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Simultaneous Durvalumab and Platinum-Based Chemoradiotherapy in Unresectable Stage III Non–Small Cell Lung Cancer: The Phase III PACIFIC-2 Study

  • Jeffrey D. Bradley
  • , Shunichi Sugawara
  • , Ki Hyeong Lee
  • , Gyula Ostoros
  • , Ahmet Demirkazik
  • , Milada Zemanova
  • , Virote Sriuranpong
  • , Ana Caroline Zimmer Gelatti
  • , Juliana Janoski de Menezes
  • , Bogdan Zurawski
  • , Michael Newton
  • , Pratibha Chander
  • , Nan Jia
  • , Zofia F. Bielecka
  • , Mustafa Özgüroğlu
  • , Gustavo Girotto
  • , Fernanda Peria
  • , Gustavo Pinto
  • , Pedro Marchi
  • , Eduardo Silva
  • Ana Gelatti, Gilberto de Castro, Sérgio de Azevedo, Adilson Faccio, Yeni Neron, Thais Almeida, Juliana de Menezes, Milada Zemanova, Ondrej Bilek, Jaromir Roubec, Gyula Ostoros, Zsuzsanna Szalai, Ibolya Laczó, Andrea Fülöp, György Losonczy, Gabriella Gálffy, Hari Goyal, Nirav Asarawala, Satheesh Thungappa, Rajeev L. Krishnappa, Sewanti Limaye, Sankar Srinivasan, Mohamed Sehran, Sushant Mittal, Kartikeya Jain, Shailesh Bondarde, Isamu Okamoto, Hidetoshi Hayashi, Young Hak Kim, Yuichi Sakamori, Kaoru Kubota, Shunichi Sugawara, Makoto Nishio, Toyoaki Hida, Teppei Yamaguchi, Tetsuro Kondo, Juan Vazquez Limón, Froylan López-López, Jorge Alatorre Alexander, Alejandro Molina Alavez, Manuel Magallanes Maciel, Jose Gomez Rangel, Manuel Leiva, Henry Gomez, Natalia Valdiviezo, Paolo Valdez, Vanessa Bermudez, Alejandro Figueroa, Jerry Tan Chun Bing, Marie Grace Dawn Isidro, Cherry Pink Villa, Barbara Domingo, Teresa Sy Ortin, Annielyn Beryl Cornel, Joseph Parra, Rafał Dziadziuszko, Dariusz Kowalski, Bogdan Zurawski, Andrzej Badzio, Ewa Wasilewska-Teśluk, Konstantin Laktionov, Galina Statsenko, Mikhail Dvorkin, Evgeniy Levchenko, Ekaterina Solovyeva, Lyubov Vladimirova, Alexander Arkhipov, Natalia Fadeeva, Valery Breder, Dong Wan Kim, Sang We Kim, Keunchil Park, Ki Hyeong Lee, Sung Sook Lee, Gyeong Won Lee, Virote Sriuranpong, Sarayut Geater, Busyamas Chewaskulyong, Jarin Chindaprasirt, Siriwimon Saichamchan, Ahmet Demirkazik, Hasan Coskun, Tuncay Goksel, Mustafa Erman, Mustafa Özgüroğlu, Muhammed Kaplan, Huyen Phung, Khoi Nguyen, Anh Le, Dinh Tien Nguyen
  • University of Pennsylvania
  • Sendai Kousei Hospital
  • Chungbuk National University Hospital
  • Koranyi National Institute for TB and Pulmonology
  • Ankara University
  • Charles University
  • Faculty of Medicine, Chulalongkorn University
  • Museu de Ciência e Tecnología - PUCRS
  • Hospital Nossa Senhora da Conceição
  • Professor Franciszek Lukaszczyk Oncology Center
  • AstraZeneca Pharmaceuticals LP
  • AstraZeneca
  • AstraZeneca Pharma Poland Sp.z.o.o.
  • Istanbul University—Cerrahpaşa

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

38 Citas (Scopus)

Resumen

PURPOSE – Immunotherapy targeting PD-L1 improves outcomes in patients with unresectable stage III non–small cell lung cancer (NSCLC) and no progression after definitive, concurrent chemoradiotherapy (cCRT). Earlier administration of immunotherapy, simultaneously with cCRT, may improve outcomes further.METHODS – Eligible patients were randomly assigned (2:1) to receive either durvalumab or placebo administered from the start of cCRT. Patients without progression after completing cCRT received consolidation durvalumab or placebo (per initial random assignment) until progression. The primary end point was progression-free survival (PFS) by blinded independent central review. Key secondary end points included objective response rate (ORR), overall survival (OS), the proportion of patients alive at 24 months (OS24), and safety.RESULTS – In total, 328 patients were randomly assigned to receive durvalumab (n = 219) or placebo (n = 109). There was no statistically significant difference with durvalumab versus placebo in PFS (hazard ratio [HR], 0.85 [95% CI, 0.65 to 1.12]; P = .247) or OS (HR, 1.03 [95% CI, 0.78 to 1.39]; P = .823); OS24 was 58.4% versus 59.5%, respectively. Confirmed ORR was 60.7% with durvalumab versus 60.6% with placebo (difference, 0.2% [95% CI, −15.2 to 16.3%]; P = .976). With durvalumab versus placebo, respectively, maximum grade 3 or 4 adverse events (AEs) occurred in 53.4% versus 59.3% of patients, pneumonitis or radiation pneumonitis (group term) in 28.8% (grade ≥3: 4.6%) versus 28.7% (grade ≥3: 5.6%), AEs leading to discontinuation of durvalumab or placebo in 25.6% versus 12.0%, and fatal AEs in 13.7% versus 10.2%.CONCLUSION – Among patients with unresectable stage III NSCLC, durvalumab administered from the start of cCRT failed to demonstrate additional benefit compared with cCRT plus placebo. Consolidation durvalumab following definitive cCRT remains the standard of care in this setting.

Idioma originalInglés
Páginas (desde-hasta)1-14
Número de páginas14
PublicaciónJournal of Clinical Oncology
DOI
EstadoPublicada - 2025

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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