Cited 0 times in
Choosing Wisely between Radiotherapy Dose-Fractionation Schedules: The Molecular Graded Prognostic Assessment for Elderly Glioblastoma Patients
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 위찬우 | - |
dc.contributor.author | 윤홍인 | - |
dc.contributor.author | 조재호 | - |
dc.contributor.author | 김진아 | - |
dc.date.accessioned | 2025-05-02T00:29:45Z | - |
dc.date.available | 2025-05-02T00:29:45Z | - |
dc.date.issued | 2025-04 | - |
dc.identifier.issn | 1598-2998 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/205404 | - |
dc.description.abstract | Purpose: This study aimed to develop a graded prognostic assessment (GPA) model integrating genomic characteristics for elderly patients with glioblastoma (eGBM), and to compare the efficacy of different radiotherapy schedules. Materials and methods: This multi-institutional retrospective study included patients aged ≥ 65 years who underwent surgical resection followed by radiotherapy with or without temozolomide (TMZ) for newly diagnosed eGBM. Based on the significant factors identified in the multivariate analysis for overall survival (OS), the molecular GPA for eGBM (eGBM-molGPA) was established. Results: A total of 334 and 239 patients who underwent conventionally fractionated radiotherapy (CFRT) and hypofractionated radiotherapy (HFRT) were included, respectively, with 86% of patients receiving TMZ-based chemoradiation. With a median follow-up of 17.4 months (range, 3.3 to 149.9 months), the median OS was 18.7 months for CFRT+TMZ group, 15.1 months for HFRT+TMZ group, and 10.4 months for radiotherapy alone group (CFRT+TMZ vs. HFRT+TMZ: hazard ratio [HR], 1.52; p < 0.001 and CFRT+TMZ vs. radiotherapy alone: HR, 2.52; p < 0.001). In a combined analysis with the NOA-08 and Nordic trials, CFRT+TMZ group exhibited the highest survival rates among all treatment groups. The eGBM-molGPA, which integrated four clinical and three molecular parameters, stratified patients into low-, intermediate-, and high-risk groups. CFRT+TMZ significantly improved OS compared to HFRT+TMZ or radiotherapy alone in the low-risk (p=0.023) and intermediate-risk groups (p < 0.001). However, in the high-risk group, there was no significant difference in OS between treatment options (p=0.770). Conclusion: CFRT+TMZ may be more effective than HFRT+TMZ or radiotherapy alone for selected eGBM patients. The novel eGBM-molGPA model can guide treatment selection for this patient population. | - |
dc.description.statementOfResponsibility | open | - |
dc.format | application/pdf | - |
dc.language | English, Korean | - |
dc.publisher | Official journal of Korean Cancer Association | - |
dc.relation.isPartOf | CANCER RESEARCH AND TREATMENT | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Brain Neoplasms* / genetics | - |
dc.subject.MESH | Brain Neoplasms* / mortality | - |
dc.subject.MESH | Brain Neoplasms* / pathology | - |
dc.subject.MESH | Brain Neoplasms* / radiotherapy | - |
dc.subject.MESH | Brain Neoplasms* / therapy | - |
dc.subject.MESH | Chemoradiotherapy / methods | - |
dc.subject.MESH | Dose Fractionation, Radiation* | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Glioblastoma* / genetics | - |
dc.subject.MESH | Glioblastoma* / mortality | - |
dc.subject.MESH | Glioblastoma* / pathology | - |
dc.subject.MESH | Glioblastoma* / radiotherapy | - |
dc.subject.MESH | Glioblastoma* / therapy | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Temozolomide / therapeutic use | - |
dc.subject.MESH | Treatment Outcome | - |
dc.title | Choosing Wisely between Radiotherapy Dose-Fractionation Schedules: The Molecular Graded Prognostic Assessment for Elderly Glioblastoma Patients | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Radiation Oncology (방사선종양학교실) | - |
dc.contributor.googleauthor | Hye In Lee | - |
dc.contributor.googleauthor | Jina Kim | - |
dc.contributor.googleauthor | In Ah Kim | - |
dc.contributor.googleauthor | Joo Ho Lee | - |
dc.contributor.googleauthor | Jaeho Cho | - |
dc.contributor.googleauthor | Rifaquat Rahman | - |
dc.contributor.googleauthor | Geoffrey Fell | - |
dc.contributor.googleauthor | Chan Woo Wee | - |
dc.contributor.googleauthor | Hong In Yoon | - |
dc.identifier.doi | 10.4143/crt.2024.680 | - |
dc.contributor.localId | A06487 | - |
dc.contributor.localId | A04777 | - |
dc.contributor.localId | A03901 | - |
dc.relation.journalcode | J00453 | - |
dc.identifier.eissn | 2005-9256 | - |
dc.identifier.pmid | 39265619 | - |
dc.subject.keyword | Aged | - |
dc.subject.keyword | Glioblastoma | - |
dc.subject.keyword | Graded prognostic assessment | - |
dc.subject.keyword | Molecular biomarker | - |
dc.subject.keyword | Radiotherapy | - |
dc.subject.keyword | Temozolomide | - |
dc.contributor.alternativeName | Wee, Chan Woo | - |
dc.contributor.affiliatedAuthor | 위찬우 | - |
dc.contributor.affiliatedAuthor | 윤홍인 | - |
dc.contributor.affiliatedAuthor | 조재호 | - |
dc.citation.volume | 57 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 378 | - |
dc.citation.endPage | 386 | - |
dc.identifier.bibliographicCitation | CANCER RESEARCH AND TREATMENT, Vol.57(2) : 378-386, 2025-04 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.