Journals / Journal of Clinical and Analytical Medicine / 2015 / Cilt: 6 - Sayı: 2

Küçük Hücreli Dışı Akciğer Kanserli Hastalarda Erlotinibin Klinik Etkinliğinin Retrospektif Analizi

Retrospective Analysis of Clinical Efficacy of Erlotinib in Patients with Non-Small Cell Lung Cancer

Pages
212–215
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The median progression-free survival was 242 days (95% CI51-224), and the median overall survival (OS) was 377 days (95% CI 291- 462).

📌 3 Key Takeaways

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Objective & Hypothesis:Aim: In this study, we aimed to evaluate the efficacy and safety of erlotinib assecond-, third-, and fourth-line treatment for Turkish patients with advancednon-small cell lung cancer (NSCLC).
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Key Findings & Data:Material and Method: Thirty-nine patients with advanced, previously treated NSCLC who received 150 mg of erlotinib once daily orally until disease progression or intolerable toxicity wereretrospectively analyzed.
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Conclusion & Impact:The median progression-free survival was 242 days (95% CI51-224), and the median overall survival (OS) was 377 days (95% CI 291- 462).
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Aim: In this study, we aimed to evaluate the efficacy and safety of erlotinib assecond-, third-, and fourth-line treatment for Turkish patients with advancednon-small cell lung cancer (NSCLC). Material and Method: Thirty-nine patients with advanced, previously treated NSCLC who received 150 mg of erlotinib once daily orally until disease progression or intolerable toxicity wereretrospectively analyzed. Results: We observed no complete response, partialresponses were observed in 7 (17.9%) patients, and 16 (41%) patients hadstable disease. The median progression-free survival was 242 days (95% CI51-224), and the median overall survival (OS) was 377 days (95% CI 291- 462). The median OS of females was significantly better than male patients(470 vs. 271 days, p=0.046). The treatment was generally well tolerated. Themost common side effect was skin rash (41%). Discussion: Erlotinib was safeand effective in treating Turkish patients with advanced NSCLC who hadbeen previously treated with the standard chemotherapy.

Özet

Amaç: Bu çalışmada, ileri evre küçük hücreli dışı akciğer kanseri (KHDAK) olanTürk hastalarda, ikinci, üçüncü ve dördüncü seçim olarak uygulanan erlotinibin etkinlik ve güvenilirliğinin değerlendirilmesi amaçlandı. Gereç ve Yöntem:Daha önce tedavi görmüş, ileri evre KHDAK olan ve hastalık progresyonuna veya tolere edilemeyen bir yan etki oluşana kadar, oral yoldan günde 150mg erlotinib alan 39 hasta retrospektif olarak analiz edildi. Bulgular: Tam yanıt gözlenmezken, 7 (%17.9) hastada kısmi yanıt ve 16 (%41) hastada stabil hastalık tespit edildi. Ortalama progresyonsuz sağkalım süresi 242 gün(%95 CI 51-224) ve ortalama genel sağkalım süresi ise 377 gündü (%95 CI291-462). Genel sağkalım süresi kadınlarda erkeklere oranla anlamlı düzeydedaha uzundu (470 vs. 271 gün, p=0.046). Tedavi genel olarak iyi tolere edildi. En sık gözlenen yan etki cilt döküntüsü idi (%41). Tartışma: Erlotinib dahaönce standart kemoterapi almış ileri evre KHDAK olan Türk hastaların tedavisinde güvelinilir ve etkili bulundu.

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Cite This Article

DELİGÖNÜL, A., KANAT, Ö., AYYILDIZ, A., GÜRSOY, V., ÖZKAYA, G. (2022). Küçük Hücreli Dışı Akciğer Kanserli Hastalarda Erlotinibin Klinik Etkinliğinin Retrospektif Analizi. Journal of Clinical and Analytical Medicine, Cilt: 6 - Sayı: 2, 212–215. https://ajindex.com/articles/553917

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