Title | Chemotherapy of osteosarcoma: beyond conventional approaches to future concepts | ||
Authors | Ch. Dokos, Κ. Kalousis, A. Kouyoumtzis and M. Mironidou-Tzouveleki
A’ Laboratory of Pharmacology, Medical School, Aristotle University, Thessaloniki, Greece |
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Citation | Dokos, C., Kalousis, K., Kouyoumtzis, A. and Minoridou-Tzouveleki, M.: Chemotherapy of osteosarcoma: beyond conventional approaches to future concepts, Epitheorese Klin. Farmakol. Farmakokinet. 22(2): 133-137 (2008) | ||
Publication Date | 23-25 May 2008 | ||
Full Text Language | English | ||
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Keywords | Osteosarcoma, chemotherapy, therapeutics, methotrexate, ifosfamide, cisplatin, doxorubicin, bisphosphonates, prognosis, COX-2 inhibitors. | ||
Other Terms | Review article | ||
Summary | Osteosarcoma or osteogenic sarcoma is a frequent primary malignant bone tumor with complex unbalanced karyotypes. It is primarily located in the metaphyseal region of distal femur and presents both numerical and structural cytogenetic abnormalities. It appears mostly in children and adolescents (men) and metastases emerge in more than 30% of the cases from the reactive zone of tumor (nodules called satellites) locally (as skip lesion) or systematically (lungs, other bones). Neoadjuvant multiagent chemotherapy seems to be the first line solution. Methotrexate, ifosfamide, cisplatin and doxorubicin are the main four cytostatic drugs used in chemotherapy protocols for osteosarcoma so as to increase the percentage of healing and further reduce mutilating surgery and toxicity. Even though survival rate has increased to 60% the problem of non-response to chemotherapy protocols still remains. Unfortunately it is estimated that 20% of the patients die from tumor metastasis. Beyond conventional chemotherapy protocols, studies indicate the need for prognostic factors in the chemotherapy response. Additionally new agents are under research for their therapeutic value in both neoadjuvant chemotherapy and chemotherapy resistance. Liposomal doxorubicin, bisphosphonates (zoledronic acid), VEGF inhibiting monoclonal antibodies, COX-2 inhibitors (meloxicam) are few of the future antineoplastic agents for established osteosarcoma therapy. | ||
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