Osimertinib Maintenance After Definitive Chemoradiation in Patients With Unresectable EGFR Mutation Positive Stage III Non-small-cell Lung Cancer: LAURA Trial in Progress.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
07 2021
Historique:
received: 02 09 2020
revised: 22 10 2020
accepted: 16 11 2020
pubmed: 10 2 2021
medline: 7 1 2022
entrez: 9 2 2021
Statut: ppublish

Résumé

The LAURA trial (NCT03521154) will evaluate the efficacy and safety of osimertinib as maintenance therapy in patients with locally advanced, unresectable, epidermal growth factor receptor mutation-positive (EGFRm), stage III non-small-cell lung cancer (NSCLC) without disease progression during/following definitive platinum-based chemoradiation therapy (CRT). Eligible patients include adults aged ≥ 18 years (≥ 20 years in Japan) with locally advanced, unresectable, stage III NSCLC with local/central confirmation of an EGFR exon 19 deletion/L858R mutation. Patients must have received ≥ 2 cycles of concurrent/sequential platinum-based CRT, have no investigator-assessed progression, and have creatinine < 1.5 × upper limit of normal and creatinine clearance ≥ 30 mL/min. In this phase III trial, patients will be randomized 2:1 to once-daily osimertinib 80 mg or placebo, until objective radiological disease progression per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1, confirmed by blinded independent central review (BICR). The primary objective is to assess the efficacy of osimertinib per BICR-confirmed progression-free survival (PFS). Secondary objectives include central nervous system PFS, overall survival, PFS by mutation status and safety. Patients with BICR-confirmed disease progression (or investigator-confirmed progression if after primary PFS analysis) may be unblinded and receive open-label osimertinib; all will have post-progression follow-up. Serious adverse events and adverse events of special interest will be collected throughout the trial and survival follow-up. The first patient was enrolled in July 2018, with results expected in late 2022.

Identifiants

pubmed: 33558193
pii: S1525-7304(20)30337-5
doi: 10.1016/j.cllc.2020.11.004
pii:
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
Protein Kinase Inhibitors 0
osimertinib 3C06JJ0Z2O
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT03521154']

Types de publication

Clinical Trial Protocol Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

371-375

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Shun Lu (S)

Lung Cancer Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China. Electronic address: shunlu@me.com.

Ignacio Casarini (I)

Servicio Oncología, Clínica y Maternidad Colón SAA, Mar del Plata, Buenos Aires, Argentina.

Terufumi Kato (T)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.

Manuel Cobo (M)

Unidad de Gestión Clínica Intercentros de Oncología Médica, Hospitales Universitarios Regional y Virgen de la Victoria, IBIMA, Málaga, Spain.

Mustafa Özgüroğlu (M)

Department of Internal Medicine, Division of Medical Oncology Clinical Trial Unit, Istanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, Istanbul, Turkey.

Rachel Hodge (R)

Oncology Biometrics, AstraZeneca, Cambridge, UK.

Toon van der Gronde (T)

Late Oncology, Oncology R&D, AstraZeneca, Cambridge, UK.

Matilde Saggese (M)

Late Oncology, Oncology R&D, AstraZeneca, Cambridge, UK.

Suresh S Ramalingam (SS)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Winship Cancer Institute, Atlanta, GA.

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Classifications MeSH