Determination of Optimal Treatment Plan for Papillary Tumor of the Pineal Region: Case Series With Literature Review.

Brandi W Pang, David J Mazur-Hart, Nasser K Yaghi, Seunggu Jude Han, Jesse J Liu
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Abstract

Background: Papillary tumor of the pineal region (PTPR) is a rare neuroepithelial tumor with Central Nervous System (CNS) World Health Organization (WHO) grade II or III classification. Due to its rarity, there is no clear census on treatment. The purpose of this study is to identify the optimal treatment plan focused on extending overall survival (OS).

Methods: This is an institutional case series with review of the literature. Fifty-three publications were analyzed. Only cases with histological diagnosis of PTPR were included. Data collected included demographics, treatment modalities, disease progression, and OS.

Results: The analysis included 105 patients from the literature and 3 new cases (54 female, 50%) with an average age of 33.1 years (range 1-73 years). The average lesion size was 26.4 mm (range 5-50 mm) in longest axis. All patients underwent an initial resection. There were 46 cases of surgery alone. The remaining cases received adjuvant therapy including radiation (RT), stereotactic radiosurgery (SRS), chemotherapy (CT), or RT and CT. The average follow-up was 61.4 months (range 1-240 months). OS at 1 year was 96.9%, at 5 years was 87.5%, and at 10 years was 80.2%. Overall progression-free survival (PFS) was 57.4%. Statistical significance was observed in PFS in the surgery plus SRS group and surgery plus CT and RT group. Surgery with SRS had the best PFS (75%), and OS at 1 year (100%) and 5 years (88.9%). Surgery with CT and RT had the best OS at 10 years (85.7%).

Conclusion: We describe a case series and literature review of PTPR to help guide the most effective treatment strategies for this rare disease entity. We recommend surgery followed by SRS as the treatment of choice because of its best PFS and 5-year survival rates. We would also recommend adding chemotherapy in the event of disease progression or recurrence as adjuvant radiation and chemotherapy provided the best 10-year survival.

确定松果体区乳头状肿瘤的最佳治疗方案:病例系列与文献综述。
背景:松果体乳头状瘤(PTPR)是一种罕见的神经上皮性肿瘤,属于世界卫生组织(WHO)中枢神经系统(CNS)II级或III级分类。由于其罕见性,目前还没有明确的治疗普查。本研究的目的是确定最佳治疗方案,重点是延长总生存期(OS):方法:这是一项机构病例系列研究,并回顾了相关文献。分析了 53 篇文献。仅纳入组织学诊断为PTPR的病例。收集的数据包括人口统计学、治疗方式、疾病进展和OS:分析包括文献中的 105 例患者和 3 例新病例(54 例女性,50%),平均年龄为 33.1 岁(1-73 岁不等)。病灶长轴平均大小为26.4毫米(范围5-50毫米)。所有患者均接受了初次切除术。其中 46 例仅接受了手术治疗。其余病例接受了辅助治疗,包括放射治疗(RT)、立体定向放射手术(SRS)、化疗(CT)或RT和CT。平均随访时间为61.4个月(1-240个月)。1年的OS为96.9%,5年的OS为87.5%,10年的OS为80.2%。总体无进展生存期(PFS)为 57.4%。手术加SRS组和手术加CT和RT组的PFS具有统计学意义。手术加SRS组的PFS(75%)、1年OS(100%)和5年OS(88.9%)最好。手术加 CT 和 RT 的 10 年 OS 最佳(85.7%):我们描述了 PTPR 的病例系列和文献综述,以帮助指导这一罕见疾病实体的最有效治疗策略。我们建议首选先手术后 SRS 的治疗方法,因为其 PFS 和 5 年生存率最佳。我们还建议在疾病进展或复发时加入化疗,因为辅助放疗和化疗可提供最佳的 10 年生存率。
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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