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  1. 3 Ιουν 2021 · In the OlympiA trial, we hypothesized that olaparib would provide benefit as an adjuvant therapy for patients with germline BRCA1 or BRCA2 pathogenic or likely pathogenic variant–associated ...

  2. 10 Οκτ 2022 · Adjuvant olaparib versus placebo significantly improved OS in g BRCA1 /2pv-associated human epidermal growth factor receptor 2-negative EBC (4-year OS 90% versus 86%). Adjuvant olaparib versus placebo improved 4-year IDFS (83% versus 75%) and 4-year DDFS (87% versus 79%).

  3. 1 Φεβ 2024 · OlympiA, a randomized, double-blind, parallel group, placebo (PL)-controlled, multi-center phase III study, compared 1 year of olaparib (OL) with PL as adjuvant therapy in patients with germline pathogenic or likely pathogenic variants in BRCA1 or BRCA2 (gBRCA1/2pv) and high-risk, human epidermal growth factor receptor 2 (HER2)–negative early ...

  4. Background: The randomized, double-blind OlympiA trial compared 1 year of the oral poly(adenosine diphosphate-ribose) polymerase inhibitor, olaparib, to matching placebo as adjuvant therapy for patients with pathogenic or likely pathogenic variants in germline BRCA1 or BRCA2 (gBRCA1/2pv) and high-risk, human epidermal growth factor receptor 2-ne...

  5. 12 Οκτ 2022 · With 3.5 years of median follow-up, OlympiA demonstrates statistically significant improvement in overall survival (OS) with adjuvant olaparib compared with placebo for patients with pathogenic or likely pathogenic variants in germline BRCA1 or BRCA2 and high-risk, HER2-negative early breast cancer. Adjuvant olaparib maintained improvements in ...

  6. 1 Δεκ 2022 · We now report the pre-specified second IA of OS with updates of IDFS, DDFS, and safety. One thousand eight hundred and thirty-six patients were randomly assigned to olaparib or placebo following (neo)adjuvant chemotherapy, surgery, and radiation therapy if indicated.

  7. 16 Ιουν 2021 · OlympiA: A phase III, multicenter, randomized, placebo-controlled trial of adjuvant olaparib after (neo)adjuvant chemotherapy in patients with germline BRCA1/2 mutations and high-risk HER2-negative early breast cancer. Authors: Andrew Tutt, Judy Ellen Garber, Bella Kaufman, Giuseppe Viale, Debora Fumagalli, Priya Rastogi, Richard D. Gelber, …

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