New England Journal of Medicine· 2019Q1
EGFR Mutasyonlu İleri Evre Küçük Hücreli Dışı Akciğer Kanseri Hastalarında Osimertinib ile Genel Sağkalım
Overall Survival with Osimertinib in Untreated, <i>EGFR</i> -Mutated Advanced NSCLC
- 2.846atıf
- Q1SCImago
- 2019yıl
Kısa özet
Tedavi edilmemiş, EGFR mutasyonlu ileri evre küçük hücreli dışı akciğer kanseri (KHDAK) hastalarında, diğer EGFR-TKI'lara kıyasla ilk basamak osimertinib tedavisi genel sağkalımı anlamlı şekilde 6.8 ay iyileştirmiştir (38.6'ya karşılık 31.8 ay).
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- İlk basamak osimertinib, karşılaştırıcı EGFR-TKI'lara göre 38.6 ay medyan genel sağkalım ile sonuçlanmıştır (31.8 ay).
- Osimertinib ile ölüm için tehlike oranı 0.80'dir (95.05% GÜ, 0.64 ila 1.00; P = 0.046).
- 3 yılın sonunda, osimertinib alan hastaların %28'i tedaviye devam ederken, karşılaştırıcı TKI alanlarda bu oran %9'du.
- 3. derece veya daha yüksek yan etkiler, osimertinib grubundaki hastaların %42'sinde ve karşılaştırıcı gruptakilerin %47'sinde bildirilmiştir.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
BACKGROUND: Osimertinib is a third-generation, irreversible tyrosine kinase inhibitor of the epidermal growth factor receptor (EGFR-TKI) that selectively inhibits both EGFR-TKI-sensitizing and EGFR T790M resistance mutations. A phase 3 trial compared first-line osimertinib with other EGFR-TKIs in patients with EGFR mutation-positive advanced non-small-cell lung cancer (NSCLC). The trial showed longer progression-free survival with osimertinib than with the comparator EGFR-TKIs (hazard ratio for disease progression or death, 0.46). Data from the final analysis of overall survival have not been reported. METHODS: In this trial, we randomly assigned 556 patients with previously untreated advanced NSCLC with an EGFR mutation (exon 19 deletion or L858R allele) in a 1:1 ratio to receive either osimertinib (80 mg once daily) or one of two other EGFR-TKIs (gefitinib at a dose of 250 mg once daily or erlotinib at a dose of 150 mg once daily, with patients receiving these drugs combined in a single comparator group). Overall survival was a secondary end point. RESULTS: The median overall survival was 38.6 months (95% confidence interval [CI], 34.5 to 41.8) in the osimertinib group and 31.8 months (95% CI, 26.6 to 36.0) in the comparator group (hazard ratio for death, 0.80; 95.05% CI, 0.64 to 1.00; P = 0.046). At 3 years, 79 of 279 patients (28%) in the osimertinib group and 26 of 277 (9%) in the comparator group were continuing to receive a trial regimen; the median exposure was 20.7 months and 11.5 months, respectively. Adverse events of grade 3 or higher were reported in 42% of the patients in the osimertinib group and in 47% of those in the comparator group. CONCLUSIONS: Among patients with previously untreated advanced NSCLC with an EGFR mutation, those who received osimertinib had longer overall survival than those who received a comparator EGFR-TKI. The safety profile for osimertinib was similar to that of the comparator EGFR-TKIs, despite a longer duration of exposure in the osimertinib group. (Funded by AstraZeneca; FLAURA ClinicalTrials.gov number, NCT02296125.).
Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2019 · DOI ↗
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