Proton beam therapy in a patient with secondary glioblastoma (32 years after postoperative irradiation of medulloblastoma): case report and literature review

被引:1
作者
Bai, Jiwei [1 ]
Abulimiti, Muyasha [2 ]
Jin, Yonglong [3 ,4 ]
Wang, Jie [5 ]
Zhang, Shuyan [6 ]
Liu, Chao [6 ]
Wang, Zishen [5 ]
Wang, Wei [7 ]
Li, Yinuo [8 ]
Wang, Weiwei [6 ]
Yang, Lu [6 ]
Shimizu, Shosei [6 ,8 ]
机构
[1] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurosurg, Beijing 100050, Peoples R China
[2] Univ Tsukuba, Grad Sch Comprehens Human Sci, Dept Radiat Oncol, Tsukuba 3058575, Japan
[3] Qingdao Univ, Affiliated Hosp, Dept Radiotherapy, Qingdao, Peoples R China
[4] Qingdao Univ, Sch Publ Hlth, Qingdao 266071, Peoples R China
[5] Hebei Yizhou Canc Hosp, Dept Radiotherapy Phys & Technol, Zhuozhou 072750, Peoples R China
[6] Hebei Yizhou Canc Hosp, Radiat Therapy Ctr, Pediat Proton Beam Therapy Ctr, Dept Pediat, Zhuozhou 072750, Peoples R China
[7] Hebei Yizhou Canc Hosp, Dept Radiol, Zhuozhou 072750, Peoples R China
[8] Univ Tsukuba Hosp, Dept Pediat, Tsukuba 3058576, Japan
关键词
Medulloblastoma; Second primary tumor; Radiation-induced glioblastoma; Proton beam radiotherapy; CHILDHOOD-CANCER; MUTATIONS; NEOPLASMS; SURVIVORS; TUMORS; RISK; 5TH;
D O I
10.1186/s13014-024-02515-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ObjectiveThis report details the experience of a patient who developed a second primary glioblastoma (GB), offering insights into the treatment process and reviewing relevant literature.Case presentationA male patient, who was diagnosed with medulloblastoma at age 9, received treatment with cobalt-60 craniospinal irradiation (CSI) (36 Gy/20 fractions) and a tumor bed boost (total of 56 Gy). After 32 years, at age 41, an MRI revealed a space-occupying mass in the left cerebellar hemisphere. Surgical resection was performed, and postoperative pathology confirmed a diagnosis of radiation-induced glioblastoma (RIGB). Given the history of irradiation and the current tolerability of brainstem doses, proton beam therapy (PBT) combined with Temozolomide (75 mg/m2) was chosen. The treatment plan included 60 Gy on the gross tumor bed and 54 Gy on the clinical target volume, delivered in 30 fractions. The patient underwent regular follow-up and achieved a complete response.Clinical discussionFor childhood cancer survivors, the development of a second primary tumor significantly impacts prognosis. RIGB is a rare form of secondary tumor with distinct molecular characteristics compared to primary GB and recurrent secondary GB. Molecular markers such as IDH and MGMT status can help differentiate between primary GB, recurrent secondary GB, and radiation-induced secondary GB in patients with a history of prior radiation therapy. Surgical resection remains a primary treatment option, while PBT is preferred for postoperative treatment due to its superior protection of normal tissues and the ability to deliver high-dose irradiation.ConclusionRIGB is a rare second primary tumor that requires strategic molecular profiling and individualized management. Proton beam therapy provides effective high-dose irradiation in the postoperative phase and is the preferred treatment option for such cases.
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页数:8
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