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. 2024 Jan 22;11(3):710–718. doi: 10.1002/acn3.51991

Table 1.

Characteristics of the study sample.

Total (N = 27)
Age at symptom onset (median [Q1, Q3], years) 65.0 [54.0, 71.0]
Male sex (n, %) 12/27 (44.4)
White ethnicity (n, %) 26/27 (96.3)
Follow‐up time from symptom onset (median [Q1, Q3], months) 53.9 [11.2, 102.2]
Cancer (n, %) 15/27 (55.6)
SCLC (n, %) 8/15 (53.3)
Thymoma (n, %) 4/15 (26.7)
Other (n, %) 3/15 (20.0)
Without cancer (n, %) 12/27 (44.4)
Pulmonary nodules 1 (n, %) 7/12 (58.3)
Smoking history (n, %) 22/27 (81.5)
CSF with inflammation 1 (n, %) 9/11 (81.8)
Deceased (n, %) 13/27 (48.1)
Due to cancer (n, %) 5/13 (38.5)
Due to neurologic cause (n, %) 1/13 (7.7)
Other causes (n, %) 7/13 (53.8)
Received immunotherapy (n, %) 15/27 (55.6)
Acute immunotherapy (IVMP, IVIG or PLEX) (n, %) 11/15 (73.3)
Cyclophosphamide (n, %) 3/15 (20.0)
Mycophenolate mofetil (n, %) 1/15 (6.7)
Other (n, %) 4/15 (26.7)
Wheelchair dependence due to PND (n, %) 10/27 (37.0)
mRS at first visit (median [Q1, Q3]) 2.0 [2.0, 3.0]
Moderate–severe mRS at first visit (mRS 3–5) (n, %) 11/27 (40.7)
mRS at last visit (median [Q1, Q3]) 3.0 [2.0, 4.0]
Moderate–severe mRS at last visit (mRS 3–5) (n, %) 18/27 (66.7)
Clinical phenotypes
Cerebellar ataxia (n, %) 11/27 (40.7)
Myelopathy (n, %) 8/27 (29.6)
Polyneuropathy/radiculopathy (n, %) 14/27 (51.9)
Myasthenia (n, %) 7/27 (25.9)
Autoimmune encephalopathy (n, %) 7/27 (25.9)
Optic neuropathy (n, %) 6/27 (22.2)

Statistics presented as median [P25, P75], N (column %).

Abbreviations: SCLC, small cell lung cancer; CSF, cerebrospinal fluid; MRI, magnetic resonance imaging; IVMP, intravenous methylprednisolone; IVIG, intravenous immunoglobulin; PLEX, plasma exchange; mRS, modified Rankin Scale.

1

Data are not available for all subjects. Missing values: Pulmonary nodules = 4; CSF = 16.