# Lorlatinib and Amivantamab: A Paradigm Shift in EGFR and ALK Positive NSCLC, with More Effective but More Toxic Treatments Requiring a Well-Structured Shared Decision Making

**Authors:** Paolo Maione, Valentina Palma, Cesare Gridelli

PMC · DOI: 10.32604/or.2026.072992 · Oncology Research · 2026-03-23

## TL;DR

New treatments for EGFR and ALK positive lung cancer offer better survival but come with significant new side effects requiring careful patient discussions.

## Contribution

Highlights the need for structured shared decision-making due to the unique toxicity profiles of new EGFR and ALK therapies.

## Key findings

- Amivantamab plus lazertinib and lorlatinib show improved efficacy in EGFR and ALK positive NSCLC.
- These treatments introduce new safety concerns that impact patients' quality of life.
- Shared decision-making is essential to balance survival benefits and toxicity risks with patients.

## Abstract

After about 20 years of exciting improvements in treatment efficacy outcomes of advanced epidermal growth factor receptor (EGFR) mutant and anaplastic lymphoma kinase (ALK) rearranged non-small cell lung cancer (NSCLC), also combined with a progressively better safety profile, from chemotherapy to new generation tyrosine kinase inhibitors (TKIs) (osimertinib, alectinib, brigatinib), the recent MARIPOSA and CROWN trials have changed this trend. For the first time in the history of EGFR and ALK treatments, we must face the issue of being a step behind in terms of toxicity profile. The combination of amivantamab plus lazertinib in EGFR mutant NSCLC, and lorlatinib in ALK rearranged NSCLC, has improved efficacy outcomes as never before. The story would be easy and totally positive if these two innovative, amazing treatments were not associated with new peculiar features in safety profiles that must be discussed with patients, because they potentially affect their quality of life. When treating these patient populations, the peculiar safety profiles of amivantamab plu lazertinib and lorlatinib require a well-structured shared decision making, “where and when”, both the high probability of a longer survival and the risk of worse quality of life must be well announced and explained to our patients before the shared final treatment choice.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956], ALK (ALK receptor tyrosine kinase) [NCBI Gene 238]
- **Chemicals:** lorlatinib (PubChem CID 71731823), lazertinib (PubChem CID 121269225), osimertinib (PubChem CID 71496458), alectinib (PubChem CID 49806720), brigatinib (PubChem CID 68165256)
- **Diseases:** non-small cell lung cancer (MONDO:0005233), NSCLC (MONDO:0005233)

## Full-text entities

- **Genes:** ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** toxicity (MESH:D064420), NSCLC (MESH:D002289)
- **Chemicals:** alectinib (MESH:C582670), osimertinib (MESH:C000596361), Amivantamab (MESH:C000718215), tyrosine (MESH:D014443), lazertinib (MESH:C000707992), Lorlatinib (MESH:C000590786), brigatinib (MESH:C000598580)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13040341/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC13040341/full.md

---
Source: https://tomesphere.com/paper/PMC13040341