MBCL-10. LOCAL RECURRENCE AND SURVIVAL OUTCOMES OF MEDULLOBLASTOMA (MB) IN ADOLESCENT AND YOUNG ADULT PATIENTS (AYA). (4th December 2020)

• Record Type: Journal Article
• Authors: Rongthong, Warissara; Treechairusame, Teeradon; Suntornpong, Nan; Thephamongkhol, Kullathorn
• Is Part Of: Neuro-oncology. Volume 22(2020)Supplement 3
• Page Start: iii389
• Page End: iii389
• Publication Date: 2020-12-04
• Subjects: Brain Neoplasms -- Periodicals; Brain -- Tumors -- Periodicals; Brain -- Cancer -- Periodicals; Nervous system -- Cancer -- Periodicals; 616.99481
• DOI: 10.1093/neuonc/noaa222.486
• Languages: English
• ISSNs: 1522-8517

Abstract

Abstract: OBJECTIVE: The aim of this study is to evaluate the local recurrence-free survival (LRFS) and overall survival (OS) of MB in AYA patients at our institute. METHOD: Patients 15–39 years old with MB who was sent for post-operative radiation therapy (RT) in 2007 - 2017 at our institute were included. Kaplan-Meier statistics were used to estimate the LRFS and OS. RESULTS: Seven patients were included. The median age at RT was 18.3 years (16.7–28.6 years). Male was more common than female, 5 males vs. 2 females. NTR or GTR was achieved in 71.4% (5 in 7 patients). Only one patient had metastatic disease (M1) and received combined chemotherapy-RT. The rest 6 patients were received RT alone, all were M0. The median craniospinal irradiation (CSI) dose and total RT dose were 36Gy (23.4-46Gy) and 54Gy (54-56Gy), respectively. Five patients had available follow-up MRI brain. Local recurrence (LR) was found in one patient at 4.3 years after finished RT. Her initial treatment was subtotal resection (STR) followed by RT alone; CSI 36 Gy and posterior fossa boost to 55.8Gy. The 2-years and 5-years LRFS were 100% and 66.7%, respectively. Both 2-years and 5-years OS were 100%. The median follow-up time was 7.6 years (0.4–11.5 years). CONCLUSION: Our study shows high 2-years LRFS and OS of post-operative RT alone in AYA MB. Combined chemotherapy-RT should be considered in STR or M1. More number of patients and molecular histopathology subtype reports are still needed to confirm this report.