TY - JOUR
T1 - Prognostic significance of an early decline in serum alpha-fetoprotein during chemotherapy for ovarian yolk sac tumors
AU - de la Motte Rouge, Thibault
AU - Pautier, Patricia
AU - Genestie, Catherine
AU - Rey, Annie
AU - Gouy, Sébastien
AU - Leary, Alexandra
AU - Haie-Meder, Christine
AU - Kerbrat, Pierre
AU - Culine, Stéphane
AU - Fizazi, Karim
AU - Lhommé, Catherine
N1 - Publisher Copyright:
© 2016
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Background The ovarian yolk sac tumor (OYST) is a very rare malignancy arising in young women. Our objective was to determine whether an early decline in serum alpha-fetoprotein (AFP) during chemotherapy has a prognostic impact. Methods This retrospective study is based on prospectively recorded OYST cases at Gustave Roussy (Cancer Treatment Center). Survival curves were estimated using the Kaplan-Meier method. The serum AFP decline was calculated with the formula previously developed and validated in male patients with poor prognosis non-seminomatous germ cell tumors. Univariate and multivariate analyses were performed using the log-rank test and logistic regression, respectively. Results Data on AFP were available to calculate an early AFP decline in 57 patients. All patients had undergone surgery followed by chemotherapy. The 5-year overall survival (OS) and event-free survival (EFS) rates were 86% (95% CI: 74%–93%) and 84% (95% CI: 73%–91%), respectively. The disease stage, presence of ascites at presentation, use of the BEP regimen, serum AFP half-life and an early AFP decline were significantly predictive factors for OS and EFS in the univariate analysis. The OS rate was 100% and 49% (95% CI: 26%–72%) in patients with a favorable AFP decline and in those with an unfavorable decline, respectively (p < 0.001). In the multivariate analysis, only the presence of ascites at diagnosis (RR = 7.3, p = 0.03) and an unfavorable early AFP decline (RR = 16.9, p < 0.01) were significant negative predictive factors for OS. Conclusions An early AFP decline during chemotherapy is an independent prognostic factor in patients with OYSTs.
AB - Background The ovarian yolk sac tumor (OYST) is a very rare malignancy arising in young women. Our objective was to determine whether an early decline in serum alpha-fetoprotein (AFP) during chemotherapy has a prognostic impact. Methods This retrospective study is based on prospectively recorded OYST cases at Gustave Roussy (Cancer Treatment Center). Survival curves were estimated using the Kaplan-Meier method. The serum AFP decline was calculated with the formula previously developed and validated in male patients with poor prognosis non-seminomatous germ cell tumors. Univariate and multivariate analyses were performed using the log-rank test and logistic regression, respectively. Results Data on AFP were available to calculate an early AFP decline in 57 patients. All patients had undergone surgery followed by chemotherapy. The 5-year overall survival (OS) and event-free survival (EFS) rates were 86% (95% CI: 74%–93%) and 84% (95% CI: 73%–91%), respectively. The disease stage, presence of ascites at presentation, use of the BEP regimen, serum AFP half-life and an early AFP decline were significantly predictive factors for OS and EFS in the univariate analysis. The OS rate was 100% and 49% (95% CI: 26%–72%) in patients with a favorable AFP decline and in those with an unfavorable decline, respectively (p < 0.001). In the multivariate analysis, only the presence of ascites at diagnosis (RR = 7.3, p = 0.03) and an unfavorable early AFP decline (RR = 16.9, p < 0.01) were significant negative predictive factors for OS. Conclusions An early AFP decline during chemotherapy is an independent prognostic factor in patients with OYSTs.
KW - Alpha-fetoprotein
KW - BEP
KW - Chemotherapy
KW - Endodermal sinus tumor
KW - Germ cell tumor
KW - Malignant ovarian germ cell tumor
UR - http://www.scopus.com/inward/record.url?scp=84990235991&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2016.07.005
DO - 10.1016/j.ygyno.2016.07.005
M3 - Article
C2 - 27401840
AN - SCOPUS:84990235991
SN - 0090-8258
VL - 142
SP - 452
EP - 457
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -