Amivantamab as a salvage therapy post-EGFR-tyrosine kinase inhibitor failure in patients with mutated EGFR non-small cell lung cancer

This pilot study suggests that adding late-line amivantamab to an ongoing EGFR-TKI may have potential benefits in selected non-small cell lung cancer (NSCLC) patients with EGFR mutations, but resulted in high skin toxicity. Patients with EGFR L858R mutations appeared to show improved responses to amivantamab compared to the lack of response with ex19dels, while acquired resistance was associated with loss of the original EGFR driver mutation and MET alterations. However, these preliminary findings lack robust evidence due to study limitations, and larger, prospective, multi-center trials are needed to validate these results.

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Publication Details

Journal
Translational Lung Cancer Research
Published
2025-03-01
DOI
https://doi.org/10.21037/tlcr-24-617
Primary Topic
Lung Cancer Treatments and Mutations
Type
article
Field-Weighted Citation Impact
0.00
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article

Amivantamab as a salvage therapy post-EGFR-tyrosine kinase inhibitor failure in patients with mutated EGFR non-small cell lung cancer

Laila C. Roisman, Areen Abu Remilah, Inbal Granot, Gleb Kornev et al.
Translational Lung Cancer Research
Lung Cancer Treatments and Mutations
article

Amivantamab as a salvage therapy post-EGFR-tyrosine kinase inhibitor failure in patients with mutated EGFR non-small cell lung cancer

Laila C. Roisman, Areen Abu Remilah, Inbal Granot, Gleb Kornev, Naama Bogot, Bilal Krayim, Nir Peled, Noam Asna, Waleed Kian, D. Kahala, Julia Dudnik, Michal Nissim, Maria Spector
article en

Abstract

This pilot study suggests that adding late-line amivantamab to an ongoing EGFR-TKI may have potential benefits in selected non-small cell lung cancer (NSCLC) patients with EGFR mutations, but resulted in high skin toxicity. Patients with EGFR L858R mutations appeared to show improved responses to amivantamab compared to the lack of response with ex19dels, while acquired resistance was associated with loss of the original EGFR driver mutation and MET alterations. However, these preliminary findings lack robust evidence due to study limitations, and larger, prospective, multi-center trials are needed to validate these results.

Translational Lung Cancer ResearchVol. 14(3)
Ben-Gurion University of the Negev (IL), Soroka Medical Center (IL)
Openalex Percentile: Top 92%
Lung Cancer Treatments and Mutations
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