Some Thoughts on the Reporting of Adverse Events in Phase II Cancer Clinical Trials
Author:
Affiliation:
1. National Surgical Adjuvant Breast and Bowel Project Biostatistical Center, University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA
Publisher
American Society of Clinical Oncology (ASCO)
Subject
Cancer Research,Oncology
Link
http://ascopubs.org/doi/pdfdirect/10.1200/JCO.2006.06.9856
Reference5 articles.
1. Adverse Event Reporting in Publications Compared With Sponsor Database for Cancer Clinical Trials
2. Dealing With a Deluge of Data: An Assessment of Adverse Event Data on North Central Cancer Treatment Group Trials
3. Early Detection of Toxicity and Adjustment of Ongoing Clinical Trials: The History and Performance of the North Central Cancer Treatment Group’s Real-Time Toxicity Monitoring Program
4. The Reliability of Medical Record Review for Estimating Adverse Event Rates
5. Mortality Associated With Irinotecan Plus Bolus Fluorouracil/Leucovorin: Summary Findings of an Independent Panel
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