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. 2023 Nov 27;24:100331. doi: 10.1016/j.lansea.2023.100331

Table 1.

Baseline details of the participants.

Variable Value (N = 84)
Age in years-No (%)
 Median (Range) 52.5 (21–75)
 Non-Elderly 61 (72.6)
 Elderlyb 23 (27.4)
Gender-No (%)
 Male 38 (45.2)
 Female 46 (54.8)
ECOG PS-No (%)
 1 41 (48.8)
 2 28 (33.3)
 3 9 (10.7)
 4 6 (7.1)
Disease site-No (%)
 Breast 22 (26.2)
 Lung (NSCLC) 45 (53.6)
 Lung (SCLC) 1 (1.2)
 Gastrointestinal 9 (10.7)
 Others 7 (8.3)
NSCLC-Molecular types-No (%)a
 EGFR mutation 36 (42.9)
 ALK rearrangement 3 (3.6)
 No mutation 7 (8.3)
Breast cancer-Molecular types-No (%)a
 TNBC 11 (13.1)
 ER/PR+ & Her-2 negative 9 (10.7)
 ER/PR- & Her-2 positive 1 (1.2)
 ER/PR- & Her-2 positive 1 (1.2)
Number prior therapies-No (%)
 Nil 2 (2.4)
 1 43 (51.2)
 2 20 (23.8)
 3 15 (17.9)
 ≥4 4 (4.8)
LMC diagnosis-No (%)
 Confirmed 52 (61.9)
 Probable 32 (38.1)
Extracranial disease status at diagnosis-No (%)
 Progressive disease 39 (46.4)
 Stable disease 31 (36.9)
 Partial response 8 (9.5)
 Complete response 5 (6)
 Missing data 1 (1.2)

ECOG PS- Eastern Cooperative Oncology Group Performance Status. NSCLC- Non small cell lung cancer, SCLC–small cell lung cancer, EGFR-epidermal growth factor receptor, ALK- Anaplastic lymphoma kinase, ER-Estrogen receptor, PR-Progesterone receptor, Her-2-human epidermal growth factor receptor 2, LMC-Leptomeningeal carcinomatosis.

a

Restrict to 22 patients with breast cancer and 45 patients with NSCLC.

b

‘Elderly’ was defined as age >60 years.