Department of Pediatric Oncology, St. Hedwig Children's Hospital, University of Regensburg, Regensburg, Germany.
Institute of Neuropathology, University Hospital Münster, Münster, Germany.
J Neurooncol. 2009 Dec;95(3):383-392. doi: 10.1007/s11060-009-9936-y. Epub 2009 Jun 20.
Atypical choroid plexus papilloma (APP) represents a novel intermediate-grade subtype of choroid plexus tumor (CPT), the clinical outcome of which has not been described yet. We present the first analysis of a group of APP patients enrolled in the ongoing CPT-SIOP-2000 study of CPTs. A worldwide registration and a randomized trial for those patients who require chemotherapy started in 2000. For APP, maximal surgical resection was recommended. After surgery, patients who had undergone complete resection were observed, whereas patients with incompletely resected or metastasized APP were treated with six chemotherapy courses (etoposide and vincristine, combined with either carboplatin or cyclophosphamide). Risk-adapted radiotherapy was given only to patients older than 3 years of age. Of the 106 patients with a centrally confirmed CPT histology, 30 had APP, 42 CPP and 34 CPC. APP patients were significantly younger (median = 0.7 years) than patients with CPP or CPC (both medians = 2.3 years). Complete resection was achieved in 68 (64%) patients (79% in CPP, 63% in APP, and 47% in CPC). Metastases were present at diagnosis in 17% of APP patients, 5% of CPP patients, and 21% of CPC patients. All nine APP patients who received postoperative chemotherapy showed an early response after two cycles: two had complete remission, four had partial response, and three had stable disease. In the observation group of 15 patients, one event was seen, and all patients were alive. In the treatment group, one patient with a metastasized tumor and incompletely resected APP died. While APP was defined histologically, median percentages of both the Ki-67/MIB-1 proliferation marker and the p53 tumor suppressor protein increased across the three histological subtypes (from CPP to APP and then CPC), suggesting that the subtypes comprise an ordinal categorization of increasingly severe CPT tumors. This ordering was reiterated by clinical outcome in the 92 patients treated per the study protocol, with 5-year EFS rates of 92% in 39 CPP patients, 83% in 24 APP patients, and 28% in 29 CPC patients. A similar ordering was seen when all 106 patients were evaluated for EFS. APP responded favorably to chemotherapy. The intermediate position of APP between CPP and CPC was supported by the clinical data.
非典型脉络丛乳头状瘤(APP)是一种新型的脉络丛肿瘤(CPT)中级别亚型,其临床结果尚未描述。我们报告了正在进行的 CPT-SIOP-2000 研究中一组 APP 患者的首次分析。该研究于 2000 年开始对需要化疗的 CPT 患者进行全球注册和随机试验。对于 APP,建议进行最大程度的手术切除。手术后,对完全切除的患者进行观察,而对不完全切除或转移的 APP 患者进行 6 个化疗疗程(依托泊苷和长春新碱,与卡铂或环磷酰胺联合使用)。只有年龄大于 3 岁的患者才给予风险适应放疗。在 106 例经中枢确认的 CPT 组织学患者中,30 例为 APP,42 例为 CPP,34 例为 CPC。APP 患者明显比 CPP 或 CPC 患者年轻(中位数=0.7 岁)(中位数均为 2.3 岁)。68 例(64%)患者实现了完全切除(CPP 为 79%,APP 为 63%,CPC 为 47%)。诊断时存在转移的 APP 患者占 17%,CPP 患者占 5%,CPC 患者占 21%。接受术后化疗的 9 例 APP 患者在两个周期后均表现出早期反应:2 例完全缓解,4 例部分缓解,3 例疾病稳定。在 15 例观察患者中,仅观察到 1 例事件,所有患者均存活。在治疗组中,1 例转移性肿瘤和不完全切除的 APP 患者死亡。虽然根据组织学定义了 APP,但三种组织学亚型(从 CPP 到 APP 再到 CPC)的 Ki-67/MIB-1 增殖标志物和 p53 肿瘤抑制蛋白的百分比均增加,这表明这些亚型构成了严重程度递增的 CPT 肿瘤的有序分类。这一排序在 92 例按研究方案治疗的患者的临床结果中得到了重复,39 例 CPP 患者的 5 年 EFS 率为 92%,24 例 APP 患者为 83%,29 例 CPC 患者为 28%。对所有 106 例患者进行 EFS 评估时也观察到了类似的排序。APP 对化疗反应良好。APP 在 CPP 和 CPC 之间的中间位置得到了临床数据的支持。