Composite grading algorithm for the National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

被引:121
作者
Basch, Ethan [1 ,2 ]
Becker, Claus [3 ]
Rogak, Lauren J. [2 ]
Schrag, Deborah [4 ]
Reeve, Bryce B. [5 ]
Spears, Patricia [1 ]
Smith, Mary Lou [6 ]
Gounder, Mrinal M. [2 ]
Mahoney, Michelle R. [7 ]
Schwartz, Gary K. [8 ]
Bennett, Antonia, V [1 ]
Mendoza, Tito R. [9 ]
Cleeland, Charles S. [9 ]
Sloan, Jeff A. [7 ]
Bruner, Deborah Watkins [10 ]
Schwab, Gisela [11 ]
Atkinson, Thomas M. [2 ]
Thanarajasingam, Gita [12 ]
Bertagnolli, Monica M. [13 ]
Dueck, Amylou C. [14 ]
机构
[1] Univ N Carolina, UNC Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA
[2] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[3] Deciphera Pharmaceut, Waltham, MA USA
[4] Harvard Canc Ctr, Dana Farber Partners Canc Care, Boston, MA USA
[5] Duke Univ, Med Ctr, Duke Canc Inst, Durham, NC USA
[6] Res Advocacy Network, Plano, TX USA
[7] Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA
[8] Columbia Univ, New York, NY USA
[9] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[10] Emory Univ Hosp, Winship Canc Inst, 1364 Clifton Rd NE, Atlanta, GA 30322 USA
[11] Exelixis Inc, San Francisco, CA USA
[12] Mayo Clin, Div Hematol, Rochester, MN USA
[13] Brigham & Womens Hosp, Alliance Off Grp Chair, 75 Francis St, Boston, MA 02115 USA
[14] Mayo Clin, Alliance Stat & Data Ctr, 13400 E Shea Blvd, Scottsdale, AZ 85259 USA
关键词
Adverse event; patient-reported outcome; toxicity; health-related quality of life; oncology; symptom; Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events; Common Terminology Criteria for Adverse Events;
D O I
10.1177/1740774520975120
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events is an item library designed for eliciting patient-reported adverse events in oncology. For each adverse event, up to three individual items are scored for frequency, severity, and interference with daily activities. To align the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events with other standardized tools for adverse event assessment including the Common Terminology Criteria for Adverse Events, an algorithm for mapping individual items for any given adverse event to a single composite numerical grade was developed and tested. Methods: A five-step process was used: (1) All 179 possible Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events score combinations were presented to 20 clinical investigators to subjectively map combinations to single numerical grades ranging from 0 to 3. (2) Combinations with <75% agreement were presented to investigator committees at a National Clinical Trials Network cooperative group meeting to gain majority consensus via anonymous voting. (3) The resulting algorithm was refined via graphical and tabular approaches to assure directional consistency. (4) Validity, reliability, and sensitivity were assessed in a national study dataset. (5) Accuracy for delineating adverse events between study arms was measured in two Phase III clinical trials (NCT02066181 and NCT01522443). Results: In Step 1, 12/179 score combinations had <75% initial agreement. In Step 2, majority consensus was reached for all combinations. In Step 3, five grades were adjusted to assure directional consistency. In Steps 4 and 5, composite grades performed well and comparably to individual item scores on validity, reliability, sensitivity, and between-arm delineation. Conclusion: A composite grading algorithm has been developed and yields single numerical grades for adverse events assessed via the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events, and can be useful in analyses and reporting.
引用
收藏
页码:104 / 114
页数:11
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