Keynote-091 trial
Web24 jun. 2024 · KEYNOTE-091試験は、Stage IB~IIIAの切除後NSCLCに対する術後補助療法としてのペムブロリズマブの有用性を評価した無作為化第III相試験である。. 中間解析においてPD-L1の発現状態に関わらず無病生存期間(DFS)を有意に延長した一方、TPS≧50%集団では有意な差を ... WebKEYNOTE-091: A multicenter, randomized, triple-blind, placebo-controlled trial in patients with completely resected stage IB (T2a ≥4 cm), II, or IIIA NSCLC f Key Eligibility Criteria Completely resected stage IB (T2a ≥4 cm), II, or IIIA NSCLC per AJCC 7th ed, regardless of tumor PD-L1 expression
Keynote-091 trial
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Web6 dec. 2024 · KEYNOTE 564 is a phase III, placebo-controlled trial to assess pembrolizumab after surgery given on 3-week cycles for up to 17 cycles in patients with resected intermediate or high risk RCC with clear cell component (NCT03142334). This trial is expected to report in late 2024. Web10 jan. 2024 · IND.227/KEYNOTE-483 is a randomized, open-label, randomized Phase 2/3 trial (ClinicalTrials.gov, NCT02784171 ) sponsored and conducted by the Canadian Cancer Trials Group (CCTG) in collaboration ...
Web12 jul. 2024 · The KEYNOTE-091 trial investigated the effects of pembrolizumab compared to a placebo drug after standard adjuvant therapy. Results from both trials showed an overall positive effect of adjuvant therapy, specifically in disease-free progression. Prof. Webof the lung: APICAL trial. Transl Lung Cancer Res 2024;11:1606-18. 2. O'Brien M, Paz-Ares L, Marreaud S, et al. Pembrolizumab versus placebo as adjuvant therapy for completely resected stage IB-IIIA non-small-cell lung cancer (PEARLS/ KEYNOTE-091): an interim analysis of a randomised, triple-blind, phase 3 trial. Lancet Oncol 2024;23:1274-86. 3.
Web22 mrt. 2024 · Assuming the FDA approves Tecentriq in this setting, Roche might soon have competition. Keytruda's KEYNOTE-091 study is expected to deliver results sometime this year, and because it is used widely in metastatic disease as a first-line treatment, would likely be a preferred choice by many lung-cancer specialists, Welford wrote in a March … Web21 jul. 2015 · A Randomized, Phase 3 Trial With Anti-PD-1 Monoclonal Antibody Pembrolizumab (MK-3475) Versus Placebo for Patients With Early Stage NSCLC After Resection and Completion of Standard Adjuvant Therapy (PEARLS) Actual Study Start Date : November 6, 2015: Actual Primary Completion Date : January 24, 2024: Estimated …
Web10 jan. 2024 · NEW YORK – In Merck's Phase III Keynote-091 trial, adjuvant treatment with pembrolizumab (Keytruda) significantly improved disease-free survival over placebo in early-stage non-small cell lung cancer patients, regardless of PD-L1 expression status, the company said on Monday.
WebBackground: Pembrolizumab is a standard-of-care for advanced non-small-cell lung cancer (NSCLC). We assessed pembrolizumab as adjuvant therapy for completely resected stage IB-IIIA NSCLC. Methods: In this randomised, triple-blind, phase 3 trial (PEARLS/KEYNOTE-091), patients were recruited from 196 medical centres in 29 countries. unexpectedly yours summaryWeb13 apr. 2024 · Acceptance based on results from the Phase 3 KEYNOTE-859 trial, which showed significant overall survival benefit in these patients with HER2-negative disease, regardless of PD-L1 expression Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) has … thread breakingWeb2 jun. 2024 · Background: At the second interim analysis (IA2) of the triple-blind, phase 3 PEARLS/KEYNOTE-091 study (NCT02504372), pembrolizumab significantly improved DFS compared with placebo in patients (pts) with completely resected stage IB (T ≥4 cm) to IIIA NSCLC per AJCC v7, regardless of PD-L1 expression (N = 1177, HR 0.76, 95% CI 0.63 ... unexpected network error copying fileWeb26 jan. 2024 · Efficacy was evaluated in KEYNOTE-091 (NCT02504372), a multicenter, randomized, triple-blind, placebo-controlled trial. Patients had not received neoadjuvant radiotherapy or chemotherapy.... unexpected mutual weight gainWeb9001 Background: Pembro monotherapy showed durable antitumor activity as third-line or later therapy for metastatic SCLC, leading to FDA approval in that setting. KEYNOTE-604 was a double-blind, phase 3 study of pembro + EP vs placebo + EP as first-line therapy for ES-SCLC (NCT03066778). Methods: Eligible patients (pts) with previously untreated ES … unexpectedly surprisedWeb27 jan. 2024 · Approval based on KEYNOTE-091 trial, which demonstrated a clinically meaningful improvement in disease-free survival with KEYTRUDA in these patients following surgical resection and platinum-based chemotherapy versus placebo Approval marks fifth indication for KEYTRUDA-based regimens in NSCLC and 34th indication for KEYTRUDA … thread breaks when sewingWeb18 mrt. 2024 · Study Details Investigators in the multinational PEARLS/KEYNOTE-091 trial enrolled patients with stage Ib-IIIa NSCLC and negative margins after surgical resection. After centralized assessment of... unexpected message author