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Efficacy of Whole-Ventricular Radiotherapy in Patients Undergoing Maximal Tumor Resection for Glioblastomas Involving the Ventricle
DC Field | Value | Language |
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dc.contributor.author | 강석구 | - |
dc.contributor.author | 김경환 | - |
dc.contributor.author | 문주형 | - |
dc.contributor.author | 변화경 | - |
dc.contributor.author | 서창옥 | - |
dc.contributor.author | 유지환 | - |
dc.contributor.author | 윤홍인 | - |
dc.contributor.author | 장종희 | - |
dc.date.accessioned | 2021-12-28T16:44:58Z | - |
dc.date.available | 2021-12-28T16:44:58Z | - |
dc.date.issued | 2021-09 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/186783 | - |
dc.description.abstract | Background and purpose: Patients with glioblastoma (GBM) involving the ventricles are at high risk of ventricle opening during surgery and potential ventricular tumor spread. We evaluated the effectiveness of whole-ventricular radiotherapy (WVRT) in reducing intraventricular seeding in patients with GBM and identified patients who could benefit from this approach. Methods and materials: We retrospectively reviewed the data of 382 patients with GBM who underwent surgical resection and temozolomide-based chemoradiotherapy. Propensity score matching was performed to compensate for imbalances in characteristics between patients who did [WVRT (+); n=59] and did not [WVRT (-); n=323] receive WVRT. Local, outfield, intraventricular, and leptomeningeal failure rates were compared. Results: All patients in the WVRT (+) group had tumor ventricular involvement and ventricle opening during surgery. In the matched cohort, the WVRT (+) group exhibited a significantly lower 2-year intraventricular failure rate than the WVRT (-) group (2.1% vs. 11.8%; P=0.045), with no difference in other outcomes. Recursive partitioning analysis stratified the patients in the WVRT (-) group at higher intraventricular failure risk (2-year survival, 14.2%) due to tumor ventricular involvement, MGMT unmethylation, and ventricle opening. WVRT reduced the intraventricular failure rate only in high-risk patients (0% vs. 14.2%; P=0.054) or those with MGMT-unmethylated GBM in the matched cohort (0% vs. 17.3%; P=0.036). Conclusions: WVRT reduced the intraventricular failure rate in patients with tumor ventricular involvement and ventricle opening during surgery. The MGMT-methylation status may further stratify patients who could benefit from WVRT. Further prospective evaluation of WVRT in GBM is warranted. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | Frontiers Research Foundation | - |
dc.relation.isPartOf | FRONTIERS IN ONCOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | Efficacy of Whole-Ventricular Radiotherapy in Patients Undergoing Maximal Tumor Resection for Glioblastomas Involving the Ventricle | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Neurosurgery (신경외과학교실) | - |
dc.contributor.googleauthor | Kyung Hwan Kim | - |
dc.contributor.googleauthor | Jihwan Yoo | - |
dc.contributor.googleauthor | Nalee Kim | - |
dc.contributor.googleauthor | Ju Hyung Moon | - |
dc.contributor.googleauthor | Hwa Kyung Byun | - |
dc.contributor.googleauthor | Seok-Gu Kang | - |
dc.contributor.googleauthor | Jong Hee Chang | - |
dc.contributor.googleauthor | Hong In Yoon | - |
dc.contributor.googleauthor | Chang-Ok Suh | - |
dc.identifier.doi | 10.3389/fonc.2021.736482 | - |
dc.contributor.localId | A00036 | - |
dc.contributor.localId | A05226 | - |
dc.contributor.localId | A01383 | - |
dc.contributor.localId | A05136 | - |
dc.contributor.localId | A01919 | - |
dc.contributor.localId | A05158 | - |
dc.contributor.localId | A04777 | - |
dc.contributor.localId | A03470 | - |
dc.relation.journalcode | J03512 | - |
dc.identifier.eissn | 2234-943X | - |
dc.identifier.pmid | 34621677 | - |
dc.subject.keyword | MGMT | - |
dc.subject.keyword | glioblastoma | - |
dc.subject.keyword | radiotherapy | - |
dc.subject.keyword | temozolomide | - |
dc.subject.keyword | ventricle | - |
dc.contributor.alternativeName | Kang, Seok Gu | - |
dc.contributor.affiliatedAuthor | 강석구 | - |
dc.contributor.affiliatedAuthor | 김경환 | - |
dc.contributor.affiliatedAuthor | 문주형 | - |
dc.contributor.affiliatedAuthor | 변화경 | - |
dc.contributor.affiliatedAuthor | 서창옥 | - |
dc.contributor.affiliatedAuthor | 유지환 | - |
dc.contributor.affiliatedAuthor | 윤홍인 | - |
dc.contributor.affiliatedAuthor | 장종희 | - |
dc.citation.volume | 11 | - |
dc.citation.startPage | 736482 | - |
dc.identifier.bibliographicCitation | FRONTIERS IN ONCOLOGY, Vol.11 : 736482, 2021-09 | - |
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