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. 2022 Aug 18;7(5):100562. doi: 10.1016/j.esmoop.2022.100562

Table 3.

Summary of response rates: all-treated population

EOC (n = 18) GBM (n = 33) HCC (n = 27) SCCHN (n = 29) Overalla (n = 74)
Best overall response, n (%)
 Complete responseb 0 0 0 1 (3.4) 1 (1.4)
 Partial responseb 1 (5.6) 0 2 (7.4) 3 (10.3) 6 (8.1)
 Stable disease 6 (36.3) 4 (12.1) 8 (29.6) 7 (24.1) 21 (28.4)
 Progressive disease 10 (55.6) 26 (78.8) 14 (51.9) 11 (37.9) 35 (47.3)
 Not assessablec 1 (5.6) 3 (9.1) 3 (11.1) 7 (24.1) 11 (14.9)
 Unconfirmed complete response 1 (5.6) 0 0 1 (1.4)
 Unconfirmed partial response 0 1 (3.7) 0 1 (1.4)
Overall response, n (%)
 Responders (complete or partial response)b 1 (5.6) 0 2 (7.4) 4 (13.8) 7 (9.5)
 90% CId 0.3-23.8 0.0-8.7 1.3-21.5 4.9-28.8 4.5-17.0
Median PFS (95% CI) 2.04 (1.91-3.94) 1.30 (1.22-1.38) 2.04 (1.84-4.01) 2.10 (1.84-1.91) 1.92 (1.81-2.04)e

CI, confidence interval; EOC, epithelial ovarian cancer; GBM, glioblastoma; HCC, hepatocellular carcinoma; PFS, progression-free survival; SCCHN, squamous cell carcinoma of the head and neck.

a

Including EOC, HCC, and SCCHN cohorts, as per RECIST v1.1 criteria.

b

Confirmation of response was required.

c

Including patients with no target and non-target lesions identified at baseline and no new lesions reported in post-baseline tumor assessments, or patients with only non-target lesions identified at baseline with non-complete response/non-progressive disease reported for non-target lesion and no new lesions reported in post-baseline tumor assessments.

d

Estimated using the Clopper–Pearson method.

e

PFS estimate for all-treated population (n = 107).