Mc. Chamberlain et P. Kormanik, LEPTOMENINGEAL METASTASES DUE TO MELANOMA - COMBINED-MODALITY THERAPY, International journal of oncology, 9(3), 1996, pp. 505-510
A Phase II study of combined modality therapy of leptomeningeal metast
ases (LM) in melanoma was carried out. Central nervous system (CNS) me
tastases occur commonly in patients with clinically advanced melanoma.
16 patients (median age 47; range 32-62 years) with LM due to metasta
tic melanoma were treated. Neurologic presentation included: headache
(9 patients); cranial neuropathies (6); cauda equina syndrome (4); gai
t ataxia (3); hemiparesis (2); radiculopathy (2); myelopathy (1); and
seizure (1). All patients underwent CNS staging followed by radiothera
py (14 patients) and intraventricular chemotherapy (methotrexate 16 pa
tients; ara-C 13 patients; thio-TEPA 7 patients). CNS imaging demonstr
ated: interrupted CSF flow (9 patients); parenchymal brain metastases
(7); spinal cord subarachnoid nodules (5); hydrocephalus (3); and epid
ural spinal cord compression (2). CSF cytologic responses were seen in
4 patients to first-, 6 to second-, and 3 to third-line chemotherapy.
Treatment-related toxicity included 13 patients with meningitis (12 c
hemical; 1 bacterial) and 12 patients (18 episodes) with myelosupressi
on (4 episodes secondary to intraventricular chemotherapy). Median sur
vival was 4 months (range: 2-8). Twelve patients (75%) died of progres
sive LM or combined LM and systemic disease progression. LM in patient
s with metastatic melanoma may be palliated with combined modality the
rapy, however, median survival is quite short suggesting a re-evaluati
on of such an approach in similarly affected patients.