Coakham H B, Kemshead J T
Department of Neurological Surgery, Frenchay Health Care Trust and University of Bristol, Frenchay Hospital, UK.
J Neurooncol. 1998 Jun-Jul;38(2-3):225-32. doi: 10.1023/a:1005996606073.
Between 1984 and 1993, monoclonal antibodies (MAbs) radiolabelled with (131)I were administered into the CSF of 52 patients with neoplastic meningitis (meningosis) with progressive disease despite active conventional therapy. Selection of MAbs was based on immunoreactivity with patients' tumour and lack of binding to normal central nervous system (CNS) tissue. Following full clinical assessment and neuro-imaging which included isotope flow study of CSF pathways, (131)I-MAb was administered via a ventricular access device, lumbar catheter or both. Radioisotope activity varied from 25 mCi to 160 mCi in adults. Dose escalation was carried out and some patients received multiple doses. Distribution of (131)I-MAb and clearance kinetics were derived from serial scintigraphy and CSF/blood sampling. Evidence of localisation to tumour was frequently observed. Toxicity was minimal and easily treated, although one death occurred, possibly due to a seizure. The best results were obtained in primitive neuroectodermal tumour (n=22), where 53% of evaluable cases had responses and 11% had stable disease, adults responding better than children. Three exceptional survivals have been recorded; one patient leads a normal life at 10 years 11 months, one case is alive and normal at 3 years, 2 months. A third case survived in good condition for 8 years. The mean survival of responders was 39 months and non-responders 4 months. In the total series, 50% of patients survived for at least one year with 2 long term survivors. CSF therapy with (131)I-MAb appears to be valuable as a single agent or when used in combination with other modalities. Results of treating leukaemia and carcinoma cases suggest that re-seeding into the CSF compartment from active systemic disease may account for early relapse in the CNS. One carcinoma case with no apparent systemic disease made a remarkable response and survival for 4 years following a single treatment. Neoplastic meningitis generally carries a dismal prognosis. The results obtained in this initial trial are sufficiently encouraging to stimulate further attempts at CSF therapy with (131)I-MAbs.
1984年至1993年间,将用¹³¹I标记的单克隆抗体(MAb)注入52例患有肿瘤性脑膜炎(脑膜病变)的患者脑脊液中,这些患者尽管接受了积极的传统治疗,但病情仍在进展。单克隆抗体的选择基于其与患者肿瘤的免疫反应性以及与正常中枢神经系统(CNS)组织无结合。在进行全面临床评估和神经影像学检查(包括脑脊液通路的同位素流量研究)后,通过脑室通路装置、腰椎导管或两者同时注入¹³¹I-MAb。成人的放射性同位素活性在25毫居里至160毫居里之间。进行了剂量递增,一些患者接受了多剂治疗。¹³¹I-MAb的分布和清除动力学通过连续闪烁扫描和脑脊液/血液采样得出。经常观察到其在肿瘤部位的定位证据。毒性极小且易于治疗,尽管有1例死亡,可能是由于癫痫发作。在原始神经外胚层肿瘤(n = 22)中取得了最佳结果,其中53%的可评估病例有反应,11%病情稳定,成人的反应优于儿童。记录到3例特殊存活病例;1例患者在10年11个月时过着正常生活,1例在3年2个月时存活且状况正常。第3例病例状况良好地存活了8年。有反应者的平均生存期为39个月,无反应者为4个月。在整个系列中,50%的患者存活至少一年,有2例长期存活者。用¹³¹I-MAb进行脑脊液治疗作为单一药物或与其他方式联合使用似乎很有价值。治疗白血病和癌病例的结果表明,活跃的全身性疾病重新种植到脑脊液腔可能是中枢神经系统早期复发的原因。1例无明显全身性疾病的癌病例在单次治疗后有显著反应并存活了4年。肿瘤性脑膜炎通常预后不佳。在这项初步试验中获得的结果足以令人鼓舞,以刺激进一步尝试用¹³¹I-MAb进行脑脊液治疗。