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    Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has…

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    • Happy to share the publication of updated 12-year results of SOFT (TEXT/SOFT coming soon!) @etop_ibcsg @BIGagainstBC @BCTrialsANZ Adjuvant Endocrine Therapy in Premenopausal Breast Cancer: 12-Year Results From SOFT https://t.co/h7HQfxF8vN

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    This paper provides guidance for researchers with some mathematical background on the conduct of time-to-event analysis in observational studies based on intensity (hazard) models. Discussions of basic concepts like time axis, event definition and censoring are given. Hazard models are introduced, w …

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    • 2 must read papers highlighted in this talk: STRATOS initiative, principles of survival endpoints. Read or skip the theory, accessible for all. https://t.co/cZ619r0ykP Selection bias. Analysis with biospecimen assmt after survival endpt time origin. https://t.co/banj0Ad32O https://t.co/M1vOeq7TrQ

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    During recent years, the burden of bureaucracy in clinical research has increased dramatically, adversely impacting the activity of investigators and clinical research teams. Although compliance with the Declaration of Helsinki, the guidelines for Good Clinical Practice (GCP), and other applicable regulations remains unquestionable, their overinterpretation and substitution by the internal…

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    • GCP refresher today. It starts: ICH mission to achieve grtr harmonization to ensure safe, effective, high quality medicines r developed & registered ➡️ in the most resource-efficient manner ⬅️ Oh how we’ve strayed. I support @myESMO efforts https://t.co/j7Prv5jb1v

  • Mashup Score: 5

    During recent years, the burden of bureaucracy in clinical research has increased dramatically, adversely impacting the activity of investigators and clinical research teams. While compliance with the Declaration of Helsinki, the Guidelines for Good Clinical Practice (GCP) and other applicable regulations remains unquestionable, their overinterpretation and substitution by the internal operating…

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    • Thank you @myESMO Streamlining clinical research: An ESMO awareness call to improve Sponsoring and Monitoring of Clinical Trials. - Ann Oncol. “…a platform for discussion…promoting sustainability of clinical research and the care of cancer patients” https://t.co/j7Prv51zCV

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    An intensive workshop in the essentials of effective clinical trial designs of therapeutic interventions in the treatment of cancer for clinical fellow and junior faculty clinical researchers in all oncology subspecialties, including radiation and surgical oncology and radiology. AACR/ASCO Methods in Clinical Cancer Research WorkshopJuly 24-30, 2022The Hythe Vail, Vail,…

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    • @Eddie_Cliff @RahulBanerjeeMD @tmprowell Sponsored by @AACR and @ASCO , week long workshop training for fellows and early career docs interested in cancer clinical trials. Incredible experience for all involved. #VailWorkshop https://t.co/xl97yO29LG