Onkologie. 2014:8(5):231-233

Targeted therapy versus conventional cytostatics

Roman Goněc1,2, ©árka Kozáková1
1 Ústavní lékárna, Masarykův onkologický ústav, Brno
2 Farmaceutická fakulta, Veterinární a farmaceutická univerzita v Brně

Targeted therapy represents leading branch of oncological research. Understanding of molecular phenomena that stand behind cancer

processes enables us to use drugs that are targeted against these processes. Either monoclonal antibodies, e.g. protein molecules, or

small drugs, i.e. smaller chemical entities are involved. In both cases, the target is protein molecule exprimed by tumour cell. Conventional

cytostatics play still major role in the therapy of oncological diseases. This is based on much experience with their use as well as the

fact that for some diagnoses there have not been any targeted drugs available yet. The properties of both groups are united in conjugated

molecules, where toxic conventional cytostatic thanks to the bond with a monoclonal antibody or small drug can be transported

directly to the tumour cell within the body.

Keywords: targeted therapy, cytostatics, monoclonal antibody, small drug, conjugated molecule

Published: October 16, 2014  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Goněc R, Kozáková ©. Targeted therapy versus conventional cytostatics. Onkologie. 2014;8(5):231-233.
Download citation

References

  1. Tomáąek J, Berkovcová J. Onkogeny RAS - prediktivní molekulární marker u kolorektálního karcinomu. Klin onkol 2013; 26(5): 366-367.
  2. Noens L, van Lierde MA, et al. Prevalence, determinants, and outcomes of nonadherence to imatinib therapy in patients with chronic myeloid leukemia: the ADAGIO study. Blood. 2009; 113: 5401-5411. Go to original source... Go to PubMed...
  3. De Both A, Kruse V, et al. Compliance with sunitinib treatment in patients with renal cell cancer. ESMO 2012. Abstract 1349. Go to original source...
  4. Zhou CC, et al. Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study. Lancet Oncol. 12, 735-742 (2011). Go to original source... Go to PubMed...
  5. Fiala O, Peąek M, et al. Mutace genu EGFR u pacientů s pokročilým NSCLC. Klin Onkol 2012; 25(4): 267-273. Go to PubMed...
  6. Bailey DG, Dresser G, Arnold JMO. Grapefruit-medication interactions: Forbidden fruit or avoidable consequences? CMAJ 2012. DOI: 10.1503/cmaj.120951. Go to original source... Go to PubMed...
  7. Hasinoff BB. The cardiotoxicity and myocyte damage caused by small molecule anticancer tyrosine kinase inhibitors is correlated with lack of target specificity. Toxicol Appl Pharmacol 2010; 244: 190-195. Go to original source... Go to PubMed...
  8. Jones AL, Barlow M, et al. Management of cardiac health in trastuzumab-treated patients with breast cancer: Updated United Kingdom National Cancer Research Institute recommendations for monitoring. Br J Cancer 2009. 100: 684-692. Go to original source... Go to PubMed...
  9. Parul Singh, Abhishek Singh. Ocular adverse effects of anti-cancer chemotherapy and targeted therapy. Journal of Cancer Therapeutics & Research 2012, http://www.hoajonline.com/journals/pdf/2049-7962-1-5.pdf. Go to original source...
  10. Watters AL, Epstein JB, Agulnik M. Oral complications of targeted cancer therapies: A narrative literature review. Oral Oncology 47 2011: 441-448. Go to original source... Go to PubMed...
  11. Chabner BA, Roberts TG Jr. Timeline: Chemotherapy and the war on cancer. Nat Rev Cancer 2005; 5: 67-72. Go to original source... Go to PubMed...
  12. Sedláková I, Laco J, et al. Proteiny rezistence a chemorezistence u pacientek s karcinomem ovaria. Klin Onkol 2012; 25(6): 457-463. Go to PubMed...
  13. Jain RK. Transport of molecules in the tumor interstitium: a review. Cancer Res 1987; 47: 3039-3051.
  14. Zinzani PL, Viviani S, et al. Brentuximab vedotin in relapsed/refraktory Hodgkin's lymphoma: Italian experience and results od the use in the daily clinic outside clinical trials. Haematologica. 2013;98:xxx. Pre-published online. Doi: 10.3324/ haematol.2012.083048. Go to original source... Go to PubMed...
  15. Pro B, Advani R, et al. Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol. 2012; 30(18): 2190-2196. Go to original source... Go to PubMed...
  16. Burris HIII, Rugo H, et al. Phase II study of the antibody-drug conjugate trastuzumab-DM1 for the treatment of human epidermal growth factor receptor 2 (HER2)-positive breast cancer after prior HER2-directed therapy. J Clin Oncol 2011; 29: 398-405. Go to original source... Go to PubMed...
  17. Krop IE, LoRusso P, et al. A phase II study of trastuzumab emtansine in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer who were previously treated with trastuzumab, lapatinib, an anthracycline, a taxane and capecitabine. J Clin Oncol 2012; 30: 3234-3241. Go to original source... Go to PubMed...
  18. Lewis Phillips GD, Fields CT, et al. Dual Targeting of HER2-Positive Cancer with Trastuzumab Emtansine and Pertuzumab: Critical Role for Neuregulin Blockade in Antitumor Response to Combination Therapy. Clin Cancer Res 2014; 20: 456-468. Go to original source... Go to PubMed...
  19. Dosio F, Milla P, Cattel L. EC-145, a folate-targeted Vinca alkaloid conjugate for the potential treatment of folate receptor-expressing cancers. Curr Opin Investig Drugs. 2010 Dec; 11(12): 1424-1433. Go to PubMed...




Oncology

Madam, Sir,
please be aware that the website on which you intend to enter, not the general public because it contains technical information about medicines, including advertisements relating to medicinal products. This information and communication professionals are solely under §2 of the Act n.40/1995 Coll. Is active persons authorized to prescribe or supply (hereinafter expert).
Take note that if you are not an expert, you run the risk of danger to their health or the health of other persons, if you the obtained information improperly understood or interpreted, and especially advertising which may be part of this site, or whether you used it for self-diagnosis or medical treatment, whether in relation to each other in person or in relation to others.

I declare:

  1. that I have met the above instruction
  2. I'm an expert within the meaning of the Act n.40/1995 Coll. the regulation of advertising, as amended, and I am aware of the risks that would be a person other than the expert input to these sites exhibited


No

Yes

If your statement is not true, please be aware
that brings the risk of danger to their health or the health of others.