Journal of Clinical Oncology, Vol 2, 359-364, Copyright © 1984 by American Society of Clinical Oncology
Treatment of meningeal relapse in childhood acute lymphoblastic leukemia. I. Results of craniospinal irradiation
LE Kun, BM Camitta, RK Mulhern, SJ Lauer, RW Kline, JT Casper, BA Kamen, BM Kaplan and SW Barber
Fourteen children were treated for isolated meningeal relapse occurring
seven to 44 months (median, 14 months) after prophylactic cranial
irradiation (2,400 rad/12 fractions) and intrathecal methotrexate (IT MTX,
12 mg/m2 for four doses during cranial irradiation). Eight had "high-risk"
acute lymphocytic leukemia with age less than 2 years, white blood cell
counts greater than 20,000, or T cell markers. Treatment for central
nervous system leukemia included IT MTX (12 mg/m2 twice weekly until
clearance of spinal fluid cytology) followed by craniospinal irradiation
(CSI, 3,000 rad/20 fractions to the cranium and 1,800 rad/12 fractions to
the spine). No maintenance IT MTX was given. Systemic chemotherapy was
continued or reinstituted for a minimum of one year after CSI. No instance
of second meningeal relapse has occurred. Five patients remain in secondary
complete remission 66+, 54+, 36+, 26+, and 24+ months after meningeal
relapse. Disease-free survival was limited by marrow relapse in eight
patients (2-20 months after CSI) and testicular relapse in one. No acute
toxicities were noted with CSI. Myelosuppression occurred in seven
patients. Infections within two months of CSI were noted in five. No
neurologic sequelae are apparent. Serial neuropsychometric studies in 10
patients revealed a significant decline in mean values on Global IQ scales.
Long-term survival with acceptable toxicity is possible following
aggressive, prompt treatment of meningeal relapse occurring after
prophylactic cranial irradiation. Hematologic relapse remains the major
obstacle to long-term disease-free survival.