was seen in 13 and recurrence in 7 patients (3 had prior RT to brain or spine). All had chemotherapy, and 42% received HD-AuSCR prior to CSI. All but two required anesthesia. In total, 270 fractions were delivered. Duration of CSI was a median of 20 days (max 30) with a median daily setup and radiation time of 20 minutes. The longest treatment times for each patient varied due to setup difficulties or anesthetic issues (25% >1 hour, max 76 min). The median CSI PTV was 2294cm 3 , with excellent PTV coverage (V95 mean 98.9%, V107 mean 7.4%, point dose <112%). As a percentage of CSI dose, the mean doses to the lenses, thyroid, and heart were 34.8%, 35.5%, and 30.6%, respectively. The mean lung V5 was 65% and V20 was 2.8%. With a short median follow-up of 7 months, 5 patients progressed (2 local, 3 leptomeningeal) at a median of 3.5 months post CSI; 2 died of disease. The most common acute toxicity was hematologic: lymphopenia (11% Grade 2, 26% Gr 3, 63% Gr 4), anemia (89% Gr 2), and thrombocytopenia (16% Gr 1-2, 26% Gr 3, 37% Gr 4). Despite lymphopenia, we encountered only two Gr 3 infections (UTI and lung). The majority required blood products (89% RBC, 68% platelets). Weight loss was also common (47% Gr 1, 26% Gr 2). Conclusion: Volume modulated arc therapy CSI, along with chemotherapy and anesthesia, is feasible with supportive care. Daily IGRT without matched-and-feathered field junctions improves accuracy and reduces the risk of spinal cord overdose without increasing treatment time. Further research is needed to determine whether reducing doses to organs, such as thyroid, heart, or hippocampus offsets the risk of increased volume of lowdose irradiation.