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A Phase II trial of intra-cerebrospinal fluid alpha interferon in the treatment of neoplastic meningitis

โœ Scribed by Marc C. Chamberlain


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
64 KB
Volume
94
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


Abstract

BACKGROUND

Neoplastic meningitis (NM), a metastatic complication of both primary central nervous system and systemic cancer, occurs in 1โ€5% of patients with known cancer. Currently available treatment options are limited and provide only modest benefit. The current study was performed to determine the toxicity and response rate of intraโ€cerebrospinal fluid (CSF) alpha interferon (ฮฑโ€IFN) in the treatment of patients with NM.

METHODS

Twenty two patients (median age, 56 years) with clinical and cytologically documented NM received intraโ€CSF ฮฑโ€IFN. Tumor histologies included: lung (five patients); brain (five patients); nonโ€Hodgkin lymphoma (three patients); breast (three patients); melanoma (two patients); chronic myelogenous leukemia (two patients); colon (one patient); and prostate (one patient). Concurrent involvedโ€field radiotherapy (12 out of 22 patients) or systemic chemotherapy (11 out of 22) was administered based on clinical indications. โ€ฮฑโ€IFN was administered at a fixed dose (1 ร— 10^6^ IU every other day given three times per week for four weeks by induction). Patients were evaluated by CSF cytology and neurologic examination at the conclusion of induction therapy. Responding patients continued to receive ฮฑโ€IFN with monthly evaluations.

RESULTS

Ten out of 22 patients (45%) treated with ฮฑโ€IFN had a cytologic response and either stable or improved neurologic status at the conclusion of induction. Duration of response ranged from 8 to 40 weeks (median, 16 weeks). Toxicity was manifested as transient chemical arachnoiditis (16 out of 22 patients; 60% of all treatment cycles) and chronic fatigue (20 out of 22 patients). No treatmentโ€related hospitalizations or deaths were seen.

CONCLUSIONS

ฮฑโ€IFN has modest activity against NM. However, it is associated with considerable toxicity at the dose and schedule used in the current study and, as a result, may prove difficult to administer. Cancer 2002;94:2675โ€“80. ยฉ 2002 American Cancer Society.

DOI 10.1002/cncr.10547


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