UNcommon EGFR Mutations: International Case Series on Efficacy of Osimertinib in Real-Life Practice in First-LiNe Setting (UNICORN).


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 30 03 2022
revised: 10 09 2022
accepted: 03 10 2022
pubmed: 29 10 2022
medline: 25 1 2023
entrez: 28 10 2022
Statut: ppublish

Résumé

Approximately 10% of EGFR mutations (EGFRmuts) are uncommon (ucEGFRmuts). We aimed to collect real-world data about osimertinib for patients with ucEGFRmuts. This is a multicenter, retrospective study of ucEGFRmut (exon 20 insertions excluded) metastatic NSCLC treated with osimertinib as first EGFR inhibitor. The Response Evaluation Criteria in Solid Tumors and response assessment in neuro-oncology brain metastases brain objective response rate (ORR) were evaluated by the investigators. Median progression-free survival (mPFS), median overall survival, and median duration of response (mDOR) were calculated from osimertinib initiation. Mutations found at resistance were collected. A total of 60 patients were included (22 centers, nine countries), with median age of 64 years, 75% females, and 83% Caucasian. The largest subgroups were G719X (30%), L861Q (20%), and de novo Thr790Met (T790M) (15%). The ORR was 61%, mPFS 9.5 months, mDOR 17.4 months, and median overall survival 24.5 months. Regarding patients with no concurrent common mutations or T790M (group A, n = 44), ORR was 60%, mPFS 8.6 months, and mDOR 11 months. For G719X, ORR was 47%, mPFS 8.8 months, and mDOR 9.1 months. For L861Q, ORR was 80%, mPFS 16 months, and mDOR 16 months. For de novo T790M, ORR was 44%, mPFS 12.7 months, and mDOR 46.2 months. Compound EGFRmut including common mutations had better outcome compared with only ucEGFRmut. For 13 patients with a response assessment in neuro-oncology brain metastases-evaluable brain metastases, brain ORR was 46%. For 14 patients, rebiopsy results were analyzed: four patients with additional EGFR mutation (C797S, D585Y, E709K), three with new TP53 mutation, one with c-Met amplification, one with PIK3CA mutation, and one with neuroendocrine transformation. Osimertinib was found to have an activity in ucEGFRmut with a high rate of disease control systemically and intracranially. Several resistance mechanisms were identified. This report comprises, to the best of our knowledge, the largest data set of its kind.

Identifiants

pubmed: 36307041
pii: S1556-0864(22)01854-8
doi: 10.1016/j.jtho.2022.10.004
pii:
doi:

Substances chimiques

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

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

169-180

Informations de copyright

Copyright © 2022 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Jair Bar (J)

Institute of Oncology, Chaim Sheba Medical Center, Ramat Gan, Israel; School of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: Jair.bar@sheba.gov.il.

Nir Peled (N)

Cancer Center, Soroka University Medical Center, Beer Sheva, Israel; Current Address: Shaare Zedek Medical Center, Jerusalem, Israel.

Shiruyeh Schokrpur (S)

Department of Hematology and Medical Oncology, University of California San Diego School of Medicine, San Diego, California.

Mirjana Wolner (M)

Institute of Oncology, Rambam Medical Center, Haifa, Israel.

Ofer Rotem (O)

Thoracic Cancer Service, Rabin Medical Center Davidoff Cancer Centre, Beilinson Campus, Petah Tikva, Israel.

Nicolas Girard (N)

Thorax Institute, Institut Curie, Paris, France.

Frank Aboubakar Nana (F)

Department of Oncologie thoracique, UCLouvain Brussels Woluwe, Brussels, Belgium.

Sofie Derijcke (S)

Thoracic Oncology, AZ Groeninge Hospital, Kortrijk, Belgium.

Waleed Kian (W)

Cancer Center, Soroka University Medical Center, Beer Sheva, Israel; Current Address: Shaare Zedek Medical Center, Jerusalem, Israel.

Sandip Patel (S)

Department of Hematology and Medical Oncology, University of California San Diego School of Medicine, San Diego, California.

Hadas Gantz-Sorotsky (H)

Institute of Oncology, Chaim Sheba Medical Center, Ramat Gan, Israel; School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Alona Zer (A)

Thoracic Cancer Service, Rabin Medical Center Davidoff Cancer Centre, Beilinson Campus, Petah Tikva, Israel; Current Address: Institute of Oncology, Rambam Medical Center, Haifa, Israel.

Mor Moskovitz (M)

Institute of Oncology, Rambam Medical Center, Haifa, Israel; Current Address: Thoracic Cancer Service, Rabin Medical Center Davidoff Cancer Centre, Beilinson Campus, Petah Tikva, Israel.

Giulio Metro (G)

Medical Oncology, Ospedale S. Maria della Misericordia, Aziendsa Ospedaliera di Perugia, Perugia, Italy.

Yakir Rottenberg (Y)

Oncology Department, Hadassah University Hospital - Ein Kerem, Jerusalem, Israel.

Antonio Calles (A)

Medical Oncology Department, Hospital General Universitario Gregorio Marañon, Madrid, Spain.

Maximilian Hochmair (M)

Department of Respiratory & Critical Care Medicine, Karl Landsteiner Institute of Lung Research & Pulmonary Oncology, Klinik Floridsdorf, Vienna, Austria.

Kristof Cuppens (K)

Department of Pulmonology and Thoracic Oncology, Jessa Ziekenhuis, Hasselt, Belgium.

Lynn Decoster (L)

Pulmonology Department, AZ Turnhout - Campus St. Elisabeth, Turnhout, Belgium.

Martin Reck (M)

Thoracic Oncology Dept., Krankenhaus Grosshansdorf, Grosshansdorf, Germany.

Dror Limon (D)

Current Address: Thoracic Cancer Service, Rabin Medical Center Davidoff Cancer Centre, Beilinson Campus, Petah Tikva, Israel; Oncology, Tel Aviv Sourasky Medical Center-(Ichilov), Tel Aviv, Israel.

Estelamari Rodriguez (E)

Sylvester Comprehensive Cancer Center, University of Miami, Coral Gables, Florida.

Christoforos Astaras (C)

Department of Medical Oncology, Fribourg Cantonal Hospital (HFR), Fribourg, Switzerland; Current Address: Oncology Department, HUG - Hopitaux Universitaires de Geneve, Geneva, Switzerland.

Adrienne Bettini (A)

Department of Medical Oncology, Fribourg Cantonal Hospital (HFR), Fribourg, Switzerland.

Simon Häfliger (S)

Medical Oncology Department, Inselspital - Universitatsklinik fur Medizinische Onkologie, Bern, Switzerland.

Alfredo Addeo (A)

Oncology Department, HUG - Hopitaux Universitaires de Geneve, Geneva, Switzerland.

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