Validation of the geriatric vulnerability score in older patients with ovarian cancer: an analysis from the GCIG-ENGOT-GINECO EWOC-1 study

Older patients with ovarian cancer represent a heterogeneous population. The French National Group of Investigators for the Study of Ovarian and Breast Cancer developed the geriatric vulnerability score (GVS) to identify geriatric parameters predictive of poor outcomes. A prospective validation of t...

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Veröffentlicht in:The Lancet. Healthy longevity 2022-03, Vol.3 (3), p.e176-e185
Hauptverfasser: Falandry, Claire, Pommeret, Fanny, Gladieff, Laurence, Tinquaut, Fabien, Lorusso, Domenica, Mouret-Reynier, Marie-Ange, D'Hondt, Véronique, Mollon-Grange, Delphine, Floquet, Anne, Abadie-Lacourtoisie, Sophie, Brachet, Pierre-Emmanuel, Stefani, Laetitia, Rousseau, Frédérique, Frenel, Jean-Sébastien, Del Piano, Francesco, Komulainen, Marja, Warkus, Thomas, Trédan, Olivier, Pujade-Lauraine, Eric, Freyer, Gilles
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Sprache:eng
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Zusammenfassung:Older patients with ovarian cancer represent a heterogeneous population. The French National Group of Investigators for the Study of Ovarian and Breast Cancer developed the geriatric vulnerability score (GVS) to identify geriatric parameters predictive of poor outcomes. A prospective validation of the GVS was needed. The EWOC-1 study (NCT02001272) was an international, open-label, phase 2, three-arm trial designed according to a two-step process. Patients aged 70 years or older with newly diagnosed stage III or IV ovarian cancer were identified and the GVS determined. Those with a GVS of 3 or greater were randomly assigned to the EWOC-1 trial, stratified by country and surgical outcome, to receive three different carboplatin with or without paclitaxel regimens; those not included in the EWOC-1 trial were followed up in the EWOC-1 registry. External validation of the GVS was a secondary endpoint of the trial. Three validation cohorts were identified: the total population (validation cohort 1 [V1], n=447), the registry-only population (validation cohort 2 [V2], n=327), and the carboplatin–paclitaxel-treated population (validation cohort 3 [V3], n=320). From Dec 11, 2013, to Nov 16, 2018, 447 patients were included in 48 academic centres in six countries; 120 in the EWOC-1 trial and 327 in the EWOC-1 registry. Median follow-up was 19·7 (95% CI 8·5–29·7) months for the total cohort; missing values were low (
ISSN:2666-7568
2666-7568
DOI:10.1016/S2666-7568(22)00002-2