New England Journal of Medicine· 2016Q1· Klinik çalışma
Nivolumab ile Tekrarlayan Baş ve Boyun Skuamöz Hücreli Karsinom Tedavisi
Nivolumab for Recurrent Squamous-Cell Carcinoma of the Head and Neck
- 5.101atıf
- Q1SCImago
- 2016yıl
Kısa özet
Platin bazlı kemoterapi sonrası tekrarlayan baş ve boyun skuamöz hücreli karsinom hastalarında Nivolumab, PD-1'e karşı bir antikor olarak, genel sağkalımı anlamlı şekilde iyileştirerek yeni bir tedavi standardı sunmuştur.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- Nivolumab, platin tedavisine dirençli baş ve boyun kanserinde ortalama genel sağkalımı 2.4 ay uzatmıştır (7.5'e karşı 5.1 ay).
- Nivolumab ile 1 yıllık sağkalım oranı anlamlı derecede daha yüksekti (%36.0'a karşı %16.6).
- Nivolumab grubunda yanıt oranı daha yüksek (%13.3'e karşı %5.8) ve hastaların bildirdiği fonksiyonellik daha iyiydi.
- Nivolumab grubunda evre 3 veya 4 yan etkiler daha az görüldü (%13.1'e karşı %35.1).
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
BACKGROUND: Patients with recurrent or metastatic squamous-cell carcinoma of the head and neck after platinum chemotherapy have a very poor prognosis and limited therapeutic options. Nivolumab, an anti-programmed death 1 (PD-1) monoclonal antibody, was assessed as treatment for this condition. METHODS: In this randomized, open-label, phase 3 trial, we assigned, in a 2:1 ratio, 361 patients with recurrent squamous-cell carcinoma of the head and neck whose disease had progressed within 6 months after platinum-based chemotherapy to receive nivolumab (at a dose of 3 mg per kilogram of body weight) every 2 weeks or standard, single-agent systemic therapy (methotrexate, docetaxel, or cetuximab). The primary end point was overall survival. Additional end points included progression-free survival, rate of objective response, safety, and patient-reported quality of life. RESULTS: The median overall survival was 7.5 months (95% confidence interval [CI], 5.5 to 9.1) in the nivolumab group versus 5.1 months (95% CI, 4.0 to 6.0) in the group that received standard therapy. Overall survival was significantly longer with nivolumab than with standard therapy (hazard ratio for death, 0.70; 97.73% CI, 0.51 to 0.96; P=0.01), and the estimates of the 1-year survival rate were approximately 19 percentage points higher with nivolumab than with standard therapy (36.0% vs. 16.6%). The median progression-free survival was 2.0 months (95% CI, 1.9 to 2.1) with nivolumab versus 2.3 months (95% CI, 1.9 to 3.1) with standard therapy (hazard ratio for disease progression or death, 0.89; 95% CI, 0.70 to 1.13; P=0.32). The rate of progression-free survival at 6 months was 19.7% with nivolumab versus 9.9% with standard therapy. The response rate was 13.3% in the nivolumab group versus 5.8% in the standard-therapy group. Treatment-related adverse events of grade 3 or 4 occurred in 13.1% of the patients in the nivolumab group versus 35.1% of those in the standard-therapy group. Physical, role, and social functioning was stable in the nivolumab group, whereas it was meaningfully worse in the standard-therapy group. CONCLUSIONS: Among patients with platinum-refractory, recurrent squamous-cell carcinoma of the head and neck, treatment with nivolumab resulted in longer overall survival than treatment with standard, single-agent therapy. (Funded by Bristol-Myers Squibb; CheckMate 141 ClinicalTrials.gov number, NCT02105636 .).
Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2016 · DOI ↗
Ücretsiz hesapla devam et
Makaleye Sor ile bu makaleye günde 3 soru ücretsiz; makaleyi kaydet, kaynakçasını al, ilgi alanına göre her gün yeni özetler. Çıkarımlar Premium.
Web'de ücretsiz devam etGoogle ya da Apple hesabınla giriş; kart istemez. Bu makaleye geri dönersin.
Telefonda:
Alan: Kulak Burun Boğaz
OtorhinolaryngologyMedicine