Evidence map›Paper›PMID 37856922›Full record

ArticleLung cancer (Amsterdam, Netherlands)2023

Durable response to amivantamab in treatment refractory NSCLC harboring EGFR and complex MET mutations: A case report.

Lauren Schmalz, Chance Bloomer, Wei Zhang, William Petty

Open access · greenAbstract readCase Reports
In one paragraph

Article in Lung cancer (Amsterdam, Netherlands), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Lauren SchmalzDepartment of Hematology/Oncology, Wake Forest University School of Medicine, 1 Medical Center Blvd, Winston-Salem, NC 27157, United States. Electronic address: lschmalz@wakehealth.edu.
Chance BloomerDepartment of Internal Medicine, Wake Forest University School of Medicine, 1 Medical Center Blvd, Winston-Salem, NC 27157, United States.
Wei ZhangWake Forest Baptist Comprehensive Cancer Center, 1 Medical Center Blvd, Winston-Salem, NC 27157, United States.
William PettyWake Forest Baptist Comprehensive Cancer Center, 1 Medical Center Blvd, Winston-Salem, NC 27157, United States.
Wake Forest Baptist Comprehensive Cancer CenterWake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Translational Oncology Training ProgramT32CA247819 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARDEE, TIMOTHY SEBASTIAN, WATABE, KOUNOSUKE · 2020 to 2024
$1.4M
NCI NIH HHS P30 CA012197NCI NIH HHS T32 CA247819
6 · The paper itself

Abstract

Targeted therapies have revolutionized treatment for metastatic non-small cell lung cancer (NSCLC) with oncogenic driver mutations. However, challenges arise in managing concurrent mutations and overcoming resistance. We present the case of a patient with epidermal growth factor receptor (EGFR) (L747_A750delinsP exon19 deletion) and mesenchymal-epithelial transition factor (MET) mutations (D1228H, D1228N, D1228Y, Y1230H, MET amplification) who achieved a durable response to amivantamab (14 months ongoing) after progression on multiple lines of therapy including platinum-based chemotherapy, EGFR tyrosine kinase inhibitors (TKI) and combination TKI and MET inhibitors. This case highlights the utility of longitudinal next-generation sequencing (NGS) testing to identify acquired resistance and the need for continued research into understanding mechanisms of resistance to help develop future treatment strategies.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntibodies, BispecificDrug Resistance, NeoplasmErbB ReceptorsHumansMutationProtein Kinase InhibitorsamivantamabAntibodies, BispecificEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsAmivantamabEGFR mutationMET mutationNon-small cell lung cancer

Identifiers

PMID37856922
PMCPMC10842023
OpenAlexW4387521234

What OpenQuestion holds

Textmetadata
LicenceTDM
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.