Real World Data on the Efficacy of Brigatinib in ALK-Positive Non-Small Cell Lung Cancer: A Single-Center Experience
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2025
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| author | Ćeriman Krstić, Vesna Samardžić, Natalija Stjepanović, Mihailo Popević, Spasoje Adžić- Vukičević, Tatjana Glumac, Sofija Stević, Ruža Marić, Dragana Velinović, Marta Jovanović, Milena Ilić, Branislav Gajić, Milija Čolić, Nikola Lukić, Katarina Milošević Maračić, Brankica Stamenić, Slavko Sekulović Radovanović, Ivana Milin Lazović, Jelena |
| author_facet | Ćeriman Krstić, Vesna Samardžić, Natalija Stjepanović, Mihailo Popević, Spasoje Adžić- Vukičević, Tatjana Glumac, Sofija Stević, Ruža Marić, Dragana Velinović, Marta Jovanović, Milena Ilić, Branislav Gajić, Milija Čolić, Nikola Lukić, Katarina Milošević Maračić, Brankica Stamenić, Slavko Sekulović Radovanović, Ivana Milin Lazović, Jelena |
| contents | <div> <h3>Abstract</h3> </div> <div> <p><span>Introduction: Lung cancer remains the leading cause of cancer death among all cancers. The discovery of epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) mutations led to an increased survival rate in patients with locally advanced and metastatic non-small cell lung cancer (NSCLC). Results of the ALTA 1L study showed superior outcomes for patients treated with brigatinib compared to patients treated with crizotinib. Background: We conducted research including 23 patients with ALK-positive lung adenocarcinoma who were treated with brigatinib in first or further lines of therapy. The median follow-up was 22 months (4–66 months). Results: There were no significant differences in patient population between the first and further lines of treatment regarding sex distribution (p = 0.692), smoking status (p = 0.554), ECOG performance status (p = 1.000), and baseline presence of brain metastases (p = 0.862). The response rate was 47.8%, and disease control was 95.6%. The 12-month progression-free survival (PFS) and overall survival (OS) rates were 85.3% and 86.5%, respectively, while the 60-month PFS rate was not reached, and the 60-month OS rate was 27.1%. The mPFS and mOS were 32 months. Conclusions: The results of this analysis are promising, as our patients experienced better outcomes compared to those in the ALTA 1L study, which may be attributed to the small sample size. However, the effectiveness of brigatinib has been confirmed in our clinical practice.</span></p> </div> |
| format | Recurso digital |
| id | zenodo_https___doi_org_10_3390_cancers17183084 |
| institution | Zenodo |
| language | eng |
| publishDate | 2025 |
| publisher | Zenodo |
| record_format | zenodo |
| spellingShingle | Real World Data on the Efficacy of Brigatinib in ALK-Positive Non-Small Cell Lung Cancer: A Single-Center Experience Ćeriman Krstić, Vesna Samardžić, Natalija Stjepanović, Mihailo Popević, Spasoje Adžić- Vukičević, Tatjana Glumac, Sofija Stević, Ruža Marić, Dragana Velinović, Marta Jovanović, Milena Ilić, Branislav Gajić, Milija Čolić, Nikola Lukić, Katarina Milošević Maračić, Brankica Stamenić, Slavko Sekulović Radovanović, Ivana Milin Lazović, Jelena ALK-positive brigatinib NSCLC OS PFS <div> <h3>Abstract</h3> </div> <div> <p><span>Introduction: Lung cancer remains the leading cause of cancer death among all cancers. The discovery of epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) mutations led to an increased survival rate in patients with locally advanced and metastatic non-small cell lung cancer (NSCLC). Results of the ALTA 1L study showed superior outcomes for patients treated with brigatinib compared to patients treated with crizotinib. Background: We conducted research including 23 patients with ALK-positive lung adenocarcinoma who were treated with brigatinib in first or further lines of therapy. The median follow-up was 22 months (4–66 months). Results: There were no significant differences in patient population between the first and further lines of treatment regarding sex distribution (p = 0.692), smoking status (p = 0.554), ECOG performance status (p = 1.000), and baseline presence of brain metastases (p = 0.862). The response rate was 47.8%, and disease control was 95.6%. The 12-month progression-free survival (PFS) and overall survival (OS) rates were 85.3% and 86.5%, respectively, while the 60-month PFS rate was not reached, and the 60-month OS rate was 27.1%. The mPFS and mOS were 32 months. Conclusions: The results of this analysis are promising, as our patients experienced better outcomes compared to those in the ALTA 1L study, which may be attributed to the small sample size. However, the effectiveness of brigatinib has been confirmed in our clinical practice.</span></p> </div> |
| title | Real World Data on the Efficacy of Brigatinib in ALK-Positive Non-Small Cell Lung Cancer: A Single-Center Experience |
| topic | ALK-positive brigatinib NSCLC OS PFS |
| url | https://doi.org/10.3390/cancers17183084 |