Skip to main content

Table 1 Demographic Information (N = 1859)

From: Establishing a common metric for patient-reported outcomes in cancer patients: linking patient reported outcomes measurement information system (PROMIS), numerical rating scale, and patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE)

Assessment Condition

 IVRS

602 (32.4%)

 Paper

654 (35.2%)

 Web

603 (32.4%)

Treatment Site

 MD Anderson

354 (19.0%)

 Mayo Clinic

858 (46.2%)

 Memorial-Sloan Kettering

149 (8.0%)

 Northwestern University

434 (23.3%)

 University of North Carolina

64 (3.4%)

Age

 Mean (SD)

56.4 (12.5)

 Q1, Median, Q3

49.0, 58.0, 65.0

 Range

(18.0–89.0)

Gender

 F

1131 (61.0%)

 M

722 (39.0%)

 Missing

6

Race: On Study Form

 White

1367 (73.8%)

 Black or African American

407 (22.0%)

 Asian

54 (2.9%)

 American Indian or Alaska Native

5 (0.3%)

 Not reported: patient refused or not available

10 (0.5%)

 Unknown: Patient unsure

10 (0.5%)

 Missing

6

Ethnicity: On Study Form

 Hispanic or Latino

106 (5.7%)

 Not Hispanic or Latino

1729 (93.3%)

 Not reported: Patient refused or data not available

12 (0.6%)

 Unknown: Patient is unsure of their ethnicity

6 (0.3%)

 Missing

6

Disease

 Breast

462 (25.9%)

 Lymphoma/myeloma

370 (20.8%)

 Prostate/bladder

21 (1.2%)

 Lung

136 (7.6%)

 Colorectal

177 (9.9%)

 Head/neck/gastroesophageal

158 (8.9%)

 Other

457 (25.7%)

 Missing

78

PS on Checklist

 

 0

853 (46.0%)

 1

838 (45.2%)

 2

139 (7.5%)

 3

22 (1.2%)

 4

1 (0.1%)

 Missing

6

Disease Stage

 I

207 (11.8%)

 II

375 (21.4%)

 III

518 (29.5%)

 IV

654 (37.3%)

 Missing

105

Education Level: On Study Form

 Less Than High School

104 (5.9%)

 High School or GED

413 (23.3%)

 Some College

524 (29.5%)

 College Graduate or More

735 (41.4%)

 Missing

83