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Table 1 Patients’ characteristics

From: A change from gonadotropin releasing hormone antagonist to gonadotropin releasing hormone agonist therapy does not affect the oncological outcomes in hormone sensitive prostate cancer

  

Degarelix (Continued group)

Conversion from degarelix to GnRH agonist (Changed group)

p value

Number of patients

  

51

 

57

 

Follow up duration (months)

median (range)

19.4

(1.0–57.9)

38.8

(2.2–58.6)

< 0.001

Degarelix treatment duration (months)

median (range)

14

(1–52)

8

(1–39)

0.064

Age (years)

median (range)

73

(49–95)

75

(50–90)

0.572

T stage

T1

3

5.9%

1

1.8%

0.387

T2

10

19.6%

18

31.6%

T3

24

47.1%

26

45.6%

T4

14

27.4%

12

21.1%

N

N0

29

56.9%

31

54.4%

0.796

N1

22

43.1%

26

45.6%

M

M0

16

31.4%

23

40.4%

0.486

M1

35

68.6%

34

59.6%

Gleason score

6

1

2.0%

2

3.5%

0.389

7

5

9.8%

6

10.5%

8

21

41.2%

24

42.1%

9

15

29.4%

15

26.3%

10

4

7.8%

5

8.8%

unknown

5

9.8%

5

8.8%

 

Initial PSA (ng/ml)

Median (range)

145

(0.48–8072)

122

(5.62–9675)

0.669

PSA

PSA 0–4

1

2.0%

0

0.0%

0.415

PSA4–10

5

9.8%

3

5.3%

PSA10–20

2

3.9%

5

8.8%

PSA > 20

43

84.3%

49

86.0%

Treatment

CAB

48

94.1%

54

94.7%

0.889

GnRH only

3

5.9%

3

5.3%

Transition to CRPC

No

37

72.5%

38

66.7%

0.508

Yes

14

27.5%

19

33.3%

% PSA decrease by degarelix

median (range)

−99.4%

(6.6–100.0)

−99.8%

(47.2–100.0)

0.068

  1. Abbreviations CAB combined androgen blockade, CRPC castration resistant prostate cancer, GnRH gonadotropin releasing hormone