Proton-Based Radiation Therapy for Skull Base Chondrosarcomas in Children and Adolescents: 40-Year Experience From the Massachusetts General Hospital.

IF 6.4 1区 医学 Q1 ONCOLOGY
Myrsini Ioakeim-Ioannidou, Saveli Goldberg, Tobias Urell, Athena Tejada, G Petur Nielsen, Yin P Hung, Judith Adams, Barbara Fullerton, Paul Caruso, Manuel Patino, Karen Buch, Sandra Rincon, Osamu Sakai, Maria Tolia, David Ebb, Gregory Cote, William Curry, Drosoula Giantsoudi, Shannon M MacDonald
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引用次数: 0

Abstract

Purpose: The literature on skull base chondrosarcoma (CHS) is scarce. We report outcomes for pediatric and young patients ≤22 years with base of skull CHSs treated with proton-based radiation therapy (PBRT).

Methods and materials: We retrospectively reviewed all patients treated with PBRT between 1981 and 2023. Primary endpoints were overall survival (OS), chondrosarcoma-specific survival (CSS), progression-free survival (PFS), local control, and distal control.

Results: Eighty-four patients were identified. Median age at diagnosis was 19 years (range, 6-22). Most patients (n = 79, 94%) had conventional CHS, whereas 5 (6%) had mesenchymal CHS. Nine patients (11%) underwent gross total resection, 64 (76%) subtotal resection, and 11 patients (13%) underwent biopsy. Twenty-four (29%) patients progressed before radiation therapy. The median prescription dose was 70 Gy (relative biological equivalent) (range, 50-79.7). At a median follow-up of 18.0 years (IQR, 9.2-26.2) from diagnosis, 11 patients recurred (7 local, 4 distant). Six patients died of disease. Five patients died of other causes. Ten-year OS, CSS, and PFS rates for all patients were 93.3%, 94.7%, and 88%, respectively. Twenty-year OS, CSS, and PFS rates for conventional CHS (n = 79) were 93.1%, 97.1%, and 89.2%, respectively. Mesenchymal histology was significantly associated with worse OS and PFS. Preradiation therapy tumor progression portended worse OS and CSS. Eight patients (9.9 %) experienced a late toxicity grade 3 or greater.

Conclusions: This is the largest cohort of pediatric base of skull CHSs in literature to date. High-dose PBRT after surgical resection achieves excellent disease control with minimal toxicity.

儿童和青少年颅底软骨肉瘤的质子放射治疗:来自一家医疗机构的 40 年经验
背景:有关颅底软骨肉瘤(CHS)的文献很少。我们报告了颅底(BOS)软骨肉瘤患者中年龄小于22岁的儿童和年轻患者接受质子放疗(PBRT)治疗的结果:我们对 1981 年至 2023 年间接受质子放疗的所有患者进行了回顾性研究。主要终点为总生存期(OS)、软骨肉瘤特异性生存期(CSS)、无进展生存期(PFS)、局部控制(LC)和远端控制(DC):结果:共发现 84 例患者。确诊时的中位年龄为19岁(6-22岁)。大多数患者(79人,94%)为传统CHS,5人(6%)为间充质CHS。9名患者(11%)接受了全切除术(GTR),64名患者(76%)接受了次全切除术(STR),11名患者(13%)接受了活组织检查。24例(29%)患者在接受放疗(RT)前病情有所进展。处方剂量中位数为 70 Gy(RBE)(范围为 50 - 79.7)。在确诊后中位随访18.0年[四分位距(IQR),9.2 -26.2]期间,11名患者复发(7名局部复发,4名远处复发)。6 名患者死于疾病。五名患者死于其他原因。所有患者的十年 OS、CSS 和 PFS 分别为 93.3%、94.7% 和 88%。传统CHS(79人)的20年OS、CSS和PFS率分别为93.1%、97.1%和89.2%。间质组织学与较差的 OS 和 PFS 显著相关。RT前肿瘤进展预示着更差的OS和CSS。8名患者(9.9%)的晚期毒性达到或超过3级:这是迄今为止文献中规模最大的小儿BOS CHS队列。结论:这是迄今为止文献报道中规模最大的一组小儿 BOS CHS。手术切除后进行大剂量 PBRT 治疗,可实现良好的疾病控制,且毒性极低。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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