TY - JOUR
T1 - Hormonal maintenance therapy for women with low-grade serous cancer of the ovary or peritoneum
AU - Gershenson, David M.
AU - Bodurka, Diane C.
AU - Coleman, Robert L.
AU - Lu, Karen H.
AU - Malpica, Anais
AU - Sun, Charlotte C.
N1 - Publisher Copyright:
© 2017 by American Society of Clinical Oncology.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Purpose The purpose of this study was to examine outcomes associated with hormonal maintenance therapy (HMT) comparedwith routine observation (OBS) after primary cytoreductive surgery and platinum-based chemotherapy in women with stage II to IV low-grade serous carcinoma of the ovary or peritoneum. Patients and Methods Eligibility criteria for patients from our databasewere: treatment with primary surgery followed by platinumbased chemotherapy, stage II to IV disease, at least 2 years of follow-up for patients who had not experienced recurrence, and adequate clinical information. The two groups were compared for progressionfree survival (PFS) and overall survival, and a multivariable Cox regression analysis was performed. Subset analyses for patients who were disease free or had persistent disease were also performed. Results Between 1981 and 2013, 203 eligible patients-133 who underwent OBS and 70 who received HMT-were seen at our institution.Median PFS for patients who underwent OBS was 26.4 months, compared with 64.9 months for those who received HMT (P, .001). No statistically significant difference in overall survival was observed between the two groups (102.7 v 115.7 months, respectively). For subgroups of women who were disease free or had persistent disease, median PFS was superior for those who received HMT (81.1 v 30.0 months; P, .001 and 38.1 v 15.2 months; P, .001, respectively). Women who received HMT had a significantly lower risk of disease progression compared with thosewho underwentOBS (hazard ratio, 0.44; 95%CI, 0.31 to 0.64; P,.001). Conclusion Women with stage II to IV low-grade serous carcinoma who received HMT after primary treatment had significantly longer PFS compared with women who underwent OBS. These findings warrant further investigation using a prospective trial design.
AB - Purpose The purpose of this study was to examine outcomes associated with hormonal maintenance therapy (HMT) comparedwith routine observation (OBS) after primary cytoreductive surgery and platinum-based chemotherapy in women with stage II to IV low-grade serous carcinoma of the ovary or peritoneum. Patients and Methods Eligibility criteria for patients from our databasewere: treatment with primary surgery followed by platinumbased chemotherapy, stage II to IV disease, at least 2 years of follow-up for patients who had not experienced recurrence, and adequate clinical information. The two groups were compared for progressionfree survival (PFS) and overall survival, and a multivariable Cox regression analysis was performed. Subset analyses for patients who were disease free or had persistent disease were also performed. Results Between 1981 and 2013, 203 eligible patients-133 who underwent OBS and 70 who received HMT-were seen at our institution.Median PFS for patients who underwent OBS was 26.4 months, compared with 64.9 months for those who received HMT (P, .001). No statistically significant difference in overall survival was observed between the two groups (102.7 v 115.7 months, respectively). For subgroups of women who were disease free or had persistent disease, median PFS was superior for those who received HMT (81.1 v 30.0 months; P, .001 and 38.1 v 15.2 months; P, .001, respectively). Women who received HMT had a significantly lower risk of disease progression compared with thosewho underwentOBS (hazard ratio, 0.44; 95%CI, 0.31 to 0.64; P,.001). Conclusion Women with stage II to IV low-grade serous carcinoma who received HMT after primary treatment had significantly longer PFS compared with women who underwent OBS. These findings warrant further investigation using a prospective trial design.
UR - http://www.scopus.com/inward/record.url?scp=85016560368&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85016560368&partnerID=8YFLogxK
U2 - 10.1200/JCO.2016.71.0632
DO - 10.1200/JCO.2016.71.0632
M3 - Article
C2 - 28221866
AN - SCOPUS:85016560368
SN - 0732-183X
VL - 35
SP - 1103
EP - 1111
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 10
ER -