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Determinants of 5-year survival in patients with advanced NSCLC with PD-L1≥50% treated with first-line pembrolizumab outside of clinical trials: results from the Pembro-real 5Y global registry

Articolo
Data di Pubblicazione:
2025
Abstract:
Background Pembrolizumab monotherapy is an established front-line treatment for advanced non-small cell lung cancer (NSCLC) with programmed cell death-ligand 1 (PD-L1) tumor proportion score (TPS)≥50%. However, real-world data on its long-term efficacy remains sparse. Methods This study assessed 5-year outcomes of first-line pembrolizumab monotherapy in a large, multicenter, real-world cohort of patients with advanced NSCLC and PD-L1 TPS≥50%, referred to as Pembro-real 5Y. Individual patient-level data (IPD) from the experimental arm of the KEYNOTE-024 trial were extracted (KN024 IPD cohort) to compare the long-term outcomes between the two cohorts. To further assess the reproducibility of clinical trial results, we reconstructed the "KN024 look-alike"cohort by excluding patients with an Eastern Cooperative Oncology Group-performance status (ECOG-PS)≥2, those requiring corticosteroids with doses ≥10 mg of prednisolone/equivalent, patients with positive/unknown epidermal growth factor receptor/anaplastic lymphoma kinase genotype, and those with pre-existing autoimmune disease. We additionally provided a hierarchical organization of determinants of long-term benefit through a conditional inference tree analysis. Results The study included 1050 patients from 61 institutions across 14 countries, with a median follow-up of 70.3 months. The 5-year survival rate was 26.9% (95% CI: 23.8% to 30.2%), and median OS was 21.8 months (95% CI: 19.1 to 25.7), while 32 (3.0%) patients who achieved a complete response remained progression-free at the data cut-off. The KN024 look-alike cohort had a 5-year survival rate of 29.3% (95% CI: 25.5% to 33.6%) and a median OS of 27.5 months (95% CI: 22.8 to 31.3). Neither the overall study population nor the KN024 look-alike cohort exhibited significantly different OS compared with the KN024 IPD cohort. By the data cut-off, 1015 patients (96.7%) had permanently discontinued treatment: 659 (64.9%) due to progressive disease, 156 (15.4%) due to toxicity, 77 (7.6%) due to treatment completion, and 106 (10.4%) due to other reasons. Overall, 222 participants (21.1%) were treated for a minimum period of 24 months, among them the 5-year survival rates were: 31.7%, 72.7%, 78.6%, 84.2% for patients who discontinued treatment due to progressive disease, toxicity, treatment completion, and other reasons, respectively. Conclusion This study provides valuable real-world evidence that confirms the long-term efficacy of pembrolizumab outside of clinical trials. Hierarchical organization indicates ECOG-PS, age and PD-L1-TPS as the most important predictors of 5-year survival, potentially informing clinical practice.
Tipologia CRIS:
Articolo su Rivista
Keywords:
Immune Checkpoint Inhibitor; Immunotherapy; Lung Cancer
Elenco autori:
Cortellini, A.; Brunetti, L.; Di Fazio, G. R.; Garbo, E.; Pinato, D. J.; Naidoo, J.; Katz, A.; Loza, M.; Neal, J. W.; Genova, C.; Gettinger, S.; Kim, S. Y.; Jayakrishnan, R.; El Zarif, T.; Russano, M.; Pecci, F.; Di Federico, A.; Awad, M.; Alessi, J. V.; Montrone, M.; Owen, D. H.; Signorelli, D.; Fidler, M. J.; Li, M.; Camerini, A.; De Giglio, A.; Young, L.; Vincenzi, B.; Metro, G.; Passiglia, F.; Yendamuri, S.; Guida, A.; Ghidini, M.; Awosika, N. O.; Napolitano, A.; Fulgenzi, C. A. M.; Grisanti, S.; Grossi, F.; D'Incecco, A.; Josephides, E.; Van Hemelrijck, M.; Russo, A.; Gelibter, A.; Spinelli, G.; Verrico, M.; Tomasik, B.; Giusti, R.; Newsom-Davis, T.; Bria, E.; Sebastian, M.; Rost, M.; Forster, M.; Mukherjee, U.; Landi, L.; Mazzoni, F.; Aujayeb, A.; Dupont, M.; Curioni-Fontecedro, A.; Chiari, R.; Pantano, F.; Morabito, A.; Leonetti, A.; Friedlaender, A.; Addeo, A.; Zoratto, F.; De Tursi, M.; Cantini, L.; Roca, E.; Mountzios, G.; Della Gravara, L.; Kalvapudi, S.; Inno, A.; Bironzo, P.; Di Marco Barros, R.; O'Reilly, D.; Bell, J.; Karapanagiotou, E.; Monnet, I.; Baena, J.; Macerelli, M.; Majem, M.; Agustoni, F.; Cortinovis, D. L.; Tonini, G.; Minuti, G.; Bennati, C.; Mezquita, L.; Gorria, T.; Servetto, A.; Beninato, T.; Lo Russo, G.; Rogado, J.; Moliner, L.; Biello, F.; Aboubakar Nana, F.; Dingemans, A. -M.; Aerts, J. G. J. V.; Ferrara, R.; Torri, V.; Hejleh, T. A.; Takada, K.; Naqash, A. R.; Garassino, M.; Peters, S.; Wakelee, H.; Nassar, A. H.; Ricciuti, B.
Autori di Ateneo:
GHIDINI MICHELE
GROSSI FRANCESCO
oncologia gastrointestinale
Link alla scheda completa:
https://irinsubria.uninsubria.it/handle/11383/2207191
Link al Full Text:
https://irinsubria.uninsubria.it//retrieve/handle/11383/2207191/473209/e010674.full.pdf
Pubblicato in:
JOURNAL FOR IMMUNOTHERAPY OF CANCER
Journal
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