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Article: Radiotherapy-induced glioblastoma: distinct differences in overall survival, tumor location, pMGMT methylation and primary tumor epidemiology in Hong Kong chinese patients
Title | Radiotherapy-induced glioblastoma: distinct differences in overall survival, tumor location, pMGMT methylation and primary tumor epidemiology in Hong Kong chinese patients |
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Authors | |
Keywords | Glioblastoma methyguanine methyltranferase radiation-induced radiotherapy-induced |
Issue Date | 2021 |
Citation | British Journal of Neurosurgery, 2021 How to Cite? |
Abstract | Introduction: Radiotherapy-induced glioblastomas (RIGB) are a well-known late and rare complication of brain irradiation. Yet the clinical, radiological and molecular characteristics of these tumors are not well characterized. Methods: This was a retrospective multicentre study that analysed adult patients with newly diagnosed glioblastoma over a 10-year period. Patients with RIGB were identified according to Cahan’s criteria for radiation-induced tumors. A case-control analysis was performed to compare known prognostic factors for overall survival (OS) with an independent cohort of IDH-1 wildtype de novo glioblastomas treated with standard temozolomide chemoradiotherapy. Survival analysis was performed by Cox proportional hazards regression. Results: A total of 590 adult patients were diagnosed with glioblastoma. 19 patients (3%) had RIGB. The mean age of patients upon diagnosis was 48 years ± 15. The mean latency duration from radiotherapy to RIGB was 14 years ± 8. The mean total dose was 58Gy ± 10. One-third of patients (37%, 7/19) had nasopharyngeal cancer and a fifth (21%, 4/19) had primary intracranial germinoma. Compared to a cohort of 146 de novo glioblastoma patients, RIGB patients had a shorter median OS of 4.8 months versus 19.2 months (p-value: <.001). Over a third of RIGBs involved the cerebellum (37%, 7/19) and was higher than the control group (4%, 6/146; p-value: <.001). A fifth of RIGBs (21%, 3/19) were pMGMT methylated which was significantly fewer than the control group (49%, 71/146; p-value:.01). For RIGB patients (32%, 6/19) treated with re-irradiation, the one-year survival rate was 67% and only 8% for those without such treatment (p-value:.007). Conclusion: The propensity for RIGBs to develop in the cerebellum and to be pMGMT unmethylated may contribute to their poorer prognosis. When possible re-irradiation may offer a survival benefit. Nasopharyngeal cancer and germinomas accounted for the majority of original malignancies reflecting their prevalence among Southern Chinese. |
Persistent Identifier | http://hdl.handle.net/10722/325516 |
ISSN | 2023 Impact Factor: 1.0 2023 SCImago Journal Rankings: 0.402 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Woo, Peter Y.M. | - |
dc.contributor.author | Lee, Jennifer W.Y. | - |
dc.contributor.author | Lam, Sandy W. | - |
dc.contributor.author | Pu, Jenny K.S. | - |
dc.contributor.author | Chan, Danny T.M. | - |
dc.contributor.author | Mak, Calvin H.K. | - |
dc.contributor.author | Ho, Jason M.K. | - |
dc.contributor.author | Wong, Sui To | - |
dc.contributor.author | Po, Yin Chung | - |
dc.contributor.author | Lee, Michael W.Y. | - |
dc.contributor.author | Chan, Kwong Yau | - |
dc.contributor.author | Poon, Wai Sang | - |
dc.date.accessioned | 2023-02-27T07:33:55Z | - |
dc.date.available | 2023-02-27T07:33:55Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | British Journal of Neurosurgery, 2021 | - |
dc.identifier.issn | 0268-8697 | - |
dc.identifier.uri | http://hdl.handle.net/10722/325516 | - |
dc.description.abstract | Introduction: Radiotherapy-induced glioblastomas (RIGB) are a well-known late and rare complication of brain irradiation. Yet the clinical, radiological and molecular characteristics of these tumors are not well characterized. Methods: This was a retrospective multicentre study that analysed adult patients with newly diagnosed glioblastoma over a 10-year period. Patients with RIGB were identified according to Cahan’s criteria for radiation-induced tumors. A case-control analysis was performed to compare known prognostic factors for overall survival (OS) with an independent cohort of IDH-1 wildtype de novo glioblastomas treated with standard temozolomide chemoradiotherapy. Survival analysis was performed by Cox proportional hazards regression. Results: A total of 590 adult patients were diagnosed with glioblastoma. 19 patients (3%) had RIGB. The mean age of patients upon diagnosis was 48 years ± 15. The mean latency duration from radiotherapy to RIGB was 14 years ± 8. The mean total dose was 58Gy ± 10. One-third of patients (37%, 7/19) had nasopharyngeal cancer and a fifth (21%, 4/19) had primary intracranial germinoma. Compared to a cohort of 146 de novo glioblastoma patients, RIGB patients had a shorter median OS of 4.8 months versus 19.2 months (p-value: <.001). Over a third of RIGBs involved the cerebellum (37%, 7/19) and was higher than the control group (4%, 6/146; p-value: <.001). A fifth of RIGBs (21%, 3/19) were pMGMT methylated which was significantly fewer than the control group (49%, 71/146; p-value:.01). For RIGB patients (32%, 6/19) treated with re-irradiation, the one-year survival rate was 67% and only 8% for those without such treatment (p-value:.007). Conclusion: The propensity for RIGBs to develop in the cerebellum and to be pMGMT unmethylated may contribute to their poorer prognosis. When possible re-irradiation may offer a survival benefit. Nasopharyngeal cancer and germinomas accounted for the majority of original malignancies reflecting their prevalence among Southern Chinese. | - |
dc.language | eng | - |
dc.relation.ispartof | British Journal of Neurosurgery | - |
dc.subject | Glioblastoma | - |
dc.subject | methyguanine methyltranferase | - |
dc.subject | radiation-induced | - |
dc.subject | radiotherapy-induced | - |
dc.title | Radiotherapy-induced glioblastoma: distinct differences in overall survival, tumor location, pMGMT methylation and primary tumor epidemiology in Hong Kong chinese patients | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1080/02688697.2021.1881445 | - |
dc.identifier.scopus | eid_2-s2.0-85100841822 | - |
dc.identifier.eissn | 1360-046X | - |
dc.identifier.isi | WOS:000617635400001 | - |