(Lung Cancer) Is Keytruda Effective?
Medical Supporter — إشعار معلوماتي
هذه المقالة ملخص لمعلومات طبية دولية وليست نصيحة طبية، ولا يمكن أن تحل محل تشخيص طبيبك المعالج أو خطة العلاج. المعلومات المعروضة مجمّعة من منشورات عامة وبيانات رسمية لكبرى المؤسسات الطبية اليابانية؛ وتختلف ملاءمة ونتائج أي علاج من مريض لآخر ويجب أن يقيّمها طبيب مؤهل لكل حالة على حدة.
On June 3, 2023, Heather Wakelee et al. from Stanford University published the results of the Phase 3 KEYNOTE-671 clinical trial in "The New England Journal of Medicine," evaluating the efficacy and safety of Keytruda as perioperative (pre- and post-operative) chemotherapy for patients with early-stage non-small cell lung cancer (NSCLC).
This trial randomly assigned patients with stage II-IIIB NSCLC in a 1:1 ratio to either the Keytruda group (pre-operative pembrolizumab with chemotherapy followed by post-operative pembrolizumab monotherapy) or the placebo group. The primary endpoints were event-free survival (EFS) and overall survival (OS). Secondary endpoints included major pathological response (mPR), pathological complete response (pCR), and safety.
At a median follow-up of 25.2 months, the 24-month event-free survival rates (a primary endpoint) were 62.4% for the Keytruda group and 40.6% for the placebo group. The 24-month overall survival rates (another primary endpoint) were 80.9% for the Keytruda group and 77.6% for the placebo group.
For secondary endpoints, the major pathological response rates were 30.2% in the Keytruda group and 11.0% in the placebo group. The pathological complete response rates were 18.1% in the Keytruda group and 4.0% in the placebo group.
In terms of safety, the incidence of grade 3 or higher adverse events was 44.9% in the Keytruda group and 37.3% in the placebo group. The incidence of grade 5 or higher adverse events was 1.0% in the Keytruda group and 0.8% in the placebo group.
Based on the results of the KEYNOTE-671 trial, Heather Wakelee et al. stated that the use of Keytruda as perioperative chemotherapy in patients with early-stage NSCLC significantly improved event-free survival, major pathological response, and pathological complete response compared to the placebo group. However, no significant difference in overall survival was confirmed in this analysis.
Source: https://www.nejm.org/doi/full/10.1056/NEJMoa2302983?query=featured_home?query=featured_home
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هل تفكر في تلقّي العلاج في اليابان؟ هل تحتاج إلى معلومات ومساعدة؟
نساعدك في تنظيم المعلومات اللازمة للسفر الطبي إلى اليابان، والتواصل مع المؤسسات الطبية اليابانية، وترتيب استشارة رأي ثانٍ.الاستشارة الأولى مجانية؛ سيساعدك المستشار على توضيح الخطوات التالية.
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