New England Journal of Medicine· 2017Q1
Kronik Miyeloid Lösemi Tedavisinde İmatinib'in Uzun Dönem Sonuçları
Long-Term Outcomes of Imatinib Treatment for Chronic Myeloid Leukemia
- 1.267atıf
- Q1SCImago
- 2017yıl
Kısa özet
Yaklaşık 11 yıllık takip sonucunda, kronik miyeloid lösemi (KML) tedavisinde imatinib, %83,3'lük genel sağkalım oranı ile kalıcı etkinlik ve kabul edilebilir bir güvenlik profili sergiledi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- İmatinib ile tedavi edilen KML hastalarında 10 yıllık tahmini genel sağkalım oranı %83,3 olarak belirlendi.
- İmatinib'e rastgele atanan hastaların %82,8'i tam sitogenetik yanıt elde etti.
- İmatinib ile ilişkili ciddi yan etkiler seyrek görüldü ve öncelikle ilk yıl içinde ortaya çıktı.
- İmatinib'in uzun süreli uygulanması, kabul edilemez kümülatif veya geç toksik etkilerle ilişkilendirilmedi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
BACKGROUND: Imatinib, a selective BCR-ABL1 kinase inhibitor, improved the prognosis for patients with chronic myeloid leukemia (CML). We conducted efficacy and safety analyses on the basis of more than 10 years of follow-up in patients with CML who were treated with imatinib as initial therapy. METHODS: In this open-label, multicenter trial with crossover design, we randomly assigned patients with newly diagnosed CML in the chronic phase to receive either imatinib or interferon alfa plus cytarabine. Long-term analyses included overall survival, response to treatment, and serious adverse events. RESULTS: The median follow-up was 10.9 years. Given the high rate of crossover among patients who had been randomly assigned to receive interferon alfa plus cytarabine (65.6%) and the short duration of therapy before crossover in these patients (median, 0.8 years), the current analyses focused on patients who had been randomly assigned to receive imatinib. Among the patients in the imatinib group, the estimated overall survival rate at 10 years was 83.3%. Approximately half the patients (48.3%) who had been randomly assigned to imatinib completed study treatment with imatinib, and 82.8% had a complete cytogenetic response. Serious adverse events that were considered by the investigators to be related to imatinib were uncommon and most frequently occurred during the first year of treatment. CONCLUSIONS: Almost 11 years of follow-up showed that the efficacy of imatinib persisted over time and that long-term administration of imatinib was not associated with unacceptable cumulative or late toxic effects. (Funded by Novartis Pharmaceuticals; IRIS ClinicalTrials.gov numbers, NCT00006343 and NCT00333840 .).
Yazarların özeti; kaynağından alınmıştır. New England Journal of Medicine, 2017 · DOI ↗
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Alan: Hematoloji
HematologyMedicine