Evidence map›Paper›PMID 36129569›Full record

ArticleTargeted oncology2022

Histomolecular Resistance Mechanisms to First-Line Osimertinib in EGFR-Mutated Advanced Non-Small Cell Lung Cancer: A Multicentric Retrospective French Study.

Assya Akli, Nicolas Girard, Vincent Fallet, Gaelle Rousseau-Bussac, Valérie Gounant, Sylvie Friard, Jean Trédaniel, Cécile Dujon, Marie Wislez, Boris Duchemann and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Targeted oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Analysis of genomic alternations in epidermal growth factor receptor (EGFR)-T790M-mutated non-small cell lung cancer (NSCLC) patients with acquired resistance to osimertinib therapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  5. Transitional CXCL14Clinical and translational medicine · 2025
    Article
  6. Observational
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 10 institutions in 1 country.

Assya AkliDepartment of Respiratory Diseases and Thoracic Oncology, APHP-Hopital Ambroise Pare, Paris-Saclay University, UVSQ, 9 avenue Charles de Gaulle, 92100, Boulogne-Billancourt, France.
Nicolas GirardInstitute Curie, Thorax Institute, Paris-Saclay University, UVSQ, Paris, France.
Vincent FalletDepartment of Pneumology and Thoracic Oncology, APHP-Hopital Tenon, Sorbonne University, Paris, France.
Gaelle Rousseau-BussacChest Department, Creteil Intercommunal Hospital, Créteil, France.
Valérie GounantThoracic Oncology Department, Paris-Cité University, APHP-Hopital Bichat, Paris, France.
Sylvie FriardPneumology Department, Foch Hospital, Suresnes, France.
Jean TrédanielPneumology Department, Saint-Joseph Hospital, Paris, France.
Cécile DujonPneumology Department, André Mignot Hospital, Le Chesnay, France.
Marie WislezDepartment of Pulmonology, Thoracic Oncology Unit, APHP-Hopital Cochin, Paris-Cité University, Paris, France.
Boris DuchemannDepartment of Medical Oncology, APHP-Hopital Avicenne, Sorbonne Paris Nord University, Bobigny, France.
Etienne Giroux-LeprieurDepartment of Respiratory Diseases and Thoracic Oncology, APHP-Hopital Ambroise Pare, Paris-Saclay University, UVSQ, 9 avenue Charles de Gaulle, 92100, Boulogne-Billancourt, France. etienne.giroux-leprieur@aphp.fr.
Assistance Publique – Hôpitaux de Paris · FRHôpital André Mignot · FRHôpital Foch · FRHôpital Intercommunal de Créteil · FRHôpital Paris Saint-Joseph · FRHôpital Tenon · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FRUniversité Paris Cité · FRUniversité Paris-Saclay · FRUniversité Sorbonne Paris Nord · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsimertinib is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) used in first line for the treatment of advanced EGFR-mutated non-small cell lung cancer (NSCLC).

objectiveThe identification of related histomolecular resistance mechanisms to first-line osimertinib is a critical step to define the optimal treatment strategy beyond progression. PATIENTS AND

methodsAll consecutive patients treated in the first line with osimertinib for advanced EGFR-mutated NSCLC at 10 hospitals in the Greater Paris area between April 2015 and January 2021 were included. Histomolecular data from plasma and tissue samples taken at progression under osimertinib were collected, and all samples were analyzed using DNA next-generation sequencing. Data on objective response rate (ORR), overall survival (OS), progression-free survival (PFS), and time to treatment discontinuation (TTD) were also collected.

resultsOverall, 104 patients were included. Most patients had adenocarcinoma (n = 102, 98%) with an exon 19 EGFR deletion (n = 54, 52%). Forty-two patients (50%) had central nervous system (CNS) metastasis at the time of osimertinib initiation. ORR was 76%, median PFS and OS were 12.6 months and 52 months, respectively, and TTD was 33 months. At the time of analysis, 44 patients (42%) had tumor progression, and among these patients, 27 (61%) contributive samples were available. The most frequent molecular alterations at progression were mesenchymal epithelial transition factor (MET) amplification (15%; n = 4) and EGFR C797S mutation (11%; n = 3). Histological transformation was found in one patient (4%). RNA next-generation sequencing was performed in eight patients and showed a CCDC6-RET fusion in one patient (12%).

conclusionsWe confirmed the efficacy of osimertinib in patients with advanced EGFR mutation-positive NSCLC. At progression, the most frequent histomolecular alterations were MET amplification and EGFR C797S mutation.

Indexed as

Carcinoma, Non-Small-Cell LungDrug Resistance, NeoplasmLung NeoplasmsProtein Kinase InhibitorsAcrylamidesAniline CompoundsErbB ReceptorsHumansIndolesMutationPyrimidinesRetrospective StudiesAcrylamidesAniline CompoundsEGFR protein, humanErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidines

Identifiers

PMID36129569
OpenAlexW4297874882

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.