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Table 1 Baseline demographic and disease characteristics

From: Efficacy and safety of lanreotide autogel compared with lanreotide 40 mg prolonged release in Chinese patients with active acromegaly: results from a phase 3, prospective, randomized, and open-label study (LANTERN)

 

Lanreotide autogel

(N = 64)

Lanreotide 40 mg PR (N = 64)

All patients

(N = 128)

Age, years

 Mean (SD)

37.9 (11.2)

40.8 (12.6)

39.4 (11.9)

Sex, n (%)

 Male

26 (40.6)

24 (37.5)

50 (39.1)

 Female

38 (59.4)

40 (62.5)

78 (60.9)

BMI, kg/m2

 Mean (SD)

26.3 (3.6)

26.1 (3.6)

26.2 (3.6)

Time since acromegaly, years

 Mean (SD)

3.70 (5.83)

3.14 (4.09)

3.42 (5.02)

Previous treatment, n (%)

 Pituitary surgery

44 (68.8)

44 (68.8)

88 (68.8)

 Radiotherapy

3 (4.7)

3 (4.7)

6 (4.7)

Any acromegaly medication ≤ 6 months prior to study entry, n (%)

10 (15.6)

12 (18.8)

22 (17.2)

Tumor assessment at baseline by central evaluation, n (%)

(n = 63)

(n = 64)

(n = 127)

 Microadenomaa

15 (23.4)

12 (18.8)

27 (21.1)

 Macroadenomaa

43 (67.2)

47 (73.4)

90 (70.3)

 No tumor

5 (7.8)

5 (7.8)

10 (7.8)b

Solid component (μL)

(n = 58)

(n = 57)

(n = 115)

 Mean (SD)

4990.5 (8752.8)

2589.1 (2666.5)

3800.2 (6576.7)

  1. Data are presented from the intention-to-treat population. aTumor diameters: ≤10 mm were classified as microadenomas and > 10 mm as macroadenomas. bPatients who had no tumors at baseline had GH levels ranging from 3.3–24.3 μg/L in the lanreotide autogel group (n = 5), and 2.8–13.0 μg/L in the lanreotide 40 mg PR group (n = 5). BMI body mass index, GH growth hormone, PR prolonged release, SD standard deviation