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Table 4 Patients’ presentation and reported outcomes at baseline by treatment strategy, N (%)

From: The diffuse-type tenosynovial giant cell tumor (dt-TGCT) patient journey: a prospective multicenter study

 

Wait and See (n = 81)

Surgery only (n = 41)

Systemic only (n = 37)

Mean age [years] ± SD

44.3 ± 15.17

41.8 ± 14.94

47.7 ± 10.44

Time since diagnosis primary tumor

[months] median (Q1, Q3)

34.3

(13.8–77.9)

6.7

(1.2–59.8)

32.1

(18.2–89.6)

Treatment before baseline

   

 Therapy-naïve

11 (13.6)

16 (39.0)

–

 Surgery only

47 (58.0)

20 (48.8)

7 (18.9)

 Systemic only

2 (2.5)

–

9 (24.3)

 Multimodal treatment

21 (25.9)

5 (12.2)

21 (56.8)

Admission status

   

 Primary diagnosis

47 (58.0)

27 (65.9)

19 (51.4)

 Recurrent diseases

34 (42.0)

14 (34.1)

18 (48.6)

Indication MRI closest to baseline

   

 Primary diagnosis

7 (9.3)

23 (57.5)

4 (11.4)

 Pre-surgery

5 (6.7)

8 (20.0)

2 (5.7)

 Regular postoperative follow-up

43 (57.3)

6 (15.0)

7 (20.0)

 Follow-up due to complaints

15 (20.0)

2 (5.0)

13 (37.1)

Severity

   

 Moderate

34 (42.0)

15 (36.6)

12 (32.4)

 Severe

38 (46.9)

20 (48.8)

21 (56.8)

 Not assessable

9 (11.1)

6 (14.6)

4 (10.8)

In last 24 months prior to baseline

   

 Any rehabilitation

17 (26.2)

5 (13.2)

4 (12.5)

 Specialist visitsa,

 Median (range)

5.0

(1.0–70.0)

3.0

(10–27.0)

12

(2.0–65.0)

 Physical therapy sessionsa,

 Median (range)

18.0

(4.0–200.0)

11.0

(1.0–100.0)

11.5

(3.0–90.0)

Symptoms

   

 Pain

56 (69.1)

37 (90.2)

32 (86.5)

 Stiffness

36 (44.4)

27 (65.9)

23 (62.2)

 Swelling

44 (54.3)

34 (82.9)

19 (51.4)

 Limited range of motion

39 (48.1)

31 (75.6)

30 (81.1)

 ≥ 3 symptoms

31 (38.3)

28 (68.3)

22 (59.5)

Analgesics use

8 (9.9)

5 (12.2)

9 (24.3)

Worst stiffness NRS

Mean ± SD (n = 144)

3.4 ± 2.57

5.2 ± 3.14

5.3 ± 2.55

Worst pain NRS

Mean ± SD (n = 81)

5.0 ± 2.41

6.5 ± 2.27

5.8 ± 1.97

Pain severity score

Median (Q1, Q3) (n = 147)

2.25

(0.75–4.00)

4.25

(1.50–6.25)

4.25

(1.50–5.50)

Pain interference score

Median (Q1, Q3) (n = 146)

1.57

(0.14–4.00)

3.00

(1.14–5.57)

3.00

(0.57–5.57)

PROMIS-PF

Median (Q1, Q3) (n = 142)

44.43

(37.30–49.29)

39.54

(34.95–44.42)

39.98

(34.79–43.69)

EQ-5D Index score

Median (Q1, Q3) (n = 153)

0.84

(0.67–0.89)

0.80

(0.53–0.84)

0.74

(0.48–0.84)

EQ-5D VAS

Median (Q1, Q3) (n = 154)

79.0

(60.0–85.0)

69.0

(60.0–80.0)

70.0

(50.0–75.0)

  1. EQ-5D EuroQol 5D, MRI magnetic resonance imaging, NRS numeric rating scale, PROMIS Patient-Reported Outcomes Measurement Information System; PROMIS-PF Patient-Reported Outcome Measurement Information System Physical Functioning®, Q1 quarter 1, Q3 quarter 3, SD standard deviation, VAS visual analog scale
  2. aBased on patients that had any