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. 2023 Dec 13;6(12):e2347449. doi: 10.1001/jamanetworkopen.2023.47449

Table 1. Demographic and Clinical Characteristics of CHIIP Study Participants Compared With the Overall CCSS Cohort.

Characteristics Participants, No. (%)
CHIIP (n = 293) CCSS (n = 11 337)a
Age, median (range) at assessment, y 39.9 (21.5-65.0) 36.8 (16.0-65.9)
Sex
Male 149 (50.9) 5419 (47.8)
Female 144 (49.2) 5918 (52.2)
Race
American Indian or Alaska Native 0 55 (0.5)
Asian 5 (1.7) 160 (1.6)
Black 7 (2.4) 498 (4.6)
Pacific Islander 2 (0.7) 10 (0.1)
White 267 (91.1) 10195 (89.3)
>1 Race or otherb 12 (4.1) 318 (3.1)
Unknown 0 101 (0.9)
Ethnicity
Hispanic or Latino 23 (7.8) 710 (6.5)
Not Hispanic or Latino 270 (92.2) 10537 (92.7)
Unknown 0 90 (0.9)
Age at diagnosis, median (range), y 9.3 (0.0-20.9) 7.3 (0.0-21.0)
Cancer diagnosis
Bone cancer 36 (12.3) 951 (7.4)
Central nervous system tumor 23 (7.9) 2000 (15.5)
Hodgkin lymphoma 60 (20.5) 1380 (10.7)
Kidney tumor 32 (10.9) 1070 (8.3)
Leukemia 94 (32.1) 3384 (38.4)
Non-Hodgkin lymphoma 23 (7.9) 936 (7.2)
Neuroblastoma 14 (4.8) 843 (6.5)
Soft tissue sarcoma 11 (3.8) 773 (6.0)
Cancer treatment exposuresc
Anthracycline chemotherapy 222 (75.8) 8689 (83.0)
Any radiation 203 (69.3) 5906 (50.8)
Self-reported health care insurance 273 (93.2) 10 477 (92.6)
Self-reported routine care visit within past 2 y 262 (89.4) 10 324 (91.3)
Self-reported history of diagnosed cardiovascular conditions
Hypertension 94 (32.1) 2019 (16.3)
Dyslipidemia 109 (37.2) 2395 (19.9)
Diabetes 34 (11.6) 659 (5.6)
Prediabetes 22 (7.5) 498 (4.1)

Abbreviations: CCSS, Childhood Cancer Survivor Study; CHIIP, Communicating Health Information and Improving Coordination With Primary Care.

a

Members of the cohort who responded to the follow-up 5 survey, conducted between 2014 and 2016.

b

Includes those who self-reported as other or nonspecified.

c

Per CCSS records.