Table 1 Demographic and clinicopathological characteristics of the study population

From: PPP2R1A mutations portend improved survival after cancer immunotherapy

Characteristics

Mutated PPP2R1A (n = 11)

Wild-type PPP2R1A (n = 23)

P

Age at consent, median (range)

55.0 (46.0–72.0)

57.0 (36.0–78.0)

0.954a

Arm of trial, n (%)

  

0.529

NCT03026062

  

Sequential

1 (9.1)

4 (17.4)

Combination

9 (81.8)

19 (82.6)

NCT01928394

  

Combination

1 (9.1)

0 (0.0)

Previous lines of therapy, median (range)

2.0 (1.0–8.0)

2.0 (1.0–9.0)

0.938b

Platinum response, n (%)

  

1.000

Platinum resistant

10 (90.9)

20 (87.0)

Platinum refractory

1 (9.1)

3 (13.0)

Race, n (%)

  

0.577

White

8 (72.7)

19 (82.6)

Asian

3 (27.3)

3 (13.0)

Other

0 (0.0)

1 (4.3)

BRCA status, n (%)

  

0.324

Somatic mutation (BRCA1)

1 (9.1)

0 (0.0)

Wild type

10 (90.9)

23 (100.0)

Microsatellite stability status, n (%)

  

0.549

MSIhigh

0 (0.0)

1 (4.3)

MSS

10 (90.9)

22 (95.7)

Unknown

1 (9.1)

0 (0.0)

PD-L1 status, n (%)

  

0.114

Positive

3 (27.3)

13 (56.5)

Negative

4 (36.4)

8 (34.8)

Unknown

4 (36.4)

2 (8.7)

AKT alteration present, n (%)

  

0.280

Yes

0 (0.0)

4 (17.4)

No

11 (100.0)

19 (82.6)

ARID1A mutation present, n (%)

  

0.682

Yes

9 (81.8)

16 (69.6)

No

2 (18.2)

7 (30.4)

PIK3CA mutation present, n (%)

  

0.717

Yes

5 (45.5)

13 (56.5)

No

6 (54.5)

10 (43.5)

Grade 3 or higher irAE

  

0.079

No grade 3 or higher irAE

6 (54.5)

20 (87.0)

Any grade 3 or higher irAE

5 (45.5)

3 (13.0)

  1. irAE, immune-related adverse events; MSS, microsatellite stable. Except where indicated, P values were calculated using Fisher’s exact tests. All P values reported are two-sided.
  2. aP value was calculated using a Student’s t-test.
  3. bP value was calculated using a Wilcoxon rank-sum test.