PMID- 26675376 OWN - NLM STAT- MEDLINE DCOM- 20161221 LR - 20181113 IS - 1949-2553 (Electronic) IS - 1949-2553 (Linking) VI - 7 IP - 7 DP - 2016 Feb 16 TI - Analysis of risk and predictors of brain radiation necrosis after radiosurgery. PG - 7773-9 LID - 10.18632/oncotarget.6532 [doi] AB - In this study, we examined the factors contributing to brain radiation necrosis and its predictors of patients treated with Cyberknife radiosurgery. A total of 94 patients with primary or metastatic brain tumours having been treated with Cyberknife radiotherapy from Sep. 2006 to Oct. 2011 were collected and retrospectively analyzed. Skull based tracking was used to deliver radiation to 104 target sites. and the prescribed radiation doses ranged from 1200 to 4500 cGy in 1 to 8 fractions with a 60% to 87% isodose line. Radiation necrosis was confirmed by imaging or pathological examination. Associations between cerebral radiation necrosis and factors including diabetes, cardio-cerebrovascular disease, target volume, isodose line, prescribed dosage, number of fractions, combination with whole brain radiation and biologically equivalent dose (BED) were determined by logistic regression. ROC curves were created to measure the predictive accuracy of influence factors and identify the threshold for brain radiation necrosis. Our results showed that radiation necrosis occurred in 12 targets (11.54%). Brain radiation necrosis was associated by BED, combination with whole brain radiotherapy, and fractions (areas under the ROC curves = 0.892+/-0.0335, 0.650+/-0.0717, and 0.712+/-0.0637 respectively). Among these factors, only BED had the capability to predict brain radiation necrosis, and the threshold dose was 7410 cGy. In conclusion, BED is the most effective predictor of brain radiation necrosis, with a dose of 7410 cGy being identified as the threshold. FAU - Zhuang, Hongqing AU - Zhuang H AD - Department of Radiotherapy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy and Tianjin Lung Cancer Center, Tianjin, China. FAU - Zheng, Yi AU - Zheng Y AD - Daqing Oilfield General Hospital, Heilongjiang, China. FAU - Wang, Junjie AU - Wang J AD - Department of Radiotherapy, Peking University 3rd Hospital, Beijing, China. FAU - Chang, Joe Y AU - Chang JY AD - Department of Radiation Oncology, Division of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. FAU - Wang, Xiaoguang AU - Wang X AD - Department of Radiotherapy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy and Tianjin Lung Cancer Center, Tianjin, China. FAU - Yuan, Zhiyong AU - Yuan Z AD - Department of Radiotherapy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy and Tianjin Lung Cancer Center, Tianjin, China. FAU - Wang, Ping AU - Wang P AD - Department of Radiotherapy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy and Tianjin Lung Cancer Center, Tianjin, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Oncotarget JT - Oncotarget JID - 101532965 SB - IM MH - Adolescent MH - Adult MH - Aged MH - Aged, 80 and over MH - Brain Neoplasms/*secondary/surgery MH - Child MH - Female MH - Follow-Up Studies MH - Humans MH - Male MH - Middle Aged MH - Necrosis MH - Neoplasm Staging MH - Neoplasms/*pathology/surgery MH - Prognosis MH - Radiation Injuries/etiology/*pathology MH - Radiosurgery/*adverse effects MH - Radiotherapy Dosage MH - Retrospective Studies MH - Risk Factors MH - Young Adult PMC - PMC4884953 OTO - NOTNLM OT - Cyberknife OT - biologically equivalent dose (BED) OT - brain radiation necrosis OT - stereotactic radiotherapy (SRT) COIS- CONFLICTS OF INTEREST The authors declare no conflicts of interest. EDAT- 2015/12/18 06:00 MHDA- 2016/12/22 06:00 PMCR- 2016/02/16 CRDT- 2015/12/18 06:00 PHST- 2015/08/19 00:00 [received] PHST- 2015/11/25 00:00 [accepted] PHST- 2015/12/18 06:00 [entrez] PHST- 2015/12/18 06:00 [pubmed] PHST- 2016/12/22 06:00 [medline] PHST- 2016/02/16 00:00 [pmc-release] AID - 6532 [pii] AID - 10.18632/oncotarget.6532 [doi] PST - ppublish SO - Oncotarget. 2016 Feb 16;7(7):7773-9. doi: 10.18632/oncotarget.6532.