50 research outputs found

    Cemiplimab in locally advanced or metastatic cutaneous squamous cell carcinoma:prospective real-world data from the DRUG Access Protocol

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    Background: The DRUG Access Protocol provides patients with cancer access to registered anti-cancer drugs that are awaiting reimbursement in the Netherlands and simultaneously collects prospective real-world data (RWD). Here, we present RWD from PD-1 blocker cemiplimab in patients with locally advanced or metastatic cutaneous squamous cell carcinoma (laCSCC; mCSCC). Methods: Patients with laCSCC or mCSCC received cemiplimab 350 mg fixed dose every three weeks. Primary endpoints were objective clinical benefit rate (CBR), defined as objective response (OR) or stable disease (SD) at 16 weeks, physician-assessed CBR, defined as clinician's documentation of improved disease or SD based on evaluation of all available clinical parameters at 16 weeks, objective response rate (ORR), and safety, defined as grade ≥ 3 treatment related adverse events (TRAEs) occurring up to 30 days after last drug administration. Secondary endpoints included duration of response (DoR), progression-free survival (PFS), and overall survival (OS). Findings: Between February 2021 and December 2022, 151 patients started treatment. Objective and physician-assessed CBR were 54.3% (95% CI, 46.0–62.4) and 59.6% (95% CI, 51.3–67.5), respectively. ORR was 35.1% (95% CI, 27.5–43.3). After a median follow-up of 15.2 months, median DoR was not reached. Median PFS and OS were 12.2 (95% CI, 7.0-not reached) and 24.2 months (95% CI, 18.8-not reached), respectively. Sixty-eight TRAEs occurred in 29.8% of patients. Most commonly reported TRAE was a kidney transplant rejection (9.5%). Interpretation: Cemiplimab proved highly effective and safe in this real-world cohort of patients with laCSCC or mCSCC, confirming its therapeutic value in the treatment of advanced CSCC in daily clinical practice. Funding: The DRUG Access Protocol is supported by all participating pharmaceutical companies: Bayer, Janssen, Lilly, Merck, Novartis, Roche, and Sanofi.</p

    Cemiplimab in locally advanced or metastatic cutaneous squamous cell carcinoma:prospective real-world data from the DRUG Access Protocol

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    Background: The DRUG Access Protocol provides patients with cancer access to registered anti-cancer drugs that are awaiting reimbursement in the Netherlands and simultaneously collects prospective real-world data (RWD). Here, we present RWD from PD-1 blocker cemiplimab in patients with locally advanced or metastatic cutaneous squamous cell carcinoma (laCSCC; mCSCC). Methods: Patients with laCSCC or mCSCC received cemiplimab 350 mg fixed dose every three weeks. Primary endpoints were objective clinical benefit rate (CBR), defined as objective response (OR) or stable disease (SD) at 16 weeks, physician-assessed CBR, defined as clinician's documentation of improved disease or SD based on evaluation of all available clinical parameters at 16 weeks, objective response rate (ORR), and safety, defined as grade ≥ 3 treatment related adverse events (TRAEs) occurring up to 30 days after last drug administration. Secondary endpoints included duration of response (DoR), progression-free survival (PFS), and overall survival (OS). Findings: Between February 2021 and December 2022, 151 patients started treatment. Objective and physician-assessed CBR were 54.3% (95% CI, 46.0–62.4) and 59.6% (95% CI, 51.3–67.5), respectively. ORR was 35.1% (95% CI, 27.5–43.3). After a median follow-up of 15.2 months, median DoR was not reached. Median PFS and OS were 12.2 (95% CI, 7.0-not reached) and 24.2 months (95% CI, 18.8-not reached), respectively. Sixty-eight TRAEs occurred in 29.8% of patients. Most commonly reported TRAE was a kidney transplant rejection (9.5%). Interpretation: Cemiplimab proved highly effective and safe in this real-world cohort of patients with laCSCC or mCSCC, confirming its therapeutic value in the treatment of advanced CSCC in daily clinical practice. Funding: The DRUG Access Protocol is supported by all participating pharmaceutical companies: Bayer, Janssen, Lilly, Merck, Novartis, Roche, and Sanofi.</p

    The James Webb Space Telescope Mission

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    Twenty-six years ago a small committee report, building on earlier studies, expounded a compelling and poetic vision for the future of astronomy, calling for an infrared-optimized space telescope with an aperture of at least 4m4m. With the support of their governments in the US, Europe, and Canada, 20,000 people realized that vision as the 6.5m6.5m James Webb Space Telescope. A generation of astronomers will celebrate their accomplishments for the life of the mission, potentially as long as 20 years, and beyond. This report and the scientific discoveries that follow are extended thank-you notes to the 20,000 team members. The telescope is working perfectly, with much better image quality than expected. In this and accompanying papers, we give a brief history, describe the observatory, outline its objectives and current observing program, and discuss the inventions and people who made it possible. We cite detailed reports on the design and the measured performance on orbit.Comment: Accepted by PASP for the special issue on The James Webb Space Telescope Overview, 29 pages, 4 figure

    Suivi prospectif des malformations bronchopulmonaires de diagnostic prénatal au CHU de Rennes de 2006 à 2008

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    RENNES1-BU Santé (352382103) / SudocPARIS-BIUM (751062103) / SudocSudocFranceF

    BILAN ET INTERET DE L'IMAGERIE DANS LES LUXATIONS CONGENITALES IRREDUCTIBLES DE LA HANCHE NEONATALE

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    RENNES1-BU Santé (352382103) / SudocPARIS-BIUM (751062103) / SudocSudocFranceF

    Soil variations in northern French Guiana that could modify forest dynamics

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    International audienceDes facteurs du milieu tels que le sol et la topographie influencent la productivité et la biomasse de la forêt tropicale humide. Extrapoler à l'échelle d'un pays les données de biomasse qui sont disponibles à une échelle locale demande donc de connaître l'organisation des sols à l'échelle d'un pays. En Guyane française, cette organisation des sols est très bien connue à une échelle locale avec le type de drainage comme principal facteur de différenciation des sols. Mais elle est moins connue à l'échelle plus large de la Guyane. Les objectifs de cette étude sont de donner un premier aperçu de l'organisation des sols forestiers du nord de la Guyane ainsi que de leur niveau de fertilité chimique en tenant compte de la pluviosité annuelle (2000 à 4000 mm), la géologie (quatre substrats) et la topographie (sommet et pentes), facteurs clés avec le temps qui influencent la pédogénèse. Nous avons étudié sept placettes permanentes de forêt naturelle du réseau Guyafor. Nous avons observé des sols homogènes et présentant de meilleures propriétés physiques (sols à drainage vertical libre) au nord-est de la Guyane, région avec les plus fortes pluviosités. Par contre, les sols observés au nord-ouest, région avec de plus faibles pluviosités, ont des propriétés physiques variables selon la topographie et la géologie. L'effet direct de la pluviosité reste cependant incertain compte-tenu d'un dispositif expérimental incomplet. Nous avons aussi observé que la géologie et la topographie exerçaient une influence sur les propriétés chimiques des sols au travers de la texture. Nous avons observé des corrélations positives entre argile, carbone et capacité d'échange cationique et des corrélations négatives entre argile et phosphore assimilable. D'après ces résultats, on s'attend à ce que la productivité et la biomasse de la forêt soient les plus importantes dans les régions avec les pluviosités les plus élevées et avec soient variables en lien avec la topographie et la géologie dans les régions de pluviosités plus faibles
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