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Real-world outcomes with durvalumab after chemoradiotherapy in patients with unresectable stage III NSCLC: interim analysis of overall survival from PACIFIC-R.
Filippi, A R; Bar, J; Chouaid, C; Christoph, D C; Field, J K; Fietkau, R; Garassino, M C; Garrido, P; Haakensen, V D; Kao, S; Markman, B; McDonald, F; Mornex, F; Moskovitz, M; Peters, S; Sibille, A; Siva, S; van den Heuvel, M; Vercauter, P; Anand, S; Chander, P; Licour, M; de Lima, A R; Qiao, Y; Girard, N.
Afiliación
  • Filippi AR; Radiation Oncology Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo and University of Pavia, Pavia, Italy. Electronic address: andreariccardo.filippi@istitutotumori.mi.it.
  • Bar J; Institute of Oncology, Sheba Medical Centre, Ramat Gan; Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Chouaid C; Service de Pneumologie, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
  • Christoph DC; Department of Medical Oncology, Evang. Kliniken Essen-Mitte, Evang. Huyssens-Stiftung Essen-Huttrop, Essen, Germany.
  • Field JK; Roy Castle Lung Cancer Research Programme, Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
  • Fietkau R; Department of Radiation Oncology, Universitätsklinikum Erlangen, Erlangen, Germany.
  • Garassino MC; Department of Hematology/Oncology, The University of Chicago, Chicago, USA.
  • Garrido P; Medical Oncology Department, Hospital Ramón y Cajal, Universidad de Alcalá, Madrid, Spain.
  • Haakensen VD; Department of Oncology and Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
  • Kao S; Chris O'Brien Lifehouse, Sydney.
  • Markman B; Cabrini Hospital and Monash University, Melbourne, Australia.
  • McDonald F; Lung Unit, The Royal Marsden NHS Foundation Trust, London, UK.
  • Mornex F; Department of Radiation Oncology, Centre Hospitalier Universitaire de Lyon, Lyon, France.
  • Moskovitz M; Rambam Health Care Campus, Haifa, Israel.
  • Peters S; Department of Oncology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
  • Sibille A; Department of Pneumology, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
  • Siva S; Peter MacCallum Cancer Centre and The University of Melbourne, Melbourne, Australia.
  • van den Heuvel M; Department of Pulmonary Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Vercauter P; Department of Pneumology, OLV Hospital Aalst, Aalst, Belgium.
  • Anand S; AstraZeneca, Gaithersburg, USA.
  • Chander P; AstraZeneca, Gaithersburg, USA.
  • Licour M; AstraZeneca, Courbevoie, France.
  • de Lima AR; AstraZeneca, Gaithersburg, USA.
  • Qiao Y; AstraZeneca, Gaithersburg, USA.
  • Girard N; Institut du Thorax Curie Montsouris, Institut Curie, Paris; UVSQ, Paris Saclay, Versailles, France.
ESMO Open ; 9(6): 103464, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38833971
ABSTRACT

BACKGROUND:

Based on the findings of the PACIFIC trial, consolidation durvalumab following platinum-based chemoradiotherapy (CRT) is a global standard of care for patients with unresectable, stage III non-small-cell lung cancer (NSCLC). An earlier analysis from the ongoing PACIFIC-R study (NCT03798535) demonstrated the effectiveness of this regimen in terms of progression-free survival (PFS). Here, we report the first planned overall survival (OS) analysis. PATIENTS AND

METHODS:

PACIFIC-R is an observational/non-interventional, retrospective study of patients with unresectable, stage III NSCLC who started durvalumab (10 mg/kg intravenously every 2 weeks) within an AstraZeneca-initiated early access program between September 2017 and December 2018. Primary endpoints are OS and investigator-assessed PFS, estimated using the Kaplan-Meier method.

RESULTS:

By 30 November 2021, the full analysis set included 1154 participants from 10 countries (median follow-up in censored patients 38.7 months). Median OS was not reached, and the 3-year OS rate was 63.2% (95% confidence interval 60.3% to 65.9%). Three-year OS rates were numerically higher among patients with programmed death-ligand 1 (PD-L1) expression on ≥1% versus <1% of tumor cells (TCs; 67.0% versus 54.4%) and patients who received concurrent CRT (cCRT) versus sequential CRT (sCRT) (64.8% versus 57.9%).

CONCLUSIONS:

PACIFIC-R data continue to provide evidence for the effectiveness of consolidation durvalumab after CRT in a large, diverse, real-world population. Better outcomes were observed among patients with PD-L1 TCs ≥1% and patients who received cCRT. Nevertheless, encouraging outcomes were still observed among patients with TCs <1% and patients who received sCRT, supporting use of consolidation durvalumab in a broad population of patients with unresectable, stage III NSCLC.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Quimioradioterapia / Antineoplásicos Inmunológicos / Neoplasias Pulmonares / Anticuerpos Monoclonales Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Quimioradioterapia / Antineoplásicos Inmunológicos / Neoplasias Pulmonares / Anticuerpos Monoclonales Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article