TY - JOUR
T1 - Prognostic significance of ethnicity and age in advanced stage epithelial ovarian cancer
T2 - An NRG oncology/gynecologic oncology group study
AU - duPont, Nefertiti C.
AU - Enserro, Danielle
AU - Brady, Mark F.
AU - Moxley, Katherine
AU - Walker, Joan L.
AU - Cosgrove, Casey
AU - Bixel, Kristin
AU - Tewari, Krishnansu S.
AU - Thaker, Premal
AU - Wahner Hendrickson, Andrea E.
AU - Rubin, Stephen
AU - Fujiwara, Keiichi
AU - Casey, A. Catherine
AU - Soper, John
AU - Burger, Robert A.
AU - Monk, Bradley J.
N1 - Publisher Copyright:
© 2021
PY - 2022/2
Y1 - 2022/2
N2 - Background: Age and ethnicity are among several factors that influence overall survival (OS) in ovarian cancer. The study objective was to determine whether ethnicity and age were of prognostic significance in women enrolled in a clinical trial evaluating the addition of bevacizumab to front-line therapy. Methods: Women with advanced stage ovarian, primary peritoneal, or fallopian tube cancer were enrolled in a phase III clinical trial. All women had surgical staging and received adjuvant chemotherapy with one of three regimens. Cox proportional hazards models were used to evaluate the relationship between OS with age and race/ethnicity among the study participants. Results: One-thousand-eight-hundred-seventy-three women were enrolled in the study. There were 280 minority women and 328 women over the age of 70. Women age 70 and older had a 34% increase risk for death when compared to women under 60 (HR = 1.34; 95% CI 1.16–1.54). Non-Hispanic Black women had a 54% decreased risk of death with the addition of maintenance bevacizumab (HR = 0.46, 95% CI:0.26–0.83). Women of Asian descent had more hematologic grade 3 or greater adverse events and a 27% decrease risk of death when compared to non-Hispanic Whites (HR = 0.73; 95% CI: 0.59–0.90). Conclusions: Non-Hispanic Black women showed a decreased risk of death with the addition of bevacizumab and patients of Asian ancestry had a lower death rate than all other minority groups, but despite these clinically meaningful improvements there was no statistically significant difference in OS among the groups.
AB - Background: Age and ethnicity are among several factors that influence overall survival (OS) in ovarian cancer. The study objective was to determine whether ethnicity and age were of prognostic significance in women enrolled in a clinical trial evaluating the addition of bevacizumab to front-line therapy. Methods: Women with advanced stage ovarian, primary peritoneal, or fallopian tube cancer were enrolled in a phase III clinical trial. All women had surgical staging and received adjuvant chemotherapy with one of three regimens. Cox proportional hazards models were used to evaluate the relationship between OS with age and race/ethnicity among the study participants. Results: One-thousand-eight-hundred-seventy-three women were enrolled in the study. There were 280 minority women and 328 women over the age of 70. Women age 70 and older had a 34% increase risk for death when compared to women under 60 (HR = 1.34; 95% CI 1.16–1.54). Non-Hispanic Black women had a 54% decreased risk of death with the addition of maintenance bevacizumab (HR = 0.46, 95% CI:0.26–0.83). Women of Asian descent had more hematologic grade 3 or greater adverse events and a 27% decrease risk of death when compared to non-Hispanic Whites (HR = 0.73; 95% CI: 0.59–0.90). Conclusions: Non-Hispanic Black women showed a decreased risk of death with the addition of bevacizumab and patients of Asian ancestry had a lower death rate than all other minority groups, but despite these clinically meaningful improvements there was no statistically significant difference in OS among the groups.
KW - African American women
KW - Asian women
KW - Bevacizumab
KW - Elderly
KW - Minority populations
KW - Ovarian cancer
UR - http://www.scopus.com/inward/record.url?scp=85122958550&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2021.11.013
DO - 10.1016/j.ygyno.2021.11.013
M3 - Article
C2 - 34857397
AN - SCOPUS:85122958550
SN - 0090-8258
VL - 164
SP - 398
EP - 405
JO - Gynecologic oncology
JF - Gynecologic oncology
IS - 2
ER -