Graffeo Christopher S, Perry Avital, Raghunathan Aditya, Kroneman Trynda N, Jentoft Mark, Driscoll Colin L, Neff Brian A, Carlson Matthew L, Jacob Jeffrey, Link Michael J, Van Gompel Jamie J
Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota, United States.
Department of Laboratory Medicine & Pathology, Mayo Clinic, Rochester, Minnesota, United States.
J Neurol Surg B Skull Base. 2018 Oct;79(5):482-488. doi: 10.1055/s-0038-1627474. Epub 2018 Feb 7.
Vestibular schwannoma (VS) behavior following subtotal resection (STR) is highly variable. Overall progression rates have been reported as high as 44%, and optimal treatment is controversial. Correspondingly, identification of a reliable clinical or pathologic marker associated with progression after STR would help guide decision-making. A prospectively maintained institutional VS registry from 1999 to 2014 was retrospectively reviewed for sporadic VS patients who underwent primary STR without preceding stereotactic radiosurgery (SRS) by a single neurosurgery-neurotology team. Primary endpoints included tumor progression and postoperative facial nerve function. Pathologic specimens were stained for Ki67, CD68, S100, and SOX10 and were quantitated by digital imaging analysis. was defined as the ratio of CD68 macrophages to S100 macrophages and Schwannian tumor cells. Clinical outcomes were correlated with pathologic markers. Forty-six patients met the study inclusion criteria. Thirteen (28%) progressed during a mean 57 months of follow-up (range 15-149). Favorable postoperative facial nerve function (House-Brackmann I-II) was achieved in 37 (80%). CD68 cells were present at significantly higher concentrations in tumors that progressed ( = 0.03). Higher was significantly associated with both tumor progression ( = 0.02) and unfavorable facial nerve function ( = 0.02). Ki67 percent positivity was not significantly associated with either primary endpoint ( = 0.83; = 0.58). may provide an important marker for individuals at the highest risk for progression of VS after STR, potentially prompting closer surveillance or consideration for upfront SRS following STR. This finding supports preceding conclusions that an intratumoral macrophage-predominant inflammatory response may be a marker for tumor growth and a potential therapeutic target.
次全切除(STR)后前庭神经鞘瘤(VS)的行为具有高度变异性。据报道,总体进展率高达44%,最佳治疗方法存在争议。相应地,识别与STR后进展相关的可靠临床或病理标志物将有助于指导决策。 对1999年至2014年前瞻性维护的机构VS登记册进行回顾性研究,纳入由单一神经外科 - 神经耳科学团队进行初次STR且未先行立体定向放射外科手术(SRS)的散发性VS患者。主要终点包括肿瘤进展和术后面神经功能。病理标本进行Ki67、CD68、S100和SOX10染色,并通过数字成像分析进行定量。 定义为CD68巨噬细胞与S100巨噬细胞及施万细胞瘤细胞的比例。临床结果与病理标志物相关。 46例患者符合研究纳入标准。在平均57个月的随访期间(范围15 - 149个月),13例(28%)出现进展。37例(80%)术后面神经功能良好(House - Brackmann I - II级)。进展的肿瘤中CD68细胞浓度显著更高( = 0.03)。较高的 与肿瘤进展( = 0.02)和不良面神经功能( = 0.02)均显著相关。Ki67阳性百分比与两个主要终点均无显著相关性( = 0.83; = 0.58)。 可能为STR后VS进展风险最高的个体提供一个重要标志物,可能促使在STR后进行更密切的监测或考虑先行SRS。这一发现支持了之前的结论,即肿瘤内以巨噬细胞为主的炎症反应可能是肿瘤生长的标志物和潜在的治疗靶点。