Rodot S, Darcourt J, Bussière F, Lacour J P, Migneco O, Thyss A, Michelot J M, Bonafous J F, Schneider M, Barety M
Department of Dermatology, Hôpital Pasteur, Nice, France.
Melanoma Res. 1994 Oct;4(5):307-12. doi: 10.1097/00008390-199410000-00007.
123I-N-(di-ethylamino-2-ethyl) 4 iodobenzamide (I-BZA) has been put forward by the Clermont-Ferrand INSERM U71 group (France) as a tracer for malignant melanoma. We report on the clinical results obtained in 56 studies performed on 48 patients. Whole body scans along with spot views were obtained after injection of 185 MBq of I-BZA. The scans were read by three independent observers and correlated to the clinical findings and the other imaging modalities available, taking into account all lesions larger than 1 cm. Patients were classified into two groups on the basis of a post-treatment survey of patients: group I, in complete remission (24 scans); group II: documented metastases (32 scans). In group 1, 21 studies were truly negative. However, three studies showed positive results. Only one turned out to be a false positive (specificity 95%), the other two revealed unknown lesions and modified the patients' management. In group II, 73% of the known metastases were detected with higher sensitivities (> 80%) for eye and orbit, lung and abdomen. One false positive was reported and four new lesions were detected. I-BZA scintigraphy has the same sensitivity as immunoscintigraphy with higher specificity and without the risk of xenoimmunization. It is a useful tool for staging malignant melanoma which can improve patient management.
法国克莱蒙费朗国家健康与医学研究院U71组提出将123I-N-(二乙氨基-2-乙基)4碘苯甲酰胺(I-BZA)作为恶性黑色素瘤的示踪剂。我们报告了对48例患者进行的56项研究的临床结果。注射185MBq的I-BZA后进行全身扫描及局部显像。由三名独立观察者解读扫描结果,并与临床发现及其他可用的成像方式进行关联,将所有大于1cm的病变纳入考虑。根据对患者的治疗后调查,将患者分为两组:第一组,完全缓解(24次扫描);第二组:有记录的转移(32次扫描)。在第一组中,21项研究结果真正为阴性。然而,有三项研究显示为阳性结果。只有一项结果为假阳性(特异性95%),另外两项发现了未知病变并改变了患者的治疗方案。在第二组中,73%的已知转移灶被检测到,对眼和眼眶、肺及腹部的检测灵敏度较高(>80%)。报告了一项假阳性结果,并检测到四个新病变。I-BZA闪烁扫描与免疫闪烁扫描具有相同的灵敏度,但特异性更高,且没有异种免疫的风险。它是恶性黑色素瘤分期的一种有用工具,可改善患者的治疗管理。