Inhibition of receptor tyrosine kinases in combination with chemotherapy for the treatment of breast cancer

被引:4
|
作者
Moulder, S. L. [1 ,2 ]
Craft, B. S. [3 ]
Hortobagyi, G. N. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Unit 1354, Dept Breast Med Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Phase Program 1, Houston, TX 77030 USA
[3] Univ Mississippi, Med Ctr, Div Hematol & Oncol, University, MS 38677 USA
关键词
breast cancer; biotherapy; tyrosine kinase; targeted therapy; lapatinib; trastuzumab; bevacizumab;
D O I
10.2174/187152008784533080
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although significant advances have been made in the treatment of breast cancer using chemotherapy, less than half of the patients treated for localized breast cancer benefit from adjuvant chemotherapy and most patients with metastatic cancer eventually develop disease that is chemotherapy resistant. Targeted agents, such as inhibitors of tyrosine kinases, offer the opportunity to reverse chemotherapy resistance and enhance response in patients with localized and advanced breast cancer. Such combined approaches have been established for the treatment of advanced breast cancer and are now demonstrating benefit in the adjuvant arena. This review summarizes the results of several trials involving the use of tyrosine kinase inhibition in combination with chemotherapy for the treatment of breast cancer and discusses future directions for breast cancer biotherapy.
引用
收藏
页码:481 / 487
页数:7
相关论文
共 50 条
  • [21] Targeting receptor tyrosine kinases in HER2-negative breast cancer
    Anandappa, Gayathri
    Turner, Nicholas C.
    CURRENT OPINION IN ONCOLOGY, 2013, 25 (06) : 594 - 601
  • [22] Different profile of receptor tyrosine kinases expression in breast cancer molecular subtypes
    Babyshkina, N.
    Dronova, T.
    Vtorushin, S.
    Slonimskaya, E.
    Cherdyntseva, N.
    ANNALS OF ONCOLOGY, 2020, 31 : S1224 - S1224
  • [23] Programmed Death-Ligand 1 and Receptor Tyrosine Kinases in Breast Cancer
    Ayoub, Nehad
    Al-Diabat, Muhsen
    Al-Shorman, Moath
    Al-Eitan, Laith
    CANCER RESEARCH, 2024, 84 (09)
  • [24] Expression of activated type I receptor tyrosine kinases in early breast cancer
    Spears, Melanie
    Pederson, Hans Christian
    Lyttle, Nicola
    Gray, Claire
    Quintayo, Mary Anne
    Brogan, Lyndsay
    Thomas, Jeremy St J.
    Kerr, Gillian R.
    Jack, Wilma J. L.
    Kunkler, Ian H.
    Cameron, David A.
    Chetty, Udi
    Bartlett, John M. S.
    BREAST CANCER RESEARCH AND TREATMENT, 2012, 134 (02) : 701 - 708
  • [25] Expression of the HERI-4 family of receptor tyrosine kinases in breast cancer
    Witton, CJ
    Reeves, JR
    Going, JJ
    Cooke, TG
    Bartlett, JMS
    JOURNAL OF PATHOLOGY, 2003, 200 (03): : 290 - 297
  • [26] Receptor tyrosine kinases (RTKs) in breast cancer: signaling, therapeutic implications and challenges
    Butti, Ramesh
    Das, Sumit
    Gunasekaran, Vinoth Prasanna
    Yadav, Amit Singh
    Kumar, Dhiraj
    Kundu, Gopal C.
    MOLECULAR CANCER, 2018, 17
  • [27] Expression of activated type I receptor tyrosine kinases in early breast cancer
    Melanie Spears
    Hans Christian Pederson
    Nicola Lyttle
    Claire Gray
    Mary Anne Quintayo
    Lyndsay Brogan
    Jeremy St. J Thomas
    Gillian R. Kerr
    Wilma J. L. Jack
    Ian H. Kunkler
    David A. Cameron
    Udi Chetty
    John M. S. Bartlett
    Breast Cancer Research and Treatment, 2012, 134 : 701 - 708
  • [28] Receptor tyrosine kinases (RTKs) in breast cancer: signaling, therapeutic implications and challenges
    Ramesh Butti
    Sumit Das
    Vinoth Prasanna Gunasekaran
    Amit Singh Yadav
    Dhiraj Kumar
    Gopal C. Kundu
    Molecular Cancer, 17
  • [29] Inhibition of the epidermal growth factor receptor family of tyrosine kinases as an approach to cancer chemotherapy: Progression from reversible to irreversible inhibitors
    Fry, DW
    PHARMACOLOGY & THERAPEUTICS, 1999, 82 (2-3) : 207 - 218
  • [30] Targeted Inhibition of Multiple Receptor Tyrosine Kinases in Mesothelioma
    Ou, Wen-Bin
    Hubert, Christopher
    Corson, Joseph M.
    Bueno, Raphael
    Flynn, Daniel L.
    Sugarbaker, David J.
    Fletcher, Jonathan A.
    NEOPLASIA, 2011, 13 (01): : 12 - U26