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

Alessio Cortellini(Università Campus Bio-Medico), Leonardo Brunetti(Università Campus Bio-Medico), Giuseppina Rita Di Fazio(Università Campus Bio-Medico), Edoardo Garbo(Dana-Farber Cancer Institute), David J. Pinato(Università degli Studi del Piemonte Orientale “Amedeo Avogadro”), Jarushka Naidoo(Johns Hopkins University), Artur Katz(Hospital Sírio-Libanês), Monica Loza(Stanford University), Joel W. Neal(Stanford University), Carlo Genova(Ospedale Policlinico San Martino), Scott Gettinger(Yale Cancer Center), So Yeon Kim(Yale Cancer Center), Ritujith Jayakrishnan(Yale Cancer Center), Talal El Zarif(Yale Cancer Center), Marco Russano(Campus Bio Medico University Hospital), Federica Pecci(Dana-Farber Cancer Institute), Alessandro Di Federico(Dana-Farber Cancer Institute), Mark M. Awad(Dana-Farber Cancer Institute), Joao V. Alessi(Dana-Farber Cancer Institute), Michele Montrone(Istituto Tumori Bari), Dwight H. Owen(The Ohio State University), Diego Signorelli(Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda), Mary J. Fidler(Rush University Medical Center), Mingjia Li(The Ohio State University), Andrea Camerini(Ospedale Versilia), Andrea De Giglio(University of Bologna), Lauren Young(Albert Einstein College of Medicine), Bruno Vincenzi(Università Campus Bio-Medico), Giulio Metro(Azienda Ospedaliera di Perugia), Francesco Passiglia(University of Turin), Sai Yendamuri(Roswell Park Comprehensive Cancer Center), Annalisa Guida(Azienda Ospedaliera S.Maria), Michele Ghidini(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Nichola Awosika(Hammersmith Hospital), Andrea Napolitano(Royal Marsden NHS Foundation Trust), Claudia A M Fulgenzi(Hammersmith Hospital), Salvatore Grisanti(University of Brescia), Francesco Grossi(University of Insubria), Armida D’Incecco(University of Teramo), Eleni Josephides(St Thomas' Hospital), Mieke Van Hemelrijck(St Thomas' Hospital), Alessandro Russo, Alain Gelibter(Sapienza University of Rome), Gianpaolo Spinelli, Monica Verrico(Policlinico Umberto I), Bartłomiej Tomasik(Gdańsk Medical University), Raffaele Giusti(CTO Andrea Alesini), Thomas Newsom-Davis(Chelsea and Westminster Hospital), Emilio Bria(Università Cattolica del Sacro Cuore), Martin Sebastian(Goethe University Frankfurt), Maximilian Rost(Goethe University Frankfurt), Martin Förster(University College London Hospitals NHS Foundation Trust), Uma Mukherjee(University College London Hospitals NHS Foundation Trust), Lorenza Landi, Francesca Mazzoni(Azienda Ospedaliero-Universitaria Careggi), Avinash Aujayeb(Northumbria Healthcare NHS Foundation Trust), Manuel Dupont(University of Fribourg), Alessandra Curioni‐Fontecedro(University of Fribourg), Rita Chiari, Francesco Pantano(Università Campus Bio-Medico), Alessandro Morabito(Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale"), Alessandro Leonetti(University of Parma), Alex Friedlaender(Générale-Beaulieu Clinic), Alfredo Addeo(University Hospital of Geneva), Federica Zoratto(Ospedale Santa Maria Goretti), Michele De Tursi(University of Chieti-Pescara), Luca Cantini, Elisa Roca, Giannis Mountzios(Henry Dunant Hospital), Luigi Della Gravara(Ospedale Monaldi), Sukumar Kalvapudi(Roswell Park Comprehensive Cancer Center), Alessandro Inno(Ospedale Sacro Cuore Don Calabria), Paolo Bironzo(University of Turin), Rafael Di Marco Barros(St Thomas' Hospital), David O’Reilly(Beaumont Hospital), Jack Bell(Beaumont Hospital), Eleni Karapanagiotou(St Thomas' Hospital), Isabelle Monnet(Hôpital Intercommunal de Créteil), Javier Baena Preysler(Hospital Universitario 12 De Octubre), Marianna Macerelli(Ospedale Santa Maria della Misericordia di Udine), Margarita Majem(Hospital de Sant Pau), Francesco Agustoni(Policlinico San Matteo Fondazione), Diego Cortinovis(Azienda Ospedaliera San Gerardo), Giuseppe Tonini(Università Campus Bio-Medico), Gabriele Minuti, Chiara Bennati(Azienda Unità Sanitaria Locale Della Romagna), Laura Mezquita(Hospital Clínic de Barcelona), Teresa Gorría(Hospital Clínic de Barcelona), Alberto Servetto(University of Naples Federico II), Teresa Beninato(Fondazione IRCCS Istituto Nazionale dei Tumori), Giuseppe Lo Russo(Fondazione IRCCS Istituto Nazionale dei Tumori), Jacobo Rogado(Hospital Universitario Infanta Leonor), Laura Moliner(Institut Català d'Oncologia), Federica Biello(Università degli Studi del Piemonte Orientale “Amedeo Avogadro”), Frank Aboubakar Nana(Cliniques Universitaires Saint-Luc), Anne‐Marie C. Dingemans(Erasmus MC Cancer Institute), Joachim G.J.V. Aerts(Erasmus MC Cancer Institute), Roberto Ferrara(Vita-Salute San Raffaele University), Valter Torri(Mario Negri Institute for Pharmacological Research), Taher Abu Hejleh(University of Iowa), Kazuki Takada(Saiseikai Fukuoka General Hospital), Abdul Rafeh Naqash(University of Oklahoma Medical Center), Marina Chiara Garassino(University of Chicago), Solange Peters(University Hospital of Lausanne), Heather Wakelee(Stanford University), Amin H Nassar(Yale Cancer Center), Biagio Ricciuti(Dana-Farber Cancer Institute)
Journal for ImmunoTherapy of Cancer
February 1, 2025
Cited by 21Open Access
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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.


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