To describe dosimetry, acute toxicity, long-term survival and risk of second malignancies in children and adults treated with helical Tomotherapy craniospinal irradiation (HT-CSI). From 2006 to 2019, 58 pts (age 2-47 years, median 14) were treated with HT-CSI. The most common histologies were medulloblastoma (n = 40), CNS embryonal tumor NOS (formerly PNET) (n = 9) and intracranial GCT (n = 3). Other neoplasms were ATRT, ependymoma, glioma and ALL. 33 pts (57%) presented with distant dissemination or liquoral involvement. Among non-metastatic pts, a gross total resection was not achieved in 36% of cases. The prescribed HT-CSI doses were 23.4-36 Gy (1.6-1.8 Gy/fr) according to age-, tumor- and stage-specific protocols. Cases were contoured at one Pediatric Radiation Oncology Unit according to pediatric RT guidelines. Adjuvant, concurrent/adjuvant, neoadjuvant, neoadjuvant/adjuvant and no CT was administered in 31%, 17%, 17%, 23%, 12% of pts, respectively. A dosimetric analysis for PTVs and OARs was performed. Acute side effects were recorded according to the CTCAE 4.0. Survival analysis was performed by the Kaplan–Meier method. 3 cases of acute cerebral edema were reported in pts with massive intracranial disease and spinal involvement with implanted shunts. Considering only 39 pts not receiving CT or in complete recovery from mielotoxicity prior to HT-CSI, hematological toxicity included G1-4 leukopenia (5%, 18%, 41%, 15%, respectively), neutropenia (21%, 21%, 31% and 8%), thrombocytopenia (41%, 10%, 10% and 10%) and anemia (39%, 13%, 3% and 3%). No other G3–4 toxicity was reported. Apart from alopecia, the other most common G1-2 acute toxicities were nausea/vomiting (58% of pts), dermatitis (28%), anorexia/asthenia (14%), dysphagia (12%) and stomatitis (10%). The 3-, 5- and 10-year OS was 76%, 64% and 49%, respectively. Apart from 4 pts showing progression despite therapy, relapse after HT-CSI occurred in 18 pts. Rates of 3-, 5- and 10-year PFS from the end of RT were 59%, 56% and 41%, respectively. No second primary cancer occurred. Survival for pts with medulloblastoma included 3-, 5- and 10-year OS of 88%, 77% and 63%, respectively, and 3-, 5- and 10-year PFS of 77%, 67% and 60%, respectively. In the medulloblastoma group the 10-year OS/PFS resulted 53/54%, 67/75% and 91/59% for pts <=14, 14-25 and >25 years-old, respectively. M-status, surgical resection extension and CT regimen seemed to be associated to survival in an age-dependent manner. HT-CSI acute toxicity was in line with Literature. Further efforts to correlate dosimetric and toxicity data are needed. Long-term survival for pts with medulloblastoma resulted related to age. Older pts seemed to benefit from not receiving reduced-dose RT and different CT regimens. At a follow-up up to 11.5 years from the end of HT-CSI, no second malignancy occurred.
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