4.7 Article

Survival and modelled cancer antigen-125 ELIMination rate constant K score in ovarian cancer patients in first- line before poly(ADP-ribose) polymerase inhibitor era: A Gynaecologic Cancer Intergroup meta-analysis

Journal

EUROPEAN JOURNAL OF CANCER
Volume 191, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ejca.2023.112966

Keywords

CA-125; KELIM; Ovarian cancer; Primary chemosensitivity; Prognostic biomarker; Surrogate end-point

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In this study, the prognostic and surrogate values of KELIM in advanced ovarian cancer patients were assessed. The results showed that KELIM was associated with overall survival and progression-free survival. Therefore, KELIM can serve as an independent prognostic biomarker and has important implications for treatment success.
Background: In patients with advanced ovarian cancer, the modelled CA-125 ELIMination rate constant K (KELIM) is an early indicator of the tumour intrinsic chemo-sensitivity. We assessed the prognostic and surrogate values of KELIM with respect to those of surgery outcome (based on post-operative residual lesions) in the Gynaecologic Cancer Intergroup (GCIG) individual patient data meta-analysis MAOV (Meta-Analysis in OVarian cancer) built before the emergence of poly(ADP-ribose) polymerase (PARP) inhibitors. Methods: The dataset was split into learning and validation cohorts (ratio 1:2). The in-dividual modelled KELIM values were estimated, standardised by the median value, then scored as unfavourable (< 1.0) or favourable (& GE;1.0). Overall survival (OS) and progression -free survival (PFS) analyses were performed with a two-step meta-analytic approach and surrogacy through a two-level meta-analytic model.Results: KELIM was assessed in 5884 patients from eight first-line trials (learning, 1962; validation, 3922). A favourable KELIM score was significantly associated with longer OS (validation set, median, 78.8 versus 28.4 months, hazard-ratios [HR] 0.46, 95% confidence interval [CI], 0.41-0.50, C-index 0.68), and longer PFS (validation set, median 30.5 versus 9.8 months, HR 0.49, 95% CI, 0.45-0.54, C-index 0.68), as were International Federation of Gynaecology and Obstetrics (FIGO) stage and debulking surgery outcome. Three prognostic groups were identified based on the surgery outcome and KELIM score, with large differences in OS (105.1, & SIM;45.0, and 22.1 months) and PFS (58.1, & SIM;15.0, and 8.0 months). Surrogacy for OS and for PFS was not established.Conclusion: KELIM is an independent prognostic biomarker for survival, complementary to surgery outcome, representing a new determinant of first-line treatment success.& COPY; 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC 4.0 (http://creativecommons.org/licenses/by-nc/4.0/).

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