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Adverse Event Burden Score-A Versatile Summary Measure for Cancer Clinical Trials.
Le-Rademacher, Jennifer G; Hillman, Shauna; Storrick, Elizabeth; Mahoney, Michelle R; Thall, Peter F; Jatoi, Aminah; Mandrekar, Sumithra J.
Afiliação
  • Le-Rademacher JG; Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
  • Hillman S; Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
  • Storrick E; Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
  • Mahoney MR; IQVIA, Raleigh-Durham, NC 27703, USA.
  • Thall PF; Department of Biostatistics, M.D. Anderson Cancer Center, Houston, TX 77230, USA.
  • Jatoi A; Department of Oncology, Mayo Clinic, Rochester, MN 55905, USA.
  • Mandrekar SJ; Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
Cancers (Basel) ; 12(11)2020 Nov 04.
Article em En | MEDLINE | ID: mdl-33158080
ABSTRACT
This article introduces the adverse event (AE) burden score. The AE burden by treatment cycle is a weighted sum of all grades and AEs that the patient experienced in a cycle. The overall AE burden score is the total AE burden the patient experienced across all treatment cycles. AE data from two completed Alliance multi-center randomized double-blind placebo-controlled trials, with different AE profiles (NCCTG 97-24-51 176 patients, and A091105 83 patients), were utilized for illustration. Results of the AE burden score analyses corroborated the trials' primary results. In 97-24-51, the overall AE burden for patients on the treatment arm was 2.2 points higher than those on the placebo arm, with a higher AE burden for patients who went off treatment early due to AE. Similarly, in A091105, the overall AE burden was 1.6 points higher on the treatment arm. On the placebo arms, the AE burden in 97-24-51 remained constant over time; and increased in later cycles in A091105, likely attributable to the increase in disease morbidity. The AE burden score enables statistical comparisons analogous to other quantitative endpoints in clinical trials, and can readily accommodate different trial settings, diseases, and treatments, with diverse AE profiles.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2020 Tipo de documento: Article