Limon Dror, Amiel Alexandra, Even Haim Shaked, Gordon Noa, Tschernichovsky Roi, Stemmer Salomon, Gal Omer, Laviv Yosef, Kanner Andrew, Siegal Tali, Yust-Katz Shlomit
Brain Tumor Center, Davidoff Cancer Center, Rabin Medical Center - Beilinson Hospital, Petach Tikva, Israel.
Radiation Oncology Unit, Davidoff Cancer Center, Rabin Medical Center - Beilinson Hospital, Petach Tikva, Israel.
Neurooncol Adv. 2024 Sep 16;6(1):vdae154. doi: 10.1093/noajnl/vdae154. eCollection 2024 Jan-Dec.
Atypical and anaplastic meningiomas account for 20% of all meningioma cases. Solitary fibrous tumor (SFT) is a type of soft tissue sarcoma with similar attributes to meningioma. For patients with refractory or recurrent disease after previous surgery or radiotherapy, there is no effective treatment. Pembrolizumab, an anti-programmed cell death 1 (PD-1) antibody, is an effective treatment for various solid tumors. PD-1 ligand is highly expressed in aggressive meningiomas. We aimed to assess the effectiveness of pembrolizumab in treating meningioma and SFT recurrence after surgery and radiation therapy.
This prospective single-arm phase II trial comprised 15 patients with recurrent meningioma and 3 with anaplastic SFT, treated at a single institution during 2018 to 2022. The study was terminated due to a lack of efficacy and slow accrual. The primary endpoint was 6-month progression-free survival (PFS-6).
Median progression-free survival (PFS) was 2.6 months, and median overall survival (OS) was 40 months. The 6- and 12-month PFS were both 11.1%. The 6- and 12-month OS were 94.4% and 61.1%, respectively. According to the Response Assessment in Neuro-Oncology (RANO) criteria, the overall response rate was 11%, with 2 patients achieving stable disease and 2 with partial response. Three patients (16.7%) developed grade 3 toxicity.
Our results showed that pembrolizumab failed to improve PFS-6 in patients with aggressive meningioma or anaplastic SFT. However, two patients, one with atypical meningioma and one with anaplastic SFT, achieved a partial response. More clinical studies are needed to identify which subset of patients may benefit from this treatment.
非典型和间变性脑膜瘤占所有脑膜瘤病例的20%。孤立性纤维瘤(SFT)是一种软组织肉瘤,具有与脑膜瘤相似的特征。对于既往手术或放疗后出现难治性或复发性疾病的患者,尚无有效的治疗方法。帕博利珠单抗是一种抗程序性细胞死亡1(PD-1)抗体,对各种实体瘤有效。PD-1配体在侵袭性脑膜瘤中高表达。我们旨在评估帕博利珠单抗治疗手术后和放疗后复发的脑膜瘤和SFT的有效性。
这项前瞻性单臂II期试验纳入了2018年至2022年期间在单一机构接受治疗的15例复发性脑膜瘤患者和3例间变性SFT患者。由于缺乏疗效和入组缓慢,该研究提前终止。主要终点是6个月无进展生存期(PFS-6)。
中位无进展生存期(PFS)为2.6个月,中位总生存期(OS)为40个月。6个月和12个月的PFS均为11.1%。6个月和12个月的OS分别为94.4%和61.1%。根据神经肿瘤学疗效评估(RANO)标准,总缓解率为11%,2例患者病情稳定,2例部分缓解。3例患者(16.7%)出现3级毒性反应。
我们的结果表明,帕博利珠单抗未能改善侵袭性脑膜瘤或间变性SFT患者的PFS-6。然而,1例非典型脑膜瘤患者和1例间变性SFT患者获得了部分缓解。需要更多的临床研究来确定哪些患者亚组可能从这种治疗中获益。