Abstract

Investigate the clinical landscape of ovarian carcinoma (OC) over time. Register-based prospectively collected data. South East Scotland. A total of 2805 OC patients diagnosed in 1981-2015. Survival times were visualised using the Kaplan-Meier method; median survival, 5-year survival probabilities and associated restricted mean survival time analyses were used to quantify survival differences. Disease-specific survival. A significant increase in disease-specific survival (DSS) from 1981-1985 to 2011-2015 was observed (median 1.73 versus 4.23years, P<0.0001). Corresponding increase in progression-free survival (PFS) was not statistically significant (median 1.22 versus 1.58years, P=0.2568). An increase in the proportion of cases with low residual disease volume (RD) (<2cm RD) following debulking was observed (54.0% versus 87.7%, P<0.0001). The proportion of high grade serous (HGS) cases increased (P<0.0001), whereas endometrioid and mucinous cases decreased (P=0.0005 and P=0.0002). Increases in stage IV HGS OCincidence (P=0.0009) and stage IV HGSOC DSS (P=0.0122) were observed. Increasing median age at diagnosis correlated with increasing Eastern Cooperative Oncology Group Performance Status (ECOG PS) over time (r=0.86). OC DSS has improved over the last 35years. PFS has not significantly increased, highlighting that improvement in outcome has been limited to extending post-relapse survival. Distribution of stage at diagnosis, histological subtype and RD following debulking has changed over time, reflecting evolution in tumour classification, staging and optimal debulking definitions (from low RD to minimal or zero RD). Histology, stage, RD and ECOG PS remain reliable outcome predictors. Increasing median age at diagnosis and ECOG PS indicates demographic shifts in the clinical population. Significant improvement in ovarian carcinoma survival has been seen over time. Most of this improvement is due to an extension of survival following disease relapse.

Highlights

  • With over 290, 000 new diagnoses and 180, 000 deaths per year worldwide, ovarian cancer is the most lethal of all gynaecological malignancies[1]

  • It is recognised that ovarian carcinoma (OC) - which represents around 90% of ovarian cancer cases - is a collection of discrete diseases, the five main histotypes of which are high grade serous (HGS), endometrioid, clear cell (CC), mucinous and low grade serous (LGS) OC3

  • All pathologically confirmed epithelial OC diagnoses of serous, mucinous, endometrioid or clear cell histological type between 1981-2015 were included (Figure S1), including cases recorded as primary fallopian tube or primary peritoneal carcinoma, representing the vast majority of OC cases in the region

Read more

Summary

Introduction

With over 290, 000 new diagnoses and 180, 000 deaths per year worldwide, ovarian cancer is the most lethal of all gynaecological malignancies[1]. It is recognised that ovarian carcinoma (OC) - which represents around 90% of ovarian cancer cases - is a collection of discrete diseases, the five main histotypes of which are high grade serous (HGS), endometrioid, clear cell (CC), mucinous and low grade serous (LGS) OC3. These histotypes display chemosensitivity, typical stage at diagnosis and overall survival outcome[4]. These histotypes are known to arise from distinct gynaecological sites[5,6,7,8,9]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call