Feasibility of Implementing the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events in a Multicenter Trial: NCCTG N1048

被引:52
|
作者
Basch, Ethan [1 ,3 ]
Dueck, Amylou C. [4 ]
Rogak, Lauren J. [3 ]
Mitchell, Sandra A. [5 ]
Minasian, Lori M. [5 ]
Denicoff, Andrea M. [5 ]
Wind, Jennifer K. [6 ]
Shaw, Mary C. [3 ]
Heon, Narre [3 ]
Shi, Qian [7 ]
Ginos, Brenda [4 ]
Nelson, Garth D. [7 ]
Meyers, Jeffrey P. [7 ]
Chang, George J. [8 ]
Mamon, Harvey J. [6 ]
Weiser, Martin R. [3 ]
Kolevska, Tatjana [9 ]
Reeve, Bryce B. [2 ]
Bruner, Deborah Watkins [10 ]
Schrag, Deborah [6 ]
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, 170 Manning Dr, Chapel Hill, NC 27516 USA
[2] Duke Univ, Med Ctr, Duke Canc Inst, Durham, NC USA
[3] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[4] Mayo Clin, Alliance Stat & Data Ctr, Scottsdale, AZ USA
[5] NCI, Rockville, MD USA
[6] Dana Farber Partners CancerCare, Boston, MA USA
[7] Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA
[8] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[9] Kaiser Permanente Vallejo Med Ctr, Vallejo, CA USA
[10] Emory Univ, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1200/JCO.2018.78.8620
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeThe US National Cancer Institute (NCI) Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) was developed to enable patient reporting of symptomatic adverse events in oncology clinical research. This study was designed to assess the feasibility and resource requirements associated with implementing PRO-CTCAE in a multicenter trial.MethodsPatients with locally advanced rectal cancer enrolled in the National Cancer Institute-sponsored North Central Cancer Treatment Group (Alliance) Preoperative Radiation or Selective Preoperative Radiation and Evaluation before Chemotherapy and Total Mesorectal Excision trial were asked to self-report 30 PRO-CTCAE items weekly from home during preoperative therapy, and every 6 months after surgery, via either the Web or an automated telephone system. If participants did not self-report within 3 days, a central coordinator called them to complete the items. Compliance was defined as the proportion of participants who completed PRO-CTCAE assessments at expected time points.ResultsThe prespecified PRO-CTCAE analysis was conducted after the 500th patient completed the 6-month follow-up (median age, 56 years; 33% female; 12% nonwhite; 43% high school education or less; 5% Spanish speaking), across 165 sites. PRO-CTCAE was reported by participants at 4,491 of 4,882 expected preoperative time points (92.0% compliance), of which 3,771 (77.2%) were self-reported by participants and 720 (14.7%) were collected via central coordinator backup. Compliance at 6-month post-treatment follow-up was 333 of 468 (71.2%), with 122 (26.1%) via backup. Site research associates spent a median of 15 minutes on PRO-CTCAE work for each patient visit. Work by a central coordinator required a 50% time commitment.ConclusionHome-based reporting of PRO-CTCAE in a multicenter trial is feasible, with high patient compliance and low site administrative requirements. PRO-CTCAE data capture is improved through centralized backup calls.
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收藏
页码:3120 / +
页数:10
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