Table 2 Subgroup analysis of efficacy endpoints

From: Comparative analysis of ctDNA monitoring strategies in advanced NSCLC with MET exon 14 skipping mutations treated with ensartinib

Subgroups

MET-specific alterations

Canonical alterations

Pan-alterations

ctDNA Negative

ctDNA Positive

ctDNA Negative

ctDNA Positive

ctDNA Negative

ctDNA Positive

V0

 Rate

51.7%

48.3%

51.7%

48.3%

24.1%

75.9%

 ORR (95% CI)

60.0% (35.2–84.8%)

50.0% (23.0–77.0%)

60.0% (35.2–84.8%)

50.0% (23.0–77.0%)

71.4% (29.0–96.3%)

50.0%(28.2–71.8%)

 mPFS, m (95% CI)

7.5 (6.0–20.2)

4.9 (2.2-NA)

7.5 (6.0–20.2)

4.9 (2.2-NA)

7.7 (6.0-NA)

6.0 (3.0–9.2)

 mOS, m (95% CI)

27.6 (11.8-NA)

9.5 (8.2-NA)

27.6 (11.8-NA)

9.5 (8.2-NA)

NA (16.3-NA)

27.6 (8.2-NA)

V1

 Rate

70.0%

30.0%

75.0%

25.0%

34.5%

65.5%

 ORR (95% CI)

64.3% (35.1–87.2%)

16.7% (4.0–64.1%)

60.0% (35.2–84.8%)

20.0% (5–71.6%)

71.4% (29.0–96.3%)

38.5% (13.9–68.4%)

 mPFS, m (95% CI)

7.9 (6.0-NA)

2.2 (2.2-NA)

7.9 (6.0-NA)

2.2 (2.2-NA)

8.2 (4.1-NA)

6.0 (3.0-NA)

 mOS, m (95% CI)

16.3 (9.2-NA)

NA (7.8-NA)

16.3 (9.2-NA)

NA (7.8-NA)

16.3 (6.3-NA)

NA (9.2-NA)

Longitudinal Pan-mutation Dynamics

mPFS for ctDNA Negative, m (95% CI)

6.8 (5.9-NA)

6.8 (5.9-NA)

7.1 (6.0-NA)

mPFS for ctDNA Residual, m (95% CI)

2.2 (2.2-NA)

2.2 (2.2-NA)

5.9 (3.0–6.0)

mPFS for ctDNA Clearance, m (95% CI)

9.3 (6.0-NA)

9.3 (6.0-NA)

8.5 (4.1-NA)

  1. ctDNA circulating tumor DNA, V0 baseline, V1 4 weeks after treatment initiation, ORR objective response rate, mPFS median progression-free survival, mOS median overall survival, NA not available.