Dirven C M, Mooij J J, Molenaar W M
Department of Neurosurgery, Free University Hospital, Amsterdam, The Netherlands.
Childs Nerv Syst. 1997 Jan;13(1):17-23. doi: 10.1007/s003810050033.
In a retrospective study of 73 patients operated on for cerebellar pilocytic astrocytomas, results of treatment, outcome and biological behaviour of residual tumour were analysed. Complete tumour resection proven by CT or MRI scans within 1 year after surgery was achieved only in 69% of cases. In 31% of cases the surgeon's opinion on the extent of surgical resection was not borne out by the result of postoperative neuroimaging. Progression of residual tumour or tumour recurrence appeared in 19% of patients. 1 patient showed metastatic spread along the craniospinal axis, and in 1 patient malignant degeneration appeared during follow-up. Stable residual tumour or regression of residual tumour was seen in 14% of patients. Outcome after surgical treatment, which was combined with irradiation in 10 patients (14%), was favourable in 80% and unfavourable in 20% of patients. This outcome of treatment was not influenced by a second operation for progression of residual tumour or recurrent tumour. Characteristics of patients with tumour progression after the first operation did not differ from those of the whole group. There were 17 reoperations for residual or recurrent tumour, 10 of which took place within 4 years after the initial surgical treatment. Surgery-related morbidity was 15% and mortality 4%. Irradiation to residual tumour in 8 patients was followed by complete regression in 1 patient, progression in 4 patients and no changes in 1 patient. For the remaining 2 patients the effect of irradiation on the residual tumour is unknown. Factors that determine the prognosis are discussed on the basis of this retrospective analysis and the data from the literature. It is concluded that optimal treatment for a cerebellar pilocytic astrocytoma does not consist solely in surgery with the aim of total tumour removal and careful tumour handling in order to avoid spread of tumour cells and subsequent metastases and additional radiation therapy is strictly selected cases, but also in posttreatment follow-up based on direct postoperative neuroimaging, preferably by MRI. An algorithm for postoperative follow-up management is presented.
在一项对73例接受小脑毛细胞型星形细胞瘤手术治疗患者的回顾性研究中,分析了治疗结果、预后以及残留肿瘤的生物学行为。术后1年内通过CT或MRI扫描证实实现完全肿瘤切除的病例仅占69%。在31%的病例中,术后神经影像学结果与外科医生对手术切除范围的判断不符。19%的患者出现残留肿瘤进展或肿瘤复发。1例患者沿颅脊髓轴出现转移扩散,1例患者在随访期间出现恶性变。14%的患者残留肿瘤稳定或残留肿瘤缩小。10例患者(14%)接受了手术联合放疗,手术治疗后的预后在80%的患者中良好,20%的患者预后不佳。这种治疗结果不受因残留肿瘤进展或复发性肿瘤而进行的二次手术影响。首次手术后肿瘤进展患者的特征与整个研究组患者的特征无差异。因残留或复发性肿瘤进行了17次再次手术,其中10次在初次手术治疗后4年内进行。手术相关发病率为15%,死亡率为4%。8例患者对残留肿瘤进行放疗,其中1例患者放疗后完全缓解,4例患者肿瘤进展,1例患者无变化。其余2例患者放疗对残留肿瘤的影响未知。基于这项回顾性分析和文献数据讨论了决定预后的因素。得出的结论是,小脑毛细胞型星形细胞瘤的最佳治疗方案不仅包括以完全切除肿瘤为目的的手术以及谨慎处理肿瘤以避免肿瘤细胞扩散和随后的转移,在严格选择的病例中还包括额外的放射治疗,而且还包括基于术后直接神经影像学检查(最好是MRI)的治疗后随访。本文提出了术后随访管理的算法。