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. Author manuscript; available in PMC: 2020 Sep 1.
Published in final edited form as: Lancet Oncol. 2019 Dec 11;21(2):271–282. doi: 10.1016/S1470-2045(19)30691-6

Table 2:

Activity outcomes

Efficacy-evaluable population* (n=54) Patients with baseline CNS disease (n=12) Patients with no baseline CNS disease* (n=42)
Proportion of patients achieving a response 31 (57%) 6 (50%) 25 (60%)
Best overall response
 Complete response 4 (7%) 0 4 (10%)
 Partial response 27 (50%) 6 (50%) 21 (50%)
 Stable disease 9 (17%) 4 (33%) 5 (12%)
 Progressive disease 4 (7%) 0 4 (10%)
 Non-complete response or progressive disease 3 (6%) 0 3 (7%)
 Missing or unevaluable 7 (13%) 2 (17%) 5 (12%)
Median duration of response, months 10·4 (7·1-NE) NE 12·9 (7·1-NE)
Median progression-free survival, months 11·2 (8·0–14·9) 7·7 (4·7-NE) 12·0 (8·7–15·7)

Data are n (%) or median (95% CI). NE=not estimable.

*

Systemic response.

CNS disease status determined by the investigator.

Missing or unevaluable included patients with no post-baseline scans available, missing subsets of scans at all time points, or patients who discontinued before obtaining adequate scans to evaluate or confirm response.