Cacciotti Chantel, Liu Kevin X, Haas-Kogan Daphne A, Warren Katherine E
Dana Farber/Boston Children's Cancer and Blood Disorder Center, Boston, Massachusetts.
Department of Radiation-Oncology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Boston, Massachusetts.
Neurooncol Pract. 2020 Oct 6;8(1):68-74. doi: 10.1093/nop/npaa063. eCollection 2021 Feb.
Diffuse intrinsic pontine gliomas (DIPGs) are a leading cause of brain tumor deaths in children. Current standard of care includes focal radiation therapy (RT). Despite clinical improvement in most patients, the effect is temporary and median survival is less than 1 year. The use and benefit of reirradiation have been reported in progressive DIPG, yet standardized approaches are lacking. We conducted a survey to assess reirradiation practices for DIPG in North America.
A 14-question REDCap survey was disseminated to 396 North American physicians who care for children with CNS tumors.
The response rate was 35%. Participants included radiation-oncologists (63%; 85/135) and pediatric oncologists/neuro-oncologists (37%; 50/135). Most physicians (62%) treated 1 to 5 DIPG patients per year, with 10% treating more than 10 patients per year. Reirradiation was considered a treatment option by 88% of respondents. Progressive disease and worsening clinical status were the most common reasons to consider reirradiation. The majority (84%) surveyed considered reirradiation a minimum of 6 months following initial RT. Doses varied, with median total dose of 2400 cGy (range, 1200-6000 cGy) and fraction size of 200 cGy (range, 100-900 cGy). Concurrent use of systemic agents with reirradiation was considered in 46%, including targeted agents (37%), biologics (36%), or immunotherapy (25%). One-time reirradiation was the most common practice (71%).
Although the vast majority of physicians consider reirradiation as a treatment for DIPG, total doses and fractionation varied. Further clinical trials are needed to determine the optimal radiation dose and fractionation for reirradiation in children with progressive DIPG.
弥漫性脑桥内在型胶质瘤(DIPG)是儿童脑肿瘤死亡的主要原因。当前的标准治疗包括局部放射治疗(RT)。尽管大多数患者临床症状有所改善,但效果是暂时的,中位生存期不足1年。复发性放射治疗在进展性DIPG中的应用及益处已有报道,但缺乏标准化方法。我们开展了一项调查,以评估北美地区DIPG的复发性放射治疗实践。
向396名诊治中枢神经系统肿瘤患儿的北美医生发放了一份包含14个问题的REDCap调查问卷。
回复率为35%。参与者包括放射肿瘤学家(63%;85/135)和儿科肿瘤学家/神经肿瘤学家(37%;50/135)。大多数医生(62%)每年治疗1至5例DIPG患者,10%的医生每年治疗超过10例患者。88%的受访者认为复发性放射治疗是一种治疗选择。疾病进展和临床状况恶化是考虑复发性放射治疗最常见的原因。大多数(84%)受访者认为在初次放疗后至少6个月进行复发性放射治疗。剂量各不相同,总剂量中位数为2400 cGy(范围为1200 - 6000 cGy),分次剂量为200 cGy(范围为100 - 900 cGy)。46%的受访者考虑在复发性放射治疗时同时使用全身药物,包括靶向药物(37%)、生物制剂(36%)或免疫疗法(25%)。单次复发性放射治疗是最常见的做法(71%)。
尽管绝大多数医生认为复发性放射治疗可用于DIPG的治疗,但总剂量和分割方式各不相同。需要进一步开展临床试验,以确定进展性DIPG患儿复发性放射治疗的最佳放射剂量和分割方式。