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Standardizing patient-reported outcomes assessment in cancer clinical trials: a patient-reported outcomes measurement information system initiative.

Publication ,  Journal Article
Garcia, SF; Cella, D; Clauser, SB; Flynn, KE; Lad, T; Lai, J-S; Reeve, BB; Smith, AW; Stone, AA; Weinfurt, K
Published in: J Clin Oncol
November 10, 2007

Patient-reported outcomes (PROs), such as symptom scales or more broad-based health-related quality-of-life measures, play an important role in oncology clinical trials. They frequently are used to help evaluate cancer treatments, as well as for supportive and palliative oncology care. To be most beneficial, these PROs must be relevant to patients and clinicians, valid, and easily understood and interpreted. The Patient-Reported Outcomes Measurement Information System (PROMIS) Network, part of the National Institutes of Health Roadmap Initiative, aims to improve appreciably how PROs are selected and assessed in clinical research, including clinical trials. PROMIS is establishing a publicly available resource of standardized, accurate, and efficient PRO measures of major self-reported health domains (eg, pain, fatigue, emotional distress, physical function, social function) that are relevant across chronic illnesses including cancer. PROMIS is also developing measures of self-reported health domains specifically targeted to cancer, such as sleep/wake function, sexual function, cognitive function, and the psychosocial impacts of the illness experience (ie, stress response and coping; shifts in self-concept, social interactions, and spirituality). We outline the qualitative and quantitative methods by which PROMIS measures are being developed and adapted for use in clinical oncology research. At the core of this activity is the formation and application of item banks using item response theory modeling. We also present our work in the fatigue domain, including a short-form measure, as a sample of PROMIS methodology and work to date. Plans for future validation and application of PROMIS measures are discussed.

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Published In

J Clin Oncol

DOI

EISSN

1527-7755

Publication Date

November 10, 2007

Volume

25

Issue

32

Start / End Page

5106 / 5112

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Sickness Impact Profile
  • Reproducibility of Results
  • Quality of Life
  • Quality Indicators, Health Care
  • Psychometrics
  • Patient Satisfaction
  • Oncology & Carcinogenesis
  • Neoplasms
  • Humans
 

Citation

APA
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Garcia, S. F., Cella, D., Clauser, S. B., Flynn, K. E., Lad, T., Lai, J.-S., … Weinfurt, K. (2007). Standardizing patient-reported outcomes assessment in cancer clinical trials: a patient-reported outcomes measurement information system initiative. J Clin Oncol, 25(32), 5106–5112. https://doi.org/10.1200/JCO.2007.12.2341
Garcia, Sofia F., David Cella, Steven B. Clauser, Kathryn E. Flynn, Thomas Lad, Jin-Shei Lai, Bryce B. Reeve, Ashley Wilder Smith, Arthur A. Stone, and Kevin Weinfurt. “Standardizing patient-reported outcomes assessment in cancer clinical trials: a patient-reported outcomes measurement information system initiative.J Clin Oncol 25, no. 32 (November 10, 2007): 5106–12. https://doi.org/10.1200/JCO.2007.12.2341.
Garcia SF, Cella D, Clauser SB, Flynn KE, Lad T, Lai J-S, et al. Standardizing patient-reported outcomes assessment in cancer clinical trials: a patient-reported outcomes measurement information system initiative. J Clin Oncol. 2007 Nov 10;25(32):5106–12.
Garcia, Sofia F., et al. “Standardizing patient-reported outcomes assessment in cancer clinical trials: a patient-reported outcomes measurement information system initiative.J Clin Oncol, vol. 25, no. 32, Nov. 2007, pp. 5106–12. Pubmed, doi:10.1200/JCO.2007.12.2341.
Garcia SF, Cella D, Clauser SB, Flynn KE, Lad T, Lai J-S, Reeve BB, Smith AW, Stone AA, Weinfurt K. Standardizing patient-reported outcomes assessment in cancer clinical trials: a patient-reported outcomes measurement information system initiative. J Clin Oncol. 2007 Nov 10;25(32):5106–5112.

Published In

J Clin Oncol

DOI

EISSN

1527-7755

Publication Date

November 10, 2007

Volume

25

Issue

32

Start / End Page

5106 / 5112

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Sickness Impact Profile
  • Reproducibility of Results
  • Quality of Life
  • Quality Indicators, Health Care
  • Psychometrics
  • Patient Satisfaction
  • Oncology & Carcinogenesis
  • Neoplasms
  • Humans