Journal of Clinical Oncology, Vol 4, 68-73, Copyright © 1986 by American Society of Clinical Oncology
Combination intraventricular chemotherapy for meningeal neoplasia
L Giannone, FA Greco and JD Hainsworth
Twenty two patients with meningeal neoplasia were treated with biweekly
combination intraventricular chemotherapy using methotrexate, cytosine
arabinoside, and thiotepa. Patients with the following malignancies were
included: breast cancer, ten patients; lung cancer, seven; non- Hodgkin's
lymphoma, two; malignant melanoma, one; transitional cell carcinoma of the
bladder, one; and malignant glioma, one. Eight of 22 patients (36%) had a
Karnofsky performance status of less than 50%. Eleven of 22 patients
received radiotherapy to symptomatic areas, and seven received systemic
chemotherapy in addition to combination intraventricular therapy. Patients
were evaluated for both toxicity and response to therapy. Myelosuppression
was the major toxic condition and occurred in 17 of 22 patients (77%). Ten
patients (45%) had a nadir WBC count of less than 1000/microL or a platelet
count of less than 25,000/microL. No patient achieved a complete response
(CR), although nine patients (41%) had partial responses (PRs) lasting 4 to
24 + weeks. Median survival for the entire group was 10 weeks (range, 6 to
24+ weeks). In this small group of patients, simultaneous triple-drug
intraventricular chemotherapy caused unacceptable myelosuppression without
increasing the response rate, response duration, or survival when compared
with single-agent methotrexate and radiotherapy.

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