Composite grading algorithm for National Cancer Institute’s PRO-CTCAE.

Author:

Dueck Amylou C.1,Becker Claus C.2,Rogak Lauren J.3,Schrag Deborah4,Reeve Bryce5,Spears Patricia6,Smith Mary Lou7,Gounder Mrinal M.8,Mahoney Michelle R.9,Schwartz Gary K.10,Bennett Antonia Vickery11,Mendoza Tito R.12,Cleeland Charles S.12,Sloan Jeff A.9,Bruner Deborah13,Schwab Gisela14,Atkinson Thomas Michael8,Thanarajasingam Gita15,Bertagnolli Monica M.16,Basch Ethan M.17

Affiliation:

1. Mayo Clinic, Scottsdale, AZ;

2. Deciphera Pharmaceuticals, LLC, Waltham, MA;

3. Memorial Sloan-Kettering Cancer Center, New York, NY;

4. Dana-Farber Cancer Institute, Boston, MA;

5. Duke University School of Medicine, Durham, NC;

6. Cancer Information and Support Network, Raleigh, NC;

7. Research Advocacy Network, Naperville, IL;

8. Memorial Sloan Kettering Cancer Center, New York, NY;

9. Mayo Clinic, Rochester, MN;

10. Columbia University Irving Medical Center, New York, NY;

11. University of North Carolina, Chapel Hill, Lineberger Comprehensive Cancer Center, Chapel Hill, NC;

12. Department of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, TX;

13. Winship Cancer Institute at Emory University, Atlanta, GA;

14. Exelixis, Inc., South San Francisco, CA;

15. Division of Hematology, Mayo Clinic, Rochester, MN;

16. Dana-Farber/ Partners CancerCare, Harvard Medical School, Boston, MA;

17. UNC Lineberger Comprehensive Cancer Center, Chapel Hill, NC;

Abstract

7018 Background: Standard reporting of symptomatic adverse events (AEs) in oncology relies on clinicians to rate patient (pt) experience using CTCAE; each symptom is represented by a single graded item. To capture direct pt experience, NCI developed PRO-CTCAE to supplement CTCAE. In PRO-CTCAE, the pt answers up to 3 questions per AE about a symptom’s frequency, severity and interference with daily activities. To align PRO-CTCAE with CTCAE, we developed an algorithm for mapping sets of questions for an AE to a single composite numerical grade. Methods: We used a 5-step process. (1) All 187 possible PRO-CTCAE score permutations were presented to clinical investigators to subjectively map permutations to single numerical grades (range 0-3). (2) Permutations with < 75% agreement were presented to investigator committees at a National Clinical Trials Network 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 AEs between study arms was measured in 2 phase III clinical trials (Alliance for Clinical Trials in Oncology A091105 and Exelixis COMET-2). Results: (1) 12/187 score permutations had < 75% initial agreement. (2) Majority consensus was reached for all permutations. (3) 5 mappings were adjusted to assure directional consistency. (4) Composite grades for 46/59 (78%) AEs were higher in pts with ECOG performance status 2-4 vs 0-1 (median effect size 0.23 [range -0.49-0.73]; 32/59 effect size ≥0.2; 25/59 p< 0.05), similar to when conducting analysis on individual unmapped items. The test-retest reliability for 24 selected composite grades ranged from 0.57-0.96 (median intraclass correlation coefficient [ICC] 0.77) with 18/24 (75%) grades having ICC ≥0.7. Median (range) standardized response means in pts reporting worsening, no change, and improvement were 0.20 (0.03-0.34), -0.06 (-0.20-0.03) and -0.12 (-0.32-0.06). (5) Pattern, directionality and statistical significance of between-arm differences in both trials were preserved with composite grades as compared to individual unmapped items. Conclusions: A composite grading algorithm for PRO-CTCAE was rigorously developed and validated. PRO-CTCAE composite grades may be useful in analyses to provide a single metric for each pt-reported AE for trial and real-world reporting. Support: UG1CA189823; U01CA233046; HHSN261200800043C; Bayer (A091105); https://acknowledgments.alliancefound.org .

Funder

U.S. National Institutes of Health

Pharmaceutical/Biotech Company

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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