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Table 2 Overview of duration of treatment and TEAE profile across cohorts

From: Phase 1 study of M2698, a p70S6K/AKT dual inhibitor, in patients with advanced cancer

 

M2698 monotherapy (N = 62)

M2698/trastuzumab (N = 13)

M2698/tamoxifen (N = 26)

Duration of M2698 therapy

≤ 6 weeks

26 (41.9)

6 (46.2)

10 (38.5)

> 6–12 weeks

16 (25.8)

1 (7.7)

5 (19.2)

> 12 weeks

20 (32.3)

6 (46.2)

11 (42.3)

Median, weeks (range)

7.4 (0.86–72.0)

6.9 (2.0–35.9)

8.4 (0.1–105.1)

TEAEs

61 (98.4%)

13 (100.0)

25 (96.2)

TEAEs, grade ≥ 3

36 (58.1%)

9 (69.2)

15 (57.7)

TEAE related to M2698

34 (54.8%)

10 (76.9)

22 (84.6)

TEAE related to M2698, grade ≥ 3

8 (12.9%)

3 (23.1)

5 (19.2)

TEAE l/t permanent discontinuation of any trial treatment

6 (9.7%)

3 (23.1)

9 (34.6)

TEAE l/t temporary discontinuation of M2698

29 (46.8%)

6 (46.2)

11 (42.3)

Serious TEAEs

26 (41.9)

5 (38.5)

13 (50.0)

Serious TEAE related to M2698

5 (8.1)

1 (7.7)

3 (11.5)

TEAE leading to deatha

6 (9.7)

2 (15.4)

3 (11.5)

  1. Data are presented as number of patients (percent) unless otherwise stated
  2. l/t leading to, TEAE = treatment-emergent adverse event
  3. aNo deaths were considered to be related to M2698, trastuzumab or tamoxifen. Primary causes of death included disease progression, TEAEs not related to study drug or procedures, unknown reasons and disease related