Two drugs are better than one. A short history of combined therapy of ovarian cancer

被引:27
作者
Bukowska, Barbara [1 ]
Gajek, Arkadiusz [1 ]
Marczak, Agnieszka [1 ]
机构
[1] Univ Lodz, Fac Biol & Environm Protect, Inst Biophys, Dept Thermobiol, Pomorska 141-143, PL-90236 Lodz, Poland
来源
WSPOLCZESNA ONKOLOGIA-CONTEMPORARY ONCOLOGY | 2015年 / 19卷 / 05期
关键词
combined therapy; ovarian cancer; synergism; isobolographic analysis;
D O I
10.5114/wo.2014.43975
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Combined therapy of ovarian cancer has a long history. It has been applied for many years. The first drug which was commonly combined with other chemotherapeutics was cisplatin. It turned out to be effective given together with alkylating agents as well as with taxanes. Another drug which is often the basis of first-line therapy is doxorubicin. The use of traditional chemotherapy is often limited due to side effects. This is why new drugs, targeted specifically at cancer cells (e.g. monoclonal antibodies or epidermal growth factor receptor inhibitors), offer a welcome addition when used in combination with conventional anticancer agents. Drugs applied in combination should be synergistic or at least additive. To evaluate the type of interaction between drugs in a plausible sequence, isobolographic analysis is used. This method allows one to assess whether the two agents could make an efficient combination, which might improve the therapy of ovarian cancer.
引用
收藏
页码:350 / 353
页数:4
相关论文
共 29 条
  • [1] Evidence that activation of nuclear factor-κB is essential for the cytotoxic effects of doxorubicin and its analogues
    Ashikawa, K
    Shishodia, S
    Fokt, L
    Priebe, W
    Aggarwal, BB
    [J]. BIOCHEMICAL PHARMACOLOGY, 2004, 67 (02) : 353 - 364
  • [2] Bodnar L., 2004, CONT ONCOL, V8, P435
  • [3] The 4′-O-benzylated doxorubicin analog WP744 overcomes resistance mediated by P-glycoprotein, multidrug resistance protein and breast cancer resistance protein in cell lines and acute myeloid leukemia cells
    Brooks, Tracy A.
    O'Loughlin, Kieran L.
    Minderman, Hans
    Bundy, Brian N.
    Ford, Laurie A.
    Vredenburg, Michael R.
    Bernacki, Ralph J.
    Priebe, Waldemar
    Baer, Maria R.
    [J]. INVESTIGATIONAL NEW DRUGS, 2007, 25 (02) : 115 - 122
  • [4] Structure-based design fill of a new bisintercalating anthracycline antibiotic
    Chaires, JB
    Leng, FF
    Przewloka, T
    Fokt, I
    Ling, YH
    PerezSoler, R
    Priebe, W
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (03) : 261 - 266
  • [5] Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies
    Chou, Ting-Chao
    [J]. PHARMACOLOGICAL REVIEWS, 2006, 58 (03) : 621 - 681
  • [6] The induction of apoptosis by daunorubicin and idarubicin in human trisomic and diabetic fibroblasts
    Dragojew, Sylwia
    Marczak, Agnieszka
    Maszewski, Janusz
    Ilnicki, Krzysztof
    Jozwiak, Zofia
    [J]. CELLULAR & MOLECULAR BIOLOGY LETTERS, 2008, 13 (02) : 182 - 194
  • [7] A randomized clinical trial of cisplatin/paclitaxel versus carboplatin/paclitaxel as first-line treatment of ovarian cancer
    du Bois, A
    Lück, HJ
    Meier, W
    Adams, HP
    Möbus, V
    Costa, S
    Bauknecht, T
    Richter, B
    Warm, M
    Schröder, W
    Olbricht, S
    Nitz, U
    Jackisch, C
    Emons, G
    Wagner, U
    Kuhn, W
    Pfisterer, J
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (17): : 1320 - 1330
  • [8] Isobolographic analysis of interactions: An update on applications and utility
    Gessner, PK
    [J]. TOXICOLOGY, 1995, 105 (2-3) : 161 - 179
  • [9] New findings in the study on the intercalation of bisdaunorubicin and its monomeric analogues with naked and nucleus DNA
    Haj, HTB
    Salerno, M
    Priebe, W
    Kozlowski, H
    Garnier-Suillerot, A
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 2003, 145 (03) : 349 - 358
  • [10] Izycki D, 2004, WSPOLCZESNA ONKOL, V8, P124