Jose Escarce
National Institutes of Health
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Featured researches published by Jose Escarce.
Journal of Clinical Oncology | 2003
Joy H. Lewis; Meredith L. Kilgore; Dana P. Goldman; Edward L. Trimble; Richard S. Kaplan; Michael Montello; Michael G. Housman; Jose Escarce
PURPOSE Although 61% of new cases of cancer occur among the elderly, recent studies indicate that the elderly comprise only 25% of participants in cancer clinical trials. Further investigation into the reasons for low elderly participation is warranted. Our objective was to evaluate the participation of the elderly in clinical trials sponsored by the National Cancer Institute (NCI) and assess the impact of protocol exclusion criteria on elderly participation. PATIENTS AND METHODS We conducted a retrospective analysis using NCI data, analyzing patient and trial characteristics for 59,300 patients enrolled onto 495 NCI-sponsored, cooperative group trials, active from 1997 through 2000. Our main outcome measure was the proportion of elderly patients enrolled onto cancer clinical trials compared with the proportion of incident cancer patients who are elderly. RESULTS Overall, 32% of participants in phase II and III clinical trials were elderly, compared with 61% of patients with incident cancers in the United States who are elderly. The degree of underrepresentation was more pronounced in trials for early-stage cancers than in trials for late-stage cancers (P <.001). Furthermore, protocol exclusion criteria on the basis of organ-system abnormalities and functional status limitations were associated with lower elderly participation. We estimate that if protocol exclusions were relaxed, elderly participation in cancer trials would be 60%. CONCLUSION The elderly are underrepresented in cancer clinical trials relative to their disease burden. Older patients are more likely to have medical histories that make them ineligible for clinical trials because of protocol exclusions. Insurance coverage for clinical trials is one step toward improvement of elderly access to clinical trials. Without a change in study design or requirements, this step may not be sufficient.
Archive | 2005
Melinda Beeuwkes Buntin; Partha Deb; Jose Escarce; Carrie Hoverman; Susan M. Paddock; Neeraj Sood
RAND Technical Report | 2005
Melinda Beeuwkes Buntin; Jose Escarce; Carrie Hoverman; Susan M. Paddock; Mark E. Totten; Barbara O. Wynn
Archive | 2002
Geoffrey F. Joyce; Jose Escarce; David Solomon; Dana P. Goldman
Archive | 2003
Melinda Beeuwkes Buntin; Jose Escarce; Dana P. Goldman; Paul G Shekelle; Miriam Laugesen; Hongjan Kan; Eileen McKinnon; Shannon Rhodes
Archive | 2000
Dana P. Goldman; John L. Adams; Sandra H. Berry; Jose Escarce; Meredith L. Kilgore
RAND Technical Report | 2006
Melinda Beeuwkes Buntin; Susan M. Paddock; Jose Escarce; Orla Hayden
Archive | 2003
Melinda Beeuwkes Buntin; Jose Escarce; Dana P. Goldman; Paul G Shekelle; Miriam Laugesen; Hongjan Kan; Eileen McKinnon; Shannon Rhodes
Archive | 2013
Teryl K. Nuckols; Jose Escarce; Steven M. Asch
Archive | 2010
Peter J. Huckfeldt; Jose Escarce; David C. Grabowski; Joseph P. Newhouse; Neeraj Sood