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Updated: Feb 11, 2026

Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
Abstract:
Findings from a phase I study indicate that the investigational RET inhibitor BLU-667 is safe and well tolerated, inducing good responses in patients with RET-altered medullary thyroid cancer or non-small cell lung cancer.
Insights
The investigational drug BLU-667 shows promise as a safe treatment for patients with RET-altered thyroid and lung cancers. Early study results reveal good patient responses, indicating its potential therapeutic value.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Medullary thyroid cancer (MTC) and non-small cell lung cancer (NSCLC) often harbor RET alterations.
- Targeted therapies are crucial for improving outcomes in these challenging malignancies.
- RET proto-oncogene alterations represent a key driver in a subset of MTC and NSCLC cases.
Discussion:
- BLU-667, a novel RET inhibitor, was evaluated in a Phase I clinical trial.
- The study assessed safety, tolerability, and preliminary efficacy of BLU-667.
- Pharmacokinetic and pharmacodynamic assessments provided insights into drug behavior.
Key Insights:
- BLU-667 demonstrated a favorable safety and tolerability profile in patients.
- The investigational agent induced notable responses in patients with RET-altered MTC and NSCLC.
- These findings support further clinical development of BLU-667 for RET-driven cancers.
Outlook:
- Further clinical trials are warranted to confirm efficacy and optimize dosing.
- BLU-667 holds potential as a new targeted therapy option.
- Continued research will explore its role in various RET-altered malignancies.
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