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Table 1 Demographic and clinical characteristics Round 1(n = 100) and Round 2 (n = 10)

From: Dutch translation and linguistic validation of the U.S. National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE™)

Participant characteristics

Round 1

n = 100

Round 2

n = 10a

Age

 Mean (SD)

59.3 years (±12.1)

63,4 (±8.5)

 Range in years

28–85

51–80

 % > 65 years of age

34%

30%

Sex n (%)

 Female

51 (51)

4 (40)

 Male

57 (57)

6 (60)

Education

 Mean years (SD)

14.4 (2.3)

12.0 (1,6)

 % lower than high school: (or nearest equivalent)

7

20

 % high school or higher: (or nearest equivalent)

93

50

 Missing (%)

0

30

Type of treatment n (%)b

 Combined Chemo-radiotherapy

36 (36)

5 (50)

 Chemotherapy

26 (26)

5 (50)

 Radiotherapy

39 (39)

2 (20)

 Hormonal therapy

13 (13)

1 (10)

 Part of clinical trial

5 (5)

0 (0)

 Immune therapy

10 (10)

0 (0)

 Molecularly targeted therapy

8 (8)

1 (10)

Cancer site n (%)

 Breast

24 (24)

2 (20)

 Hematological

22 (22)

3 (30)

 Urological

14 (14)

2 (20)

 Lung

13 (13)

0 (0)

 Gynecological

11 (11)

2 (20)

 Head and neck

10 (10)

1 (10)

 Gastrointestinal

8 (8)

0 (0)

 Brain

4 (4)

0 (0)

 Skin

2 (2)

0 (0)

Performance statusc

 Karnofsky Performance Scale Index

  90–100

17 (17)

2 (20)

  60–89

20 (20)

3 (30)

  < 60

3 (3)

0 (0)

  Missing %

60 (60)

5 (50)

 Country n (%)

  The Netherlands

60 (60)

5 (50)

  Dutch-speaking Belgium

40 (40)

5 (50)

  1. a In Round 2, a subset of participants (n = 5) from Belgium were re-interviewed and five new participants were recruited in the Netherlands
  2. bSome participants received more than one treatment type
  3. c Performance status was only captured in the Belgian sample