Heterogeneity of progression-free-survival surrogacy by sex in randomized trials testing immunotherapy in NSCLC
Menée à partir de l'analyse des résultats de 20 essais cliniques randomisés incluant au total 7 528 patients et 3 008 patientes atteints d'un cancer du poumon non à petites cellules de stade avancé traité par inhibiteur de point de contrôle immunitaire en combinaison ou non avec une chimiothérapie, cette étude examine, en fonction du sexe, la fiabilité de la survie sans progression comme critère de jugement de substitution à la survie globale
Background : The surrogacy of progression-free survival (PFS) for overall survival (OS) at the trial-level in randomized clinical trials (RCTs) testing immune checkpoint inhibitors (ICIs) in patients with advanced non-small cell lung cancers (NSCLC) is influenced by several clinical-pathological factors. However, potential heterogeneity of PFS surrogacy according to patients’ sex has never been investigated.
Methods : RCTs testing ICIs as monotherapy or combined with chemotherapy in patients with advanced NSCLC reporting hazard ratios (HR) for PFS and OS according to patients’ sex were included.
The main objective was to assess sex-based heterogeneity in the trial-level association between PFS (surrogate endpoint) and OS (reference endpoint), overall and in subgroups defined by treatment type (ICIs as monotherapy vs ICIs plus chemotherapy). We used the coefficient of determination (R2) to quantify surrogacy.
Results : Twenty RCTs, for a total of 7,528 male and 3,008 female patients, were included.
Overall, the association between OS-HR and PFS-HR was moderate: the R2 from a model adjusted by the type of treatment administered in the experimental arm was 0.69 (95% CI, 0.34 to 0.88). Sex-disaggregated analysis showed heterogeneity in PFS surrogacy: the association was strong in male (adjusted R2=0.77; 95% CI, 0.56 to 0.89), but poor in female (adjusted R2=0.31; 95% CI, 0.03 to 0.63). Consistent results were obtained in subgroups analyses by treatment type, and in cross validation analysis.
Conclusions : In RCTs testing ICIs alone or combined with chemotherapy in patients with advanced NSCLC, PFS is a robust surrogate endpoint for OS in male but not in female.
JNCI Cancer Spectrum , article en libre accès, 2025