Yoo Stella K, Strickland Ben A, Zada Gabriel, Bian Shelly X, Garsa Adam, Ye Jason C, Yu Cheng, Weiss Martin H, Wrobel Bozena B, Giannotta Steven, Chang Eric L
Department of Radiation Oncology, University of Southern California, Keck School of Medicine, Los Angeles, California, United States.
Department of Neurosurgery, University of Southern California, Keck School of Medicine, Los Angeles, California, United States.
J Neurol Surg B Skull Base. 2021 Apr;82(2):161-174. doi: 10.1055/s-0039-3402019. Epub 2020 Jan 14.
Chordomas are locally destructive neoplasms characterized by appreciable recurrence rates after initial multimodality treatment. We examined the outcome of salvage treatment in recurrent/progressive skull base chordomas. This is a retrospective review of recurrent/progressive skull base chordomas at a tertiary urban academic medical center. The outcomes evaluated were overall survival, progression-free survival (PFS), and incidence of new toxicity. Eighteen consecutive patients who underwent ≥1 course of treatment (35.3% salvage surgery, 23.5% salvage radiation, and 41.2% both) were included. The median follow-up was 98.6 months (range 16-215 months). After initial treatment, the median PFS was 17.7 months (95% confidence interval [CI]: 4.9-22.6 months). Following initial therapy, age ≥ 40 had improved PFS on univariate analysis ( = 0.03). All patients had local recurrence, with 15 undergoing salvage surgical resections and 16 undergoing salvage radiation treatments (mostly stereotactic radiosurgery [SRS]). The median PFS was 59.2 months (95% CI: 4.0-99.3 months) after salvage surgery, 58.4 months (95% CI: 25.9-195 months) after salvage radiation, and 58.4 months (95% CI: 25.9.0-98.4 months) combined. Overall survival for the total cohort was 98.7% ± 1.7% at 2 years and 92.8% ± 5.5% at 5 years. Salvage treatments were well-tolerated with two patients (11%) reporting tinnitus and one patient each (6%) reporting headaches, visual field deficits, hearing loss, anosmia, dysphagia, or memory loss. Refractory skull base chordomas present a challenging treatment dilemma. Repeat surgical resection or SRS seems to provide adequate salvage therapy that is well-tolerated when treated at a tertiary center offering multimodality care.
脊索瘤是具有局部侵袭性的肿瘤,其特点是在初始多模式治疗后有较高的复发率。我们研究了复发性/进展性颅底脊索瘤挽救治疗的结果。
这是对一家城市三级学术医疗中心复发性/进展性颅底脊索瘤的回顾性研究。评估的结果包括总生存期、无进展生存期(PFS)和新毒性的发生率。
连续纳入18例接受≥1个疗程治疗的患者(35.3%接受挽救性手术,23.5%接受挽救性放疗,41.2%两者均接受)。中位随访时间为98.6个月(范围16 - 215个月)。初始治疗后,中位PFS为17.7个月(95%置信区间[CI]:4.9 - 22.6个月)。初始治疗后,单因素分析显示年龄≥40岁患者的PFS有所改善(P = 0.03)。所有患者均有局部复发,15例接受了挽救性手术切除,16例接受了挽救性放疗(大多为立体定向放射外科手术[SRS])。挽救性手术后的中位PFS为59.2个月(95% CI:4.0 - 99.3个月),挽救性放疗后的中位PFS为58.4个月(95% CI:25.9 - 195个月),联合治疗后的中位PFS为58.4个月(95% CI:25.9 - 98.4个月)。整个队列的2年总生存率为98.7%±1.7%,5年总生存率为92.8%±5.5%。挽救治疗耐受性良好,2例患者(11%)报告有耳鸣,各有1例患者(6%)报告有头痛、视野缺损、听力丧失、嗅觉丧失、吞咽困难或记忆力减退。
难治性颅底脊索瘤带来了具有挑战性的治疗难题。重复手术切除或SRS似乎能提供充分的挽救治疗,在提供多模式治疗的三级中心进行治疗时耐受性良好。