Spreafico Filippo, Gandola Lorenza, Marchianò Alfonso, Simonetti Fabio, Poggi Geraldina, Adduci Anna, Clerici Carlo Alfredo, Luksch Roberto, Biassoni Veronica, Meazza Cristina, Catania Serena, Terenziani Monica, Musumeci Renato, Fossati-Bellani Franca, Massimino Maura
Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Int J Radiat Oncol Biol Phys. 2008 Mar 15;70(4):1011-9. doi: 10.1016/j.ijrobp.2007.07.2377. Epub 2007 Sep 27.
Brain necrosis or other subacute iatrogenic reactions has been recognized as a potential complication of radiotherapy (RT), although the possible synergistic effects of high-dose chemotherapy and RT might have been underestimated.
We reviewed the clinical and radiologic data of 49 consecutive children with malignant brain tumors treated with high-dose thiotepa and autologous hematopoietic stem cell rescue, preceded or followed by RT. The patients were assessed for neurocognitive tests to identify any correlation with magnetic resonance imaging (MRI) anomalies.
Of the 49 children, 18 (6 of 25 with high-grade gliomas and 12 of 24 with primitive neuroectodermal tumors) had abnormal brain MRI findings occurring a median of 8 months (range, 2-39 months) after RT and beginning to regress a median of 13 months (range, 2-26 months) after onset. The most common lesion pattern involved multiple pseudonodular, millimeter-size, T1-weighted unevenly enhancing, and T2-weighted hyperintense foci. Four patients with primitive neuroectodermal tumors also had subdural fluid leaks, with meningeal enhancement over the effusion. One-half of the patients had symptoms relating to the new radiographic findings. The MRI lesion-free survival rate was 74%+/-6% at 1 year and 57%+/-8% at 2 years. The number of marrow ablative courses correlated significantly to the incidence of radiographic anomalies. No significant difference was found in intelligent quotient scores between children with and without radiographic changes.
Multiple enhancing cerebral lesions were frequently seen on MRI scans soon after high-dose chemotherapy and RT. Such findings pose a major diagnostic challenge in terms of their differential diagnosis vis-à-vis recurrent tumor. Their correlation with neurocognitive results deserves further investigation.
脑坏死或其他亚急性医源性反应已被公认为放射治疗(RT)的一种潜在并发症,尽管高剂量化疗和RT可能存在的协同作用可能被低估了。
我们回顾了49例连续接受高剂量噻替哌和自体造血干细胞挽救治疗的儿童恶性脑肿瘤患者的临床和放射学数据,这些治疗在RT之前或之后进行。对患者进行神经认知测试,以确定与磁共振成像(MRI)异常的任何相关性。
在49例儿童中,18例(25例高级别胶质瘤中的6例和24例原始神经外胚层肿瘤中的12例)在RT后中位8个月(范围2 - 39个月)出现脑MRI异常,发病后中位13个月(范围2 - 26个月)开始消退。最常见的病变模式包括多个伪结节状、毫米大小、T1加权不均匀强化和T2加权高信号灶。4例原始神经外胚层肿瘤患者还出现硬膜下液漏,积液上方脑膜强化。一半的患者有与新的影像学发现相关的症状。MRI无病变生存率在1年时为74%±6%,在2年时为57%±8%。骨髓消融疗程数与影像学异常的发生率显著相关。有影像学改变和无影像学改变的儿童之间智商得分无显著差异。
高剂量化疗和RT后不久,MRI扫描经常可见多个强化性脑病变。这些发现就其与复发性肿瘤的鉴别诊断而言构成了重大诊断挑战。它们与神经认知结果的相关性值得进一步研究。