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Osimertinib in patients with advanced/metastatic epidermal growth factor receptor T790M mutation-positive non-small
Benoît Colinet1, Jan P Van Meerbeeck2, Tine Cuppens3
1Department of Pneumology and Thoracic Oncology, Grand Hôpital de Charleroi, Gilly, Belgium.
Abstract:
Objectives: The aim of ASTRIS, a real-world study, was to assess the safety and efficacy of osimertinib in patients with locally advanced or metastatic (stage IIIB-IV) epidermal growth factor receptor (EGFR) T790M mutation-positive non-small cell lung cancer (NSCLC) who had received prior EGFR-tyrosine kinase inhibitor (TKI) therapy. Here, we describe the Belgian subset of the global ASTRIS study.Methods: Patients received osimertinib orally as one 80 mg tablet once daily until disease progression or unacceptable toxicity. Socio-demographic data, medical history, disease progression and survival status were collected and molecular testing for EGFR status was performed. Safety was also assessed. All collected data were summarized using descriptive statistics.Results: Of the 31 Belgian patients enrolled in the study, 9 (29.0%) discontinued treatment for disease progression and 5 (16.1%) due to other reasons. Among the 31 patients treated with osimertinib, 16 (51.6%, 95% CI 33.1-69.8) had a clinical response and 13 (41.9%) had stable disease as best response assessed by the investigator, with a disease control rate of 93.5%. The clinical response rate was 66.7% (6/9) in patients with brain/leptomeningeal metastases and 50.0% (4/8) in patients without brain/leptomeningeal metastases. About one third of the patients (11/31) reported at least one adverse event (AE) (35.5%) or serious AE (10/31; 32.3%) and 3/31 (9.7%) patients discontinued treatment due to AEs.Conclusion: We here demonstrate the effectiveness of osimertinib in a real-world setting in Belgian patients with locally advanced or metastatic T790M-positive NSCLC who had received previous EGFR-TKI treatment. No new safety signals were identified.
Insights
Osimertinib demonstrated effectiveness in Belgian patients with advanced EGFR T790M-positive non-small cell lung cancer (NSCLC) after prior treatment. The real-world study found a high disease control rate with manageable safety, confirming its efficacy in this population.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Non-small cell lung cancer (NSCLC) remains a leading cause of cancer mortality.
- Epidermal growth factor receptor (EGFR) mutations are key drivers in a subset of NSCLC.
- Acquired resistance to EGFR-tyrosine kinase inhibitors (TKIs) often involves the T790M mutation.
Purpose of the Study:
- To evaluate the real-world safety and efficacy of osimertinib in Belgian patients with locally advanced or metastatic EGFR T790M-positive NSCLC.
- To assess outcomes in patients previously treated with EGFR-TKIs.
- To describe the Belgian subset of the global ASTRIS study.
Main Methods:
- A real-world study involving 31 Belgian patients with locally advanced or metastatic EGFR T790M-positive NSCLC.
- Patients received daily oral osimertinib (80 mg) until disease progression or unacceptable toxicity.
- Data collection included socio-demographics, medical history, disease progression, survival, and safety assessments.
Main Results:
- A clinical response rate of 51.6% and a disease control rate of 93.5% were observed.
- The clinical response rate was higher in patients with brain/leptomeningeal metastases (66.7%) compared to those without (50.0%).
- Adverse events were reported in 35.5% of patients, with 9.7% discontinuing treatment due to AEs.
Conclusions:
- Osimertinib is effective in a real-world setting for Belgian patients with T790M-positive NSCLC who have received prior EGFR-TKI therapy.
- The safety profile of osimertinib in this population was consistent with previous findings, with no new safety signals identified.
- These findings support the use of osimertinib in routine clinical practice for eligible NSCLC patients.
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