Tc-99m标记(N2S2)抗黑色素瘤抗体片段和单光子发射计算机断层扫描的临床经验。

R L Wahl, N A Swanson, J W Johnson, R Natale, N A Petry, S Mallette, S Kasina, J Reno, K Sullivan, P Abrams
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引用次数: 0

摘要

我们在12例临床II期和III期黑色素瘤患者中评估了小鼠tc -99m标记的抗黑色素瘤Fab片段的成像能力。Tc-99m-NRX118.7抗黑色素瘤Fab片段,10.0 ~ 27.2 mCi (370- 1,006 MBq),在不相关的非特异性完整抗体后30分钟注射,在给予完整的特异性抗体后5分钟注射。所有患者均进行全身扫描和局部观察。另外对8例患者行单光子发射计算机断层扫描(SPECT)。手术耐受性良好,38个已知黑色素瘤灶中有31个被检测到(敏感性82%)。SPECT有助于检测和更好地定位头部、颈部和胸部的病变。在了解正常的锝-99m活性的聚集和排泄部位(如肾脏和肠道)的情况下,进行解释时,该技术的特异性令人满意。在一些病例中,病变是通过抗体扫描在其他方法检测之前发现的,在两个病例中,可触及肿块的抗体扫描缺乏可视化,正确地表明肿块中没有黑色素瘤存在。3例患者的扫描结果导致患者护理的改变;包括防止积极的手术和非手术治疗。虽然这些数据令人鼓舞,但在其他患者中进行评估对于确定这种抗体扫描在黑色素瘤患者管理中的临床应用至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical experience with Tc-99m labeled (N2S2) anti-melanoma antibody fragments and single photon emission computed tomography.

We evaluated the imaging capability of murine Tc-99m-labeled antimelanoma Fab fragments in 12 patients with clinical stage II and III melanoma. Tc-99m-NRX118.7 antimelanoma Fab fragment, 10.0 to 27.2 mCi (370-1, 006 MBq), was injected IV 30 min after irrelevant nonspecific intact antibody and 5 min after intact specific antibody were given. In all patients, whole-body scans and spot views were obtained. Single photon emission computed tomography (SPECT) was additionally performed in eight of the patients. The procedure was well tolerated, and 31 of 38 known foci of melanoma were detected (sensitivity, 82%). SPECT aided in detecting and better localizing lesions in the head, neck, and chest. The specificity of the technique was satisfactory when interpretation was performed with a knowledge of normal sites of accretion and excretion of technetium-99m activity such as the kidneys and gut. In several instances, lesions were discovered by means of the antibody scan before detection by other methods, and in two instances, the lack of visualization on antibody scan of a palpable mass correctly indicated that no melanoma was present in the mass. Scan results in three patients led to alterations in patient care; including preventing aggressive surgical and nonsurgical treatments. Although these data are encouraging, evaluation in additional patients will be essential to determine the clinical utility of this antibody scan in the management of patients with melanoma.

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