. In the GOG177 study, a phase III trial comparing doxorubicin–cisplatin alone with doxorubicin–cisplatin plus paclitaxel, for the first time, a significantly greater RR (57% versus 34%), PFS interval (median, 8.3 months versus 5.3 months), and OS time (median, 15.3 months versus 12.3 months) with combination chemotherapy using the three-drug paclitaxel–doxorubicin–cisplatin (TAP) regimen were observe
Two studies demonstrated a higher response rate (RR) with the combination of cisplatin and doxorubicin, albeit with a lesser effecton progression-free survival (PFS) and overall survival (OS) than with singleagent doxorubicin.
http://theoncologist.alphamedpress.org/content/15/...26.full.pdf+html
Phase III Trial of Doxorubicin With or Without Cisplatin in Advanced Endometrial Carcinoma: A Gynecologic Oncology Group Study
The overall response rate was higher among patients receiving the combination (42%) compared with patients receiving doxorubicin (25%; P = .004). Median PFS was 5.7 and 3.8 months, respectively, for the combination and single agent. The PFS hazard ratio was 0.736 (95% CI, 0.577 to 0.939; P = .014). Median OS was 9.0 and 9.2 months, respectively, for the combination and single agent.
http://jco.ascopubs.org/content/22/19/3902.long
OS Doxorubicin + cisplatin 12,6 Mon
http://jco.ascopubs.org/content/22/19/3902/T6.expansion.html
Doxorubicin + cisplatin (circadian timed) OS 13.2 Mon
http://jco.ascopubs.org/content/22/19/3902/T6.expansion.html
Hm,........
Die Patientenkriterien bei der Zopt Phase 2 hatten teilweise OS begünstigende Faktoren.
factors independently associated with longer survival included white/Hispanic race, better performance status, stage III disease, no prior radiation therapy, and endometrioid tumor histology
http://theoncologist.alphamedpress.org/content/15/...26.full.pdf+html
Ach das langt schon!!!!!!!!!
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