Department of Radiation Oncology, Miulli General Regional Hospital, Acquaviva delle Fonti-Bari, Italy.
Department of Medical Oncology, Miulli General Regional Hospital, Acquaviva delle Fonti-Bari, Italy.
Strahlenther Onkol. 2024 Sep;200(9):751-759. doi: 10.1007/s00066-023-02172-9. Epub 2023 Nov 21.
No standard treatment has yet been established for recurrent glioblastoma (GBM). In this context, the aim of the current study was to evaluate safety and efficacy of reirradiation (re-RT) by radiosurgery or fractionated stereotactic radiotherapy (SRS/FSRT) in association with regorafenib.
Patients with a histological or radiological diagnosis of recurrent GBM who received re-RT by SRS/FSRT and regorafenib as second-line systemic therapy were included in the analysis.
From January 2020 to December 2022, 21 patients were evaluated. The median time between primary/adjuvant RT and disease recurrence was 8 months (range 5-20). Median re-RT dose was 24 Gy (range 18-36 Gy) for a median number of 5 fractions (range 1-6). Median regorafenib treatment duration was 12 weeks (range 3-26). Re-RT was administered before starting regorafenib or in the week off regorafenib during the course of chemotherapy. The median and the 6‑month overall survival (OS) from recurrence were 8.4 months (95% confidence interval [CI] 6.9-12.7 months) and 75% (95% CI 50.9-89.1%), respectively. The median progression-free survival (PFS) from recurrence was 6 months (95% CI 3.7-8.5 months). The most frequent side effects were asthenia that occurred in 10 patients (8 cases of grade 2 and 2 cases of grade 3), and hand-foot skin reaction (2 patients grade 3, 3 patients grade 2). Adverse events led to permanent regorafenib discontinuation in 2 cases, while in 5/21 cases (23.8%), a dose reduction was administered. One patient experienced dehiscence of the surgical wound after reintervention and during regorafenib treatment, while another patient reported intestinal perforation that required hospitalization.
For recurrent GBM, re-RT with SRT/FSRT plus regorafenib is a safe treatment. Prospective trials are necessary.
目前尚无标准疗法可用于复发性胶质母细胞瘤(GBM)的治疗。因此,本研究旨在评估在接受立体定向放射外科(SRS/FSRT)或分割立体定向放疗(SRS/FSRT)再放疗(re-RT)联合瑞戈非尼治疗的复发性 GBM 患者中的安全性和有效性。
回顾性分析 2020 年 1 月至 2022 年 12 月期间,在我院接受 SRS/FSRT 联合瑞戈非尼二线全身治疗的复发性 GBM 患者的临床资料。
共纳入 21 例患者,中位复发至 re-RT 时间为 8 个月(5-20 个月),中位再放疗剂量为 24 Gy(18-36 Gy),分割次数为 5 次(1-6 次)。中位瑞戈非尼治疗时间为 12 周(3-26 周)。re-RT 在开始瑞戈非尼治疗前或化疗期间的瑞戈非尼停药周内进行。从复发开始的中位总生存期(OS)和 6 个月 OS 率分别为 8.4 个月(95%CI 6.9-12.7 个月)和 75%(95%CI 50.9-89.1%)。从复发开始的中位无进展生存期(PFS)为 6 个月(95%CI 3.7-8.5 个月)。最常见的不良反应为乏力,共 10 例患者(8 例 2 级,2 例 3 级),手足皮肤反应 2 例(3 级,3 例 2 级)。有 2 例患者因不良反应而永久停止使用瑞戈非尼,5 例(23.8%)患者减少了剂量。1 例患者在 re-RT 治疗和瑞戈非尼治疗期间发生手术切口裂开,另 1 例患者发生肠道穿孔需要住院治疗。
对于复发性 GBM,SRS/FSRT 联合瑞戈非尼再放疗是一种安全的治疗方法。需要进行前瞻性研究。