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. Author manuscript; available in PMC: 2018 Feb 1.
Published in final edited form as: Clin Breast Cancer. 2016 Jul 25;17(1):23–28. doi: 10.1016/j.clbc.2016.07.002

Table 1.

Patient characteristics (N=318)

Characteristics N % Univariate
association
with OS
Age at LM diagnosis (years) Median 54
Range 23–84

Age at BC diagnosis (years) Median 46.4
Range 20.5–77.4

Time from MBC to LM
diagnosis (months)
Median 22.6
Range 0–238

Year of LM diagnosis 1998 – 2005 98 31% < 0.01
2006 – 2013 220 69%

Receptor status HR+/HER2− 140 44% <0.01
HR any/ HER2+ 83 26%
HR− / HER2− 81 26%
Missing 14 4%

KPS at LM diagnosis < 70 58 18% <0.01
≥ 70 223 70%
Missing 37 12%

Stage at the time of initial BC
diagnosis
I 26 8%
II 68 21%
III 40 13%
IV 78 25%
Missing 106 33%

Grade of primary BC I/II 36 11% 0.06
III 199 63%
Missing 83 26%

Method of LM diagnosis
confirmation
Cytology and imaging 95 30%
Cytology only 12 4%
Imaging only 208 65%
Clinical* 3 1%

Sites of LM involvement Cranial only 135 43% 0.04
Spine only 84 26%
Cranial and spine 83 26%
Missing 16 5%

Non- CNS disease control
status
NED 34 11% 0.002
Non-POD 102 32%
POD 168 53%
Missing 14 4%

Presence of brain metastases Prior to LMD diagnosis 139 44% 0.007
Concurrent with LMD diagnosis 69 22%
After LMD diagnosis 8 3%
No 102 32%

LM specific treatment Radiation 203 64%
Intrathecal/ventricular therapy 46 14%
IV therapy (HD methotrexate) 64 20%
VP shunt placement 60 19%

Systemic therapy use after LM
diagnosis
No 126 40% <0.001
Yes 192 60%
*

No information on imaging or cytology was available but patients were documented to have LM diagnosis and treated with LM specific treatment.

Abbreviations: N, sample size, LMD, leptomeningeal disease; BC, breast cancer; MBC, metastatic breast cancer; KPS, Karnofsky Performance Status; CNS, central nervous system; HR, hormone receptor; NED, no evidence of disease; Non-POD, non-progressing disease; POD, progressive disease; IV, intravenous; HD, high dose; VP, ventriculoperitoneal