TY - JOUR
T1 - Comparative outcomes assessment of uterine grade 3 endometrioid, serous, and clear cell carcinomas
AU - Ayeni, Tina A.
AU - Bakkum-Gamez, Jamie N.
AU - Mariani, Andrea
AU - McGree, Michaela E.
AU - Weaver, Amy L.
AU - Haddock, Michael G.
AU - Keeney, Gary L.
AU - Long, Harry J.
AU - Dowdy, Sean C.
AU - Podratz, Karl C.
PY - 2013/6
Y1 - 2013/6
N2 - Objective The objective of this study is to assess effects of clinicopathologic risk factors and contemporary therapeutic interventions on high-risk uterine epithelial carcinoma outcomes. Methods Patient-, disease-, and treatment-specific variables were annotated. Survival was estimated via the Kaplan-Meier method. Associations were evaluated with Cox proportional hazard regression and summarized using hazard ratios. Results From 1999 through 2008, therapy with curative intent was initiated for 119 grade 3 endometrioid (G3EC), 211 serous (USC), and 40 clear cell (CCC) carcinomas. Although clinicopathologic risk factors varied among the histologic subtypes, overall survival (OS) did not differ statistically between subtypes (P =.10) or in stage-for-stage comparative analyses (stage I/II, P =.45; stage III, P =.46; stage IV, P =.65). The 5-year cause-specific survival in stage I/II was 84.8%, 89.8%, and 83.9% for G3EC, USC, and CCC, respectively; multivariable modeling identified lymphovascular space involvement (LVSI) as the only independent prognostic factor (P =.02). For stage III, 5-year OS was 49.2% and 40.0% for G3EC and USC, respectively; multivariable modeling identified age (P <.001), LVSI (P <.001), unresectable nodal disease (P =.03), and regional radiotherapy (P =.01) as independent prognostic factors. For stage IV, 5-year OS was 8.7% and 12.1% for G3EC and USC, respectively; multivariable modeling identified LVSI (P =.002), cervical stromal invasion (P =.02), and adjuvant chemotherapy (P =.02) but not residual disease as independent prognostic factors. Conclusions When controlled for disease stage, outcomes did not differ among high-risk histologic subtypes. LVSI was a significant adverse prognostic factor within all stages. The lack of improved outcomes with contemporary therapy suggests that more innovative therapeutic approaches should be given higher priority.
AB - Objective The objective of this study is to assess effects of clinicopathologic risk factors and contemporary therapeutic interventions on high-risk uterine epithelial carcinoma outcomes. Methods Patient-, disease-, and treatment-specific variables were annotated. Survival was estimated via the Kaplan-Meier method. Associations were evaluated with Cox proportional hazard regression and summarized using hazard ratios. Results From 1999 through 2008, therapy with curative intent was initiated for 119 grade 3 endometrioid (G3EC), 211 serous (USC), and 40 clear cell (CCC) carcinomas. Although clinicopathologic risk factors varied among the histologic subtypes, overall survival (OS) did not differ statistically between subtypes (P =.10) or in stage-for-stage comparative analyses (stage I/II, P =.45; stage III, P =.46; stage IV, P =.65). The 5-year cause-specific survival in stage I/II was 84.8%, 89.8%, and 83.9% for G3EC, USC, and CCC, respectively; multivariable modeling identified lymphovascular space involvement (LVSI) as the only independent prognostic factor (P =.02). For stage III, 5-year OS was 49.2% and 40.0% for G3EC and USC, respectively; multivariable modeling identified age (P <.001), LVSI (P <.001), unresectable nodal disease (P =.03), and regional radiotherapy (P =.01) as independent prognostic factors. For stage IV, 5-year OS was 8.7% and 12.1% for G3EC and USC, respectively; multivariable modeling identified LVSI (P =.002), cervical stromal invasion (P =.02), and adjuvant chemotherapy (P =.02) but not residual disease as independent prognostic factors. Conclusions When controlled for disease stage, outcomes did not differ among high-risk histologic subtypes. LVSI was a significant adverse prognostic factor within all stages. The lack of improved outcomes with contemporary therapy suggests that more innovative therapeutic approaches should be given higher priority.
KW - Clinicopathologic prognostic factors
KW - High-risk uterine carcinomas
KW - Outcomes assessment
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U2 - 10.1016/j.ygyno.2013.03.011
DO - 10.1016/j.ygyno.2013.03.011
M3 - Article
C2 - 23535279
AN - SCOPUS:84877584557
SN - 0090-8258
VL - 129
SP - 478
EP - 485
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -