Pathological perspectives in pilocytic astrocytomas: Extent of resection as the sole critical factor for recurrence-free survival, and the challenge of evaluating conclusions derived from limited data.

Q3 Medicine
Free neuropathology Pub Date : 2023-10-20 eCollection Date: 2023-01-01 DOI:10.17879/freeneuropathology-2023-5116
Ibrahim Kulac, Irem Yenidogan, Banu Oflaz Sozmen, Arzu Baygul, Soonmee Cha, Melike Pekmezci, Tarik Tihan
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引用次数: 0

Abstract

Introduction: Pilocytic astrocytoma (PA) is one of the most common primary intracranial neoplasms in childhood with an overall favorable prognosis. Despite decades of experience, there are still diagnostic and treatment challenges and unresolved issues regarding risk factors associated with recurrence, most often due to conclusions of publications with limited data. We analyzed 499 patients with PA diagnosed in a single institution over 30 years in order to provide answers to some of the unresolved issues. Materials and Methods: We identified pilocytic astrocytomas diagnosed at the University of California, San Francisco, between 1989 and 2019, confirmed the diagnoses using the WHO 2021 essential and desirable criteria, and performed a retrospective review of the demographic and clinical features of the patients and the radiological, pathologic and molecular features of the tumors. Results: Among the patients identified from pathology archives, 499 cases fulfilled the inclusion criteria. Median age at presentation was 12 years (range 3.5 months - 73 years) and the median follow-up was 78.5 months. Tumors were predominantly located in the posterior fossa (52.6%). There were six deaths, but there were confounding factors that prevented a clear association of death to tumor progression. Extent of resection was the only significant factor for recurrence-free survival. Recurrence-free survival time was 321.0 months for gross total resection, compared to 160.9 months for subtotal resection (log rank, p <0.001). Conclusion: Multivariate analysis was able to identify extent of resection as the only significant variable to influence recurrence-free survival. We did not find a statistically significant association between age, NF1 status, tumor location, molecular alterations, and outcome. Smaller series with apparently significant results may have suffered from limited sample size, limited variables, acceptance of univariate analysis findings as well as a larger p value for biological significance. PA still remains a predominantly surgical disease and every attempt should be made to achieve gross total resection since this appears to be the most reliable predictor of recurrence-free survival.

毛细胞星形细胞瘤的病理学观点:切除程度是无复发生存的唯一关键因素,以及评估有限数据得出的结论的挑战。
毛细胞星形细胞瘤(PA)是儿童最常见的原发性颅内肿瘤之一,预后良好。尽管有几十年的经验,但在与复发相关的风险因素方面,仍然存在诊断和治疗方面的挑战和未解决的问题,这通常是由于数据有限的出版物得出的结论。我们分析了30年来在一家机构诊断的499名PA患者,以便为一些尚未解决的问题提供答案。材料和方法:我们确定了1989年至2019年间在加州大学旧金山分校诊断的毛细胞星形细胞瘤,使用世界卫生组织2021基本和理想标准确认了诊断,并对患者的人口统计学和临床特征以及肿瘤的放射学、病理学和分子特征进行了回顾性审查。结果:在从病理档案中确定的患者中,499例符合纳入标准。出现时的中位年龄为12岁(3.5个月至73岁),中位随访时间为78.5个月。肿瘤主要位于后颅窝(52.6%)。有6例死亡,但有一些混杂因素阻止了死亡与肿瘤进展的明确关联。切除程度是无复发生存率的唯一重要因素。全切除无复发生存期321.0个月,与160.9个月的次全切除相比(log-rank,p结论:多变量分析能够确定切除程度是影响无复发生存率的唯一显著变量。我们没有发现年龄、NF1状态、肿瘤位置、分子改变和结果之间存在统计学上显著的相关性。具有明显显著结果的较小系列可能受到样本量有限、糖尿病,接受单变量分析结果以及较大的生物学意义p值。PA仍然是一种主要的外科疾病,应该尽一切努力实现全切除,因为这似乎是无复发生存率的最可靠预测指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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