Prognostic factors and overall survival among patients with ovarian cancer in the pre-PARP inhibitor era: the OCRWE-Finland study

Authors

  • Mari Lahelma Nordic Healthcare Group, Helsinki, Finland
  • Heini Rauhamaa Nordic Healthcare Group, Helsinki, Finland; Terveystalo
  • Riikka-Leena Leskelä Nordic Healthcare Group, Helsinki, Finland
  • Outi Isomeri Nordic Healthcare Group, Helsinki, Finland https://orcid.org/0009-0009-8460-8913
  • Juhana Idänpään-Heikkilä GSK, Helsinki, Finland
  • Sari Käkelä GSK, Helsinki, Finland
  • Nichola Roebuck GSK, Brentford, Middlesex, UK; ImmunoGen, Inc
  • Barbara Mascialino GSK, Verona, Italy
  • Sakari Hietanen Department of Gynecologic Oncology, Turku University Hospital and FICAN West, Turku, Finland
  • Mikko Loukovaara Department of Obstetrics and Gynecology and Comprehensive Cancer Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland
  • Annika Auranen Department of Obstetrics and Gynecology, Tays Cancer Centre, Tampere University Hospital and Tampere University, Tampere, Finland

DOI:

https://doi.org/10.2340/1651-226X.2024.40324

Keywords:

Ovarian cancer, high-grade serous ovarian cancer, real-world evidence, overall survival, neoadjuvant chemotherapy, bevacizumab, prognostic factors

Abstract

Background: Despite recent treatment advances in ovarian cancer (OC), more real-world evidence studies investigating patient outcomes are needed. OCRWE-Finland was an observational cohort study investigating OC outcomes in Finland during the pre-PARP inhibitor era.

Patients: Patients were diagnosed with OC between 2014 and 2019 in Finland. This analysis reports baseline characteristics of all patients, patients with high-grade serous OC (HGSOC), and overall survival (OS) for patients with HGSOC.

Results: Among 1,711 patients diagnosed with OC, 867 (51%) had HGSOC. The absence versus presence of visible residual disease post-debulking surgery was associated with improved OS for patients at stage III (n = 303; median: NR vs. 43 months; p = 0.005), but not stage IV (n = 118; median: 37 months vs. 40 months; p = 0.96). Bevacizumab treatment at any line at stages III/IV improved OS in the short-term only. Receiving versus not receiving bevacizumab at first-line for patients with visible residual disease post-debulking surgery was associated with improved OS at stage III (median: 48 months vs. 36 months; p = 0.003), but not stage IV (median: 42 months vs. 37 months; p = 0.26). Multivariate Cox regression analyses showed that stage IV at initial diagnosis and the presence of R2 classification post-debulking surgery resulted in poorer OS.

Interpretation: In the pre-PARP inhibitor era, the absence versus presence of visible residual disease post-debulking surgery was associated with improved OS in stage III, but not stage IV HGSOC. First-line bevacizumab seemed to be beneficial in patients with stage III HGSOC and visible residual disease.

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Additional Files

Published

2024-10-16

How to Cite

Lahelma, M., Rauhamaa, H., Leskelä, R.-L., Isomeri, O., Idänpään-Heikkilä, J., Käkelä, S., … Auranen, A. (2024). Prognostic factors and overall survival among patients with ovarian cancer in the pre-PARP inhibitor era: the OCRWE-Finland study. Acta Oncologica, 63(1), 763–771. https://doi.org/10.2340/1651-226X.2024.40324