Paper Details 
Original Abstract of the Article :
<b>Aim:</b> To assess time-to-treatment discontinuation (TTD) of brigatinib following treatment with ALK tyrosine kinase inhibitor(s) (TKIs) in patients with ALK-positive (ALK+) non-small-cell lung cancer (NSCLC) receiving brigatinib through the international early access program. <b>Patients &amp;...See full text at original site
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引用元:
https://doi.org/10.2217/fon-2019-0849

データ提供:米国国立医学図書館(NLM)

Brigatinib: A Beacon of Hope in the Treatment of ALK-Positive Lung Cancer

ALK-positive non-small-cell lung cancer (NSCLC), a particularly aggressive form of lung cancer, presents significant challenges for oncologists. This study examines the real-world effectiveness and tolerability of brigatinib, a novel ALK tyrosine kinase inhibitor (TKI), in patients with ALK+ NSCLC.

Brigatinib: A Promising Treatment for ALK-Positive Lung Cancer

The researchers analyzed data from patients with ALK+ NSCLC who received brigatinib through an early access program. Their findings indicate that brigatinib demonstrated clinical efficacy and tolerability, even in patients who had previously received other ALK TKIs, highlighting its potential as a valuable treatment option for ALK+ NSCLC.

The Promise of Brigatinib in the Fight Against Lung Cancer

This study provides encouraging real-world evidence supporting the efficacy of brigatinib in treating ALK+ NSCLC. These findings underscore the importance of continued research and development of novel therapies to improve the lives of patients battling this challenging disease.

Dr. Camel's Conclusion

Lung cancer, like a relentless desert storm, can be a formidable adversary. This study, like a guiding oasis in the vast expanse of cancer research, sheds light on the promise of brigatinib as a treatment for ALK-positive lung cancer. These findings offer a glimmer of hope in the fight against this devastating disease, reminding us that the pursuit of effective therapies is a journey worth undertaking.

Date :
  1. Date Completed 2021-02-08
  2. Date Revised 2021-02-08
Further Info :

Pubmed ID

32338548

DOI: Digital Object Identifier

10.2217/fon-2019-0849

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English

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