Alker Jan Paul, Rahmanzade Ramin, Held Thomas, Herold-Mende Christel, Unterberg Andreas, Sahm Felix, Krieg Sandro Manuel, Jungwirth Gerhard
Department of Neurosurgery, Heidelberg University, Heidelberg, Germany.
Department of Neuropathology, Heidelberg University, Heidelberg, Germany.
Neurooncol Adv. 2025 Apr 17;7(1):vdaf077. doi: 10.1093/noajnl/vdaf077. eCollection 2025 Jan-Dec.
Solitary fibrous tumors (SFTs)/hemangiopericytoma are rare central nervous system tumors exhibiting high recurrence rates and the ability to metastasize. This study evaluated SFT prognosis and survival outcomes, focusing on the 2021 WHO classification.
A retrospective study was conducted on 49 patients who underwent SFT resection in our Neurosurgery Department between 2001 and 2023. Data were analyzed regarding sex, age, WHO grade at time of diagnosis and reclassified according to the 2021 WHO classification, tumor localization, resection grade, tumor size, adjuvant therapy, progression-free (PFS), and overall survival (OS). Kaplan-Meier survival analyses were conducted to evaluate OS and PFS, and Cox regression analyses were performed to assess prognostic factors.
Cohort median age was 54 (22-86) years with a female predominance of 1.22. The median follow-up was 46 (0-307) months. Primary SFTs were mainly located in the supratentorial region, followed by the infratentorial region and spine. Initially, 10% of primary tumors were graded as WHO grade 1, 49% as grade 2, and 18% as grade 3. Reclassification to WHO 2021 downgraded 65% of tumors. The five-year PFS and OS were 41.5% and 100%, respectively. In total, 41% of patients had local recurrent disease and 20% were metastatic. In univariate analyses, WHO grades, younger age (< 54 years), sex, and adjuvant radiotherapy were associated with survival. In multivariate analyses, WHO grade 3, metastatic disease, and adjuvant radiotherapy were independent PFS prognostic factors.
Our data shows that WHO grade 3, metastatic disease, and adjuvant radiotherapy are independent PFS factors in SFTs.
孤立性纤维瘤(SFTs)/血管外皮细胞瘤是罕见的中枢神经系统肿瘤,具有高复发率和转移能力。本研究评估了SFT的预后和生存结局,重点关注2021年世界卫生组织(WHO)分类。
对2001年至2023年间在我院神经外科接受SFT切除术的49例患者进行回顾性研究。分析患者的性别、年龄、诊断时的WHO分级,并根据2021年WHO分类重新分类,肿瘤定位、切除分级、肿瘤大小、辅助治疗、无进展生存期(PFS)和总生存期(OS)。采用Kaplan-Meier生存分析评估OS和PFS,并进行Cox回归分析以评估预后因素。
队列中位年龄为54(22 - 86)岁,女性占优势,男女比例为1.22。中位随访时间为46(0 - 307)个月。原发性SFT主要位于幕上区域,其次是幕下区域和脊柱。最初,10%的原发性肿瘤为WHO 1级,49%为2级,18%为3级。重新分类为2021年WHO分级后,65%的肿瘤级别降低。五年PFS和OS分别为41.5%和100%。共有41%的患者出现局部复发,20%发生转移。单因素分析中,WHO分级、年龄较小(<54岁)、性别和辅助放疗与生存相关。多因素分析中,WHO 3级、转移疾病和辅助放疗是独立的PFS预后因素。
我们的数据表明,WHO 3级、转移疾病和辅助放疗是SFTs独立的PFS因素。