Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3943146 | Gynecologic Oncology | 2015 | 5 Pages |
•Multi-drug resistance was more likely in women with Type 1 compared to Type II cancer.•Most women with Type I cancer displayed assay sensitivty to at least one chemotherapeutic agent in a chemoresponse assay.•PFS was worse in women with Type II EOC with resistant chemoresponse assay results for carboplatin.
ObjectiveType I epithelial ovarian cancers (EOCs) are reported to be relatively chemoresistant. This study sought to compare pretreatment chemoresponse assays in Type I vs. Type II EOCs.Study design383 women with stage III–IV EOC enrolled in an observational study, with known chemoresponse assay results for 7 common therapeutic agents, were included. Type I EOCs were defined as grade 1 serous/endometrioid cancers and all clear cell/mucinous cancers. Type II EOCs were classified as grade 2–3 serous/endometrioid cancers and undifferentiated cancers. Chemotherapy assay responses were classified as sensitive (S), intermediately sensitive (I), or resistant (R). All patients were treated with platinum/taxane therapy following cytoreductive surgery.ResultsThirty (7.8%) tumors were classified as Type I EOC, and 353 (92.2%) as Type II EOC. Type I patients were younger at the time of diagnosis (median age: 57 vs. 62 years, p = 0.018) and had longer survival compared to Type II patients (mPFS: 25.8 vs. 16.4 months, HR = 1.71, p = 0.042). Eighty-six percent of Type I EOC specimens demonstrated a sensitive chemoresponse assay result to at least 1 agent; 35.7% were pan-S to all 7 agents. After adjusting for stage, debulking status, and type of EOC, multi-drug resistance was twice as likely in women with Type I EOC compared to Type II EOC (pan-R, 14.3% vs. 6.8% (p = 0.268); pan-S, 35.7% vs. 51.2% (p = 0.183)), but did not attain statistical significance.Conclusion(s)The majority of women with Type I EOC displayed assay sensitivity to at least one agent. Given the small sample size these findings need to be evaluated further.