Exploring differences in adverse symptom event grading thresholds between clinicians and patients in the clinical trial setting

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Symptom Monitoring in Pediatric Oncology Using Patient-Reported Outcomes: Why, How, and Where Next.Treatment of anemia in patients with solid tumors receiving chemotherapy in palliative setting: usual practice versus guidelines.

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Exploring differences in adverse symptom event grading thresholds between clinicians and patients in the clinical trial setting

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 16 January 2017

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Exploring differences in adver ...... in the clinical trial setting

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Exploring differences in adver ...... in the clinical trial setting.

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Exploring differences in adver ...... in the clinical trial setting

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Exploring differences in adver ...... in the clinical trial setting.

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Exploring differences in adver ...... in the clinical trial setting

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Exploring differences in adver ...... in the clinical trial setting.

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P1476

Exploring differences in adver ...... in the clinical trial setting

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Antonia V Bennett

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Lauren J Rogak

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Liora P Stark

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Mary Shaw

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Narre Heon

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Sean J Ryan

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Thomas M Atkinson

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Yuelin Li

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Intraclass correlations: uses in assessing rater reliability

Cognitive interviewing of the US National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Development of the National Cancer Institute's patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE).

The missing voice of patients in drug-safety reporting.

Evaluation of an online platform for cancer patient self-reporting of chemotherapy toxicities.

Reliability of adverse symptom event reporting by clinicians.

Validity and Reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Symptom Monitoring With Patient-Reported Outcomes During Routine Cancer Treatment: A Randomized Controlled Trial.

Patient-reported outcomes and the evolution of adverse event reporting in oncology.

Adverse symptom event reporting by patients vs clinicians: relationships with clinical outcomes

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s00432-016-2335-9

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735-743

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scholarly article

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10.1007/S00432-016-2335-9

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143

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Ethan Basch

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2017-01-16T00:00:00Z

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28093637

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Exploring differences in adverse symptom event grading thresholds between clinicians and patients in the clinical trial setting

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P2860

P2860

Exploring differences in adverse symptom event grading thresholds between clinicians and patients in the clinical trial setting

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932