Advanced stage mucinous epithelial ovarian cancer: The Hellenic Cooperative Oncology Group experience

Mucinous epithelial ovarian cancer (mEOC) representing about 10% of all EOC are known to be possibly resistant to platinum-based chemotherapy and bear a poorer prognosis with respect to other subtypes of EOC. This study was undertaken to compare response and survival to platinum-based chemotherapy b...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Gynecologic oncology 2005-05, Vol.97 (2), p.436-441
Hauptverfasser: Pectasides, Dimitrios, Fountzilas, George, Aravantinos, Gerasimos, Kalofonos, Haralampos P., Efstathiou, Eleni, Salamalekis, Emmanouel, Farmakis, Dimitrios, Skarlos, Dimosthenis, Briasoulis, Evangelos, Economopoulos, Theofanis, Dimopoulos, Meletios A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Mucinous epithelial ovarian cancer (mEOC) representing about 10% of all EOC are known to be possibly resistant to platinum-based chemotherapy and bear a poorer prognosis with respect to other subtypes of EOC. This study was undertaken to compare response and survival to platinum-based chemotherapy between patients with advanced stages III and IV mEOC and serous EOC (sEOC). A retrospective analysis was performed in 47 patients with advanced stage of mEOC treated with first-line platinum-based chemotherapy in the context of several study protocols of the Hellenic Cooperative Oncology Group (HeCOG) between 6/7/1983 and 25/2/2003. The outcome was compared to that of 94 patients with sEOC treated with the same protocols during the same study period (ratio mucinous: serous 1:2). One hundred forty-one patients (47 stages III and IV mEOC, 94 stages III and IV sEOC) treated with platinum-based chemotherapy were analyzed. The overall response rate for mEOC was 38.5% (complete remission 18%) (95% CI 23.4–55.4%) and 70% (complete remission 47%) (95% CI 58.5–80.3%) for sEOC ( P = 0.001). After a median follow-up of 77.8 months, median survival and time to tumor progression (TTP) were not significantly different between the two groups (33.2 months [95% CI 23.3–43.1 months] vs. 38.0 months [95% CI 26.8–49.2 months], P = 0.46, 11.8 months [95% CI 7.2–16.4 months] vs. 20.0 months [95% CI 15.7–24.2 months], P = 0.18, respectively). Patients with mEOC have significantly lower response to first-line platinum-based chemotherapy compared to patients with sEOC. This low response to platinum-based chemotherapy was not translated in inferior TTP or survival. Our data indicate that a new strategy for chemotherapy in mEOC should be adopted, one that focuses on new agents without cross-resistance to platinum agents.
ISSN:0090-8258
1095-6859
DOI:10.1016/j.ygyno.2004.12.056