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. Author manuscript; available in PMC: 2017 Aug 30.
Published in final edited form as: Int J Radiat Oncol Biol Phys. 2016 Jun 14;96(2):406–413. doi: 10.1016/j.ijrobp.2016.06.006

Table 2.

Median survival and time from primary diagnosis to brain metastasis by gene status and tyrosine kinase inhibition

Factor n (%) MS, mo IQR, mo P values vs EGFR & ALK−;* vs no TKI Mean time: primary diagnosis to BM, mo P value vs EGFR & ALK
Adenocarcinoma overall 1521 15 14–17 16
 Alteration status unknown 705 (46) 12 5–25 .12* 19 .08
 Alteration status known 816 (54) 19 7–40 13
EGFR & ALK 284 (35) 14 10 ref* 10 ref
EGFR+ 235 (29) 23 20–28 <.01* 15 .02
  No TKI before BM 161 (69) 30 12–47 ref
  Received TKI before BM 74 (31) 17 9–26 <.01
ALK+ 86 (10) 45 32–62 <.01* 20 <.01
  No TKI before BM 53 (61) 45 31-NR ref
  Received TKI before BM 33 (39) NR 5-NR .43
KRAS+ 211 (26) 12 5–32 .84* 13 .25

Abbreviations: MS = median survival; NR = not reached; ref = reference; TKI = tyrosine kinase inhibition.

Percentages (%) are within the subgroup whose total is above and 1 column left. For example, 211/816 = 26% of patients with known alterations were KRAS+, and 161/235 = 69% of patients who were EGFR+ did not receive TKI before BM.

Forty-five patients had invalid dates and were excluded for metastasis time evaluation.

*

P values are from log-rank tests comparing survival distributions between each alteration group—EGFR+, ALK+, KRAS+, and unknown—and the EFGR & ALK− group as reference.

P values are from log-rank tests comparing survival distributions between each TKI group, within EGFR+ and ALK+ subgroups, respectively.

P values are from Wilcoxon rank sum tests comparing the time from primary diagnosis to BM between each alteration group and the EGFR & ALK− group as reference. TKI could be initiated at any time between primary diagnosis and BM, so time from primary diagnosis to BM was compared for TKI with time-dependent analyses (results not presented in table).