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. 2022 Oct 28;14(21):5310. doi: 10.3390/cancers14215310

Table 2.

Demographics of patients for whom we have data on QoL at T0.

Patients Aged 4–17 Years Whose Parents Reported on QoL at T0 (n = 109) Patients Aged 12–17 Years Who Self-Reported on QoL at T0 (n = 23)
Age, years
Mean (SD) 11.3 (4.2) 14.8 (1.9)
Median (IQR) 12 (8, 15) 15 (13, 17)
Range 4–17 12–17
Gender, n (%)
Female 49 (45%) 14 (61%)
Male 60 (55%) 9 (39%)
Age of patient at time of diagnosis, years
Mean (SD) 10.0 (4.5) 13.0 (2.8)
Median (IQR) 10 (6, 14) 13.5 (11, 15.25)
Range 0–17 7–17
Diagnosis, n (%)
Central Nervous System 42 (39%) 5 (22%)
Sarcoma 34 (31%) 12 (52%)
Leukemia/Lymphoma 14 (13%) 4 (17%)
Neuroblastoma 9 (8%) 0 (0%)
Other 10 (9%) 2 (9%)
Number of relapses for patient prior to PRISM consent, n (%)
0 46 (42%) 11 (48%)
1 47 (43%) 10 (44%)
≥2 16 (15%) 2 (9%)
Received cancer treatment while awaiting testing results
Yes 87 (79.8%) 20 (87%)
No 22 (20.2%) 3 (13%)
Time (days) from initial cancer diagnosis * to PRISM enrolment
Median (IQR) 418.5 (11.5, 818) 359 (83, 699)
Range 0–5586 1–4023
Time (days) from cancer event ** resulting in patient being eligible for PRISM and enrolment
Median (IQR) 6 (1, 16.5) 7 (1, 49)
Range 0–834 0–155

* Some participants have been diagnosed with more than one type of cancer in their lifetime; ** Initial diagnosis, relapse or disease progression; SD = standard deviation; n = number; QoL = Quality of Life.