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Table 1 QLQ-CIPN20, PRO-CTCAE™, and TNSc© Sample statistics at each study visit

From: Measurement properties of brief neuropathy screening items in cancer patients receiving taxanes, platinums, or proteasome inhibitors

Measure

Mean (SD)

Median (range)

Proportion at floor (%)

Proportion at ceiling (%)

PRO-CTCAE numbness and tingling severity

    

T1 (n = 140)

0.79 (0.78)

1 (0–3)

57 (40.7%)

0

T2 (n = 137)

0.91 (0.84)

1 (0–3)

50 (36.5%)

0

T3 (n = 138)

1.08 (0.88)

1 (0–4)

40 (29%)

1 (0.07%)

T4 (n = 123)

1.03 (0.83)

1 (0–3)

35 (28.5%)

0

PRO-CTCAE numbness and tingling interference

    

T1 (n = 139)

0.25 (0.54)

0 (0–2)

111 (79.9%)

0

T2 (n = 140)

0.49 (0.79)

0 (0–3)

93 (66.4%)

0

T3 (n = 138)

0.55 (0.76)

0 (0–3)

83 (60.1%)

0

T4 (n = 126)

0.52 (0.72)

0 (0–3)

76 (60.3%)

0

QLQ-CIPN20 sensory

    

T1 (n = 140)

7.84 (10.51)

3.70 (0–55.56

56 (40%)

0

T2 (n = 140)

11.02 (11.02)

7.41 (0–55.56)

33 (23.6%)

0

T3 (n = 138)

11.92 (11.88)

7.41 (0–55.56)

33 (23.9%)

0

QLQ-CIPN20 motor

    

T1 (n = 140)

5.15 (7.60)

0 (0–37.5)

75 (53.6%)

0

T2 (n = 139)

7.61 (9.74)

4.17 (0–50)

58 (41.7%)

0

T3 (n = 138)

8.49 (10.57)

4.17 (0–54.17)

54 (39.1%)

0

010 NRS of worst CIPN pain Intensity

    

T1 (n = 138)

1.41 (1.98)

0 (0–9)

71 (51.4%)

0

T2 (n = 139)

1.99 (2.41)

1 (0–10)

61 (43.9%)

0

T3 (n = 138)

1.97 (2.16)

1 (0–9)

58 (42%)

0

TNSc©

    

T3 (n = 118)

6.75 (2.9)

7 (1–13)

0

0

  1. Table describes sample statistics for PRO-CTCAE item (Range = 0–4) QLQ-CIPN20 sensory and motor subscale (Range = 0–100), 0–10 NRS of worst CIPN pain intensity (Range = 0–10) and TNSc© (Range = 0–20) scores at each study time point (T1–T4). Higher scores on all measures represent worse CIPN severity
  2. CIPN-Chemotherapy-Induced Peripheral Neuropathy, PRO-CTCAE™—Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events, QLQ-CIPN20-Quality of Life Questionnaire-Chemotherapy-Induced Peripheral Neuropathy Scale, TNSc©—Total Neuropathy Score-Clinical Version