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. 2023 Mar 4;23:206. doi: 10.1186/s12885-023-10676-x

Table 2.

Clinical efficacy and improvements in CNS-related symptoms in the study population

BM cohort
(N = 12)
N(%)
LM cohort
(N = 16)
N(%)
Median follow up duration
 Month (range) 6.3 (1.5–15.1) 7.8 (1.9–15.4)
Median iPFS, months (95%CI) 3.6 (1.435–5.705) 4.3 (2.094–6.486)
Median PFS, months (95%CI) 2.3 (0.000–4.677) 4.3 (2.094–6.486)
Overall best intracranial response
 ORR 2 (22.2)
 DCR 8 (88.9)
 CR 0 (0.0)
 PR 2 (22.2)
 SD 6 (66.7)
 PD 1 (11.1)
 Not evaluable 3 (25.0)
Overall best extracranial response
 ORR 1 (8.3) 1 (6.3)
 DCR 4 (33.3) 7 (43.8)
 CR 0 (0.0) 0 (0.0)
 PR 1 (8.3) 1 (6.3)
 SD 3 (25.0) 6 (37.5)
 PD 4 (33.3) 1 (6.3)
 Not evaluable 4 (33.3) 8 (50.0)
Number of OS events (%) 4 (33.3) 7 (43.8)
Number of PFS events (%) 12 (100.0) 9 (56.3)
Number of iPFS events (%) 10 (83.3) 9 (56.3)
Improvement in CNS-related symptoms
 Improvement 3 (100.0) 8 (53.3)
 No improvement 0 (0.0) 4 (26.7)
 Deterioration in symptoms 0 (0.0) 3 (20.0)

The percentages might not equal 100% on account of rounding

n number, CNS central nervous system, iPFS intracranial progression-free survival, PFS progression-free survival, CR complete remission, PR partial response, SD stable disease, PD progressive disease, ORR objective response rate (ORR = CR + PR), DCR disease control rate (DCR = CR + PR+ SD)