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. 2021 Oct 20;71(6):1393–1402. doi: 10.1007/s00262-021-03091-3

Table 2.

Summary of key efficacy results

Cohorts by PD-L1 expression All patients (n = 146)
 < 1% (n = 74)  ≥ 1–< 25% (n = 31)  ≥ 25–< 50% (n = 11)  ≥ 50%
Total (n = 30) EGFR − (n = 25) EGFR + (n = 5)
Best overall response, n (%)
 PR 9 (12.2) 6 (19.4) 4 (36.4) 7 (23.3) 7 (28.0) 0 26 (17.8)
 SD 24 (32.4) 10 (32.3) 5 (45.5) 12 (40.0) 10 (40.0) 2 (40.0) 51 (34.9)
 PD 33 (44.6) 13 (41.9) 1 (9.1) 7 (23.3) 6 (24.0) 1 (20.0) 54 (37.0)
 NE 8 (10.8) 2 (6.5) 1 (9.1) 4 (13.3) 2 (8.0) 2 (40.0) 15 (10.3)
Objective response rate, % (95% CI) 12.2 (5.7–21.8) 19.4 (7.5–37.5) 36.4 (10.9–69.2) 23.3 (9.9–42.3) 28.0 (12.1–49.4) 0 17.8 (12.0–25.0)
Disease control rate, % (95% CI) 44.6 (33.0–56.6) 51.6 (33.1–69.8) 81.8 (48.2–97.7) 63.3 (43.9–80.1) 68.0 (46.5–85.1) 40.0 (5.3–85.3) 52.7 (44.3–61.1)
Duration of response, months (95% CI) 8.3 (3.8–22.3) 27.1 (5.6–NE) NR (2.8–NE) 15.1 (2.8–NE) 15.1 (2.8–NE) NR 13.6 (5.6–22.6)

PR partial response, SD stable disease, PD progressive disease, NE not estimable, NR not reached