Articles with "symptomatic adverse" as a keyword



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Identifying symptomatic adverse events using the patient‐reported outcomes version of the common terminology criteria for adverse events in patients with non‐small cell lung cancer with epidermal growth factor receptor exon 20 insertion mutations

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Published in 2022 at "Cancer Medicine"

DOI: 10.1002/cam4.5376

Abstract: Tolerability and safety of treatments are important in oncology trials and should be informed by patient assessments. We identified the most relevant patient‐reported symptomatic adverse events (AEs) to measure in patients with non‐small cell lung… read more here.

Keywords: non small; patient reported; patients non; symptomatic adverse ... See more keywords

Commentary on King-Kallimanis et al.: Inadequate measurement of symptomatic adverse events in immunotherapy registration trials

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Published in 2019 at "Clinical Trials"

DOI: 10.1177/1740774519836989

Abstract: Symptomatic adverse events are common with cancer therapies, and provide key information about tolerability during development and regulatory review. After a therapy becomes available on the market, information about these adverse events is essential for… read more here.

Keywords: information; symptomatic adverse; adverse events; oncology ... See more keywords

Timing is everything: The importance of patient-reported outcome assessment frequency when characterizing symptomatic adverse events

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Published in 2022 at "Clinical Trials"

DOI: 10.1177/17407745221093935

Abstract: Objective Although patient-reported symptoms and side effects are increasingly measured in cancer clinical trials, an appropriate assessment frequency has not yet been established. To determine whether differences in assessment frequency affect the apparent incidence and… read more here.

Keywords: patient reported; reported outcome; patient; symptomatic adverse ... See more keywords

Lack of Concordance in Symptomatic Adverse Event Reporting by Children, Clinicians, and Caregivers: Implications for Cancer Clinical Trials

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Published in 2022 at "Journal of Clinical Oncology"

DOI: 10.1200/jco.21.02669

Abstract: PURPOSE To examine concordance in symptomatic adverse event (AE) grading using the Common Terminology Criteria for Adverse Events (CTCAE 4.0) for clinicians and its patient-reported outcome (PRO) versions for children (Ped-PRO-CTCAE) and caregivers (Ped-PRO-CTCAE [Caregiver]).… read more here.

Keywords: clinicians caregivers; concordance; symptomatic adverse; adverse event ... See more keywords