Avtor/Urednik     Takač, Iztok
Naslov     Research work at the Department of gynecologic and breast oncology of Maribor teaching hospital
Tip     članek
Vir     In: Takač I, editor. Proceedings of the exchange programme of trainees in obstetrics and gynaecology at Maribor teaching hospital; 2004 Nov 22-25; Maribor. Maribor: Splošna bolnišnica Maribor,
Leto izdaje     2004
Obseg     str. 63-76
Jezik     eng
Abstrakt     A comprehensive research work has been established at the Department of Gynecologic and Breast Oncology of Maribor Teaching Hospital. Among the most important recently conducted studies are a multinational study in patients with ovarian carcinoma using the HMFG1 antibody labeled with 90Yttrium (R1549), (study code: SMART), a multi-national randomized Phase 111 GCIG Intergroup Study comparing 1st line chemotherapy with Gemcitabine, Paclitaxel and Carboplatin versus Paclitaxel and Carboplatin in previously untreated patients with epithelia( ovarian cancer FIGO stages I - IV (study code OVAR-9), a multicenter phase III randomized trial comparing docetaxel in combination with doxorubicin and cyclophosphamide (TAC) versus doxorubicin and cyclophosphamide followed by docetaxel (AC-->T) as adjuvant treatment of operable breast cancer Her2neu negative patients with positive axillary lymph nodes (study code BCIRG 005) and a multicenter phase 111 randomized trial comparing doxorubicin and cyclophosphamide followed by docetaxel (AC-T) with doxorubicin and cyclophosphamide followed by docetaxel and trastuzumab (AC-TH) and with docetaxel, carboplatin and trastuzumab (TCH) in the adjuvant treatment of node positive and high risk node negative patients with operable breast cancer containing the her2neu alteration (study code BCIRG 006). All of these are very important multicentric and multiinstitutional studies in which several patients have been enrolled.
Deskriptorji     OVARIAN NEOPLASMS
ANTIBODIES, MONOCLONAL
CA-15-3 ANTIGEN
ANTINEOPLASTIC AGENTS, COMBINED
BREAST NEOPLASMS
RADIOIMMUNOTHERAPY
PACLITAXEL
DISEASE-FREE SURVIVAL
TREATMENT OUTCOME