fragile and male patients still represents a special challenge.
引用
收藏
页码:1085 / 1094
页数:10
相关论文
共 44 条
  • [1] Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
  • [2] Comparisons between different polychemotherapy regimens for early breast cancer: meta-analyses of long-term outcome among 100 000 women in 123 randomised trials
    Albain, K.
    Anderson, S.
    Arriagada, R.
    Barlow, W.
    Bergh, J.
    Bliss, J.
    Buyse, M.
    Cameron, D.
    Carrasco, E.
    Clarke, M.
    Correa, C.
    Coates, A.
    Collins, R.
    Costantino, J.
    Cutter, D.
    Cuzick, J.
    Darby, S.
    Davidson, N.
    Davies, C.
    Davies, K.
    Delmestri, A.
    Di Leo, A.
    Dowsett, M.
    Elphinstone, P.
    Evans, V.
    Ewertz, M.
    Gelber, R.
    Gettins, L.
    Geyer, C.
    Goldhirsch, A.
    Godwin, J.
    Gray, R.
    Gregory, C.
    Hayes, D.
    Hill, C.
    Ingle, J.
    Jakesz, R.
    James, S.
    Kaufmann, M.
    Kerr, A.
    MacKinnon, E.
    McGale, P.
    McHugh, T.
    Norton, L.
    Ohashi, Y.
    Paik, S.
    Pan, H. C.
    Perez, E.
    Peto, R.
    Piccart, M.
    [J]. LANCET, 2012, 379 (9814) : 432 - 444
  • [3] Prognosis of Women With Primary Breast Cancer Diagnosed During Pregnancy: Results From an International Collaborative Study
    Amant, Frederic
    von Minckwitz, Gunter
    Han, Sileny N.
    Bontenbal, Marijke
    Ring, Alistair E.
    Giermek, Jerzy
    Wildiers, Hans
    Fehm, Tanja
    Linn, Sabine C.
    Schlehe, Bettina
    Neven, Patrick
    Westenend, Pieter J.
    Mueller, Volkmar
    Van Calsteren, Kristel
    Rack, Brigitte
    Nekljudova, Valentina
    Harbeck, Nadia
    Untch, Michael
    Witteveen, Petronella O.
    Schwedler, Kathrin
    Thomssen, Christoph
    Van Calster, Ben
    Loibl, Sibylle
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (20) : 2532 - +
  • [4] Breast cancer in pregnancy
    Amant, Frederic
    Loibl, Sibylle
    Neven, Patrick
    Van Calsteren, Kristel
    [J]. LANCET, 2012, 379 (9815) : 570 - 579
  • [5] [Anonymous], SAN ANT BREAST CANC
  • [6] [Anonymous], J CLIN ONCOL S
  • [7] Arbeitsgemeinschaft Gynakologische Onkologie e. V. (AGO), 2015, ADJ END THER PRA UND
  • [8] Tailored fluorouracil, epirubicin, and cyclophosphamide compared with marrow-supported high-dose chemotherapy as adjuvant treatment for high-risk breast cancer:: a randomised trial
    Bergh, J
    Wiklund, T
    Erikstein, B
    Lidbrink, E
    Lindman, H
    Malmström, P
    Kellokumpu-Lehtinen, P
    Bengtsson, NO
    Söderlund, G
    Anker, G
    Wist, E
    Ottosson, S
    Salminen, E
    Ljungman, P
    Holte, H
    Nilsson, J
    Blomqvist, C
    Wilking, N
    [J]. LANCET, 2000, 356 (9239) : 1384 - 1391
  • [9] SWOG S0221: A Phase III Trial Comparing Chemotherapy Schedules in High-Risk Early-Stage Breast Cancer
    Budd, George T.
    Barlow, William E.
    Moore, Halle C. F.
    Hobday, Timothy J.
    Stewart, James A.
    Isaacs, Claudine
    Salim, Muhammad
    Cho, Jonathan K.
    Rinn, Kristine J.
    Albain, Kathy S.
    Chew, Helen K.
    Burton, Gary V.
    Moore, Timothy D.
    Srkalovic, Gordan
    McGregor, Bradley A.
    Flaherty, Lawrence E.
    Livingston, Robert B.
    Lew, Danika L.
    Gralow, Julie R.
    Hortobagyi, Gabriel N.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (01) : 58 - U95
  • [10] Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: First report of intergroup trial C9741/cancer and leukemia group B trial 9741
    Citron, ML
    Berry, DA
    Cirrincione, C
    Hudis, C
    Winer, EP
    Gradishar, WJ
    Davidson, NE
    Martino, S
    Livingston, R
    Ingle, JN
    Perez, EA
    Carpenter, J
    Hurd, D
    Holland, JF
    Smith, BL
    Sartor, CI
    Leung, EH
    Abrams, J
    Schilsky, RL
    Muss, HB
    Norton, L
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) : 1431 - 1439