Massimino M, Simonetti F, Balestrini M R, Spreafico F, La Spina M, Terenziani M, Gandola L
Neuro-Oncology Functional Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori, Via Venezian 1, I-20133, Milan, Italy.
Neurol Sci. 2006 Jun;27(2):110-3. doi: 10.1007/s10072-006-0609-8.
Childhood intrinsic brain-stem gliomas have a dismal prognosis. Different treatment strategies have been adopted over the years without changing the final outcome of this ominous disease. Due to this grim prognosis, experimental therapeutic designs are worthwhile. Vinorelbine is a semi-synthetic vinca alkaloid that has demonstrated a broad spectrum of activity both in in vitro and in vivo experimental systems. By adopting vinorelbine during and after focal radiotherapy in the last two years, we have tried to evocate its known synergistic effect in brain-stem tumour control. Vinorelbine was administered intravenously before, during and after radiotherapy on tumour bed for a total duration of 10 months. All the consecutive patients whose clinical and radiological features corresponded to the diagnosis of an intrinsic brain-stem tumour, i.e., diffuse pontine glioma, have been accrued to this treatment protocol since July 2002. A histological assessment was not required. All patients were treated during hospital stay or in the outpatient clinic at the Istituto Nazionale Tumori of Milan (n=12) and at the Pediatric Clinic of Policlinico in Catania (n=1). Two of the thirteen patients so far treated have developed multiple subsequent, and transitory, episodes of monolateral peripheral facial nerve palsy during vinorelbine administration. The palsy always completely and spontaneously resolved at a short interval-around 30 min-after the end of the drug infusion. Obvious tumour progression was excluded by means of MRI; therefore the drug was administered as scheduled until the end of the treatment. We describe possible neurological and oncological implications of this unusual side effect, until now not reported in any other series dealing with vinorelbine as adjuvant treatment.
儿童脑干原发性胶质瘤预后不佳。多年来采用了不同的治疗策略,但并未改变这种凶险疾病的最终结局。鉴于这种严峻的预后情况,实验性治疗设计是值得的。长春瑞滨是一种半合成的长春花生物碱,在体外和体内实验系统中均显示出广泛的活性。在过去两年中,我们在局部放疗期间及之后采用长春瑞滨,试图激发其在脑干肿瘤控制方面已知的协同作用。长春瑞滨在放疗前、放疗期间及放疗后在肿瘤床部位进行静脉给药,总疗程为10个月。自2002年7月起,所有临床和影像学特征符合脑干原发性肿瘤诊断(即弥漫性脑桥胶质瘤)的连续患者均纳入该治疗方案。无需进行组织学评估。所有患者均在米兰国家肿瘤研究所(n = 12)和卡塔尼亚综合医院儿科门诊(n = 1)住院或门诊接受治疗。在目前接受治疗的13例患者中,有2例在使用长春瑞滨期间出现了多次随后的、短暂的单侧周围性面神经麻痹发作。麻痹总是在药物输注结束后短时间内(约30分钟)完全自发缓解。通过磁共振成像(MRI)排除了明显的肿瘤进展;因此,药物按计划给药直至治疗结束。我们描述了这种不寻常副作用可能的神经学和肿瘤学影响,此前在任何其他将长春瑞滨作为辅助治疗的系列报道中均未提及。