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[利用¹²³I标记雌二醇进行乳腺癌肿瘤闪烁显像——受体闪烁显像]

[Tumor scintigraphy using 123I-labeled estradiol in breast cancer--receptor scintigraphy].

作者信息

Scheidhauer K, Müller S, Smolarz K, Bräutigam P, Briele B

机构信息

Kliniken und Polikliniken bzw. Instituten für Nuklearmedizin der Westfälischen Wilhelms-Universität Münster, FRG.

出版信息

Nuklearmedizin. 1991 Jun;30(3):84-99.

PMID:1871007
Abstract

The estrogen receptor (ER) status is an important factor for prognosis and endocrine therapy of breast cancer. Therefore 16-alpha-123I-iodoestradiol-17-beta (123I-E2) as a receptor-specific radiopharmacon was used for scintigraphic tumor detection in 62 patients suspected of breast cancer. The studies were performed as a multicenter trial (5 university hospitals) to validate the method and to overcome methodical problems. A fast tracer elimination from the blood pool into the liver was seen, followed by biliary excretion allowing early imaging of the thorax due to low background activity but resulting in difficult imaging conditions of the abdomen. In 42 patients (30 carcinomas, 12 benign lesions) the overall sensitivity was 66% (ER status cut-off: 10 fmol/mg). Some patients with breast cancer showed focal or diffuse uptake in the area of primary lymph drainage (parasternal, axillary) without any clinical correlation, demanding follow-up investigations. There was only one false-positive result in a receptor-negative primary carcinoma; thus, the non-invasive determination of the ER status seems to be feasible. The sensitivity of 123I-E2 in the detection of primary breast cancer or metastases and recurrences is low compared to mammography and other methods; therefore, 123I-E2 scintigraphy cannot be used as a screening method. Differentiation of malignant and benign tissue is even more difficult as both may have a positive ER status, for example in mastopathy. Nevertheless, 123I-E2 scintigraphy is an in vivo imaging technique for the detection of breast cancer depending on the ER status and provides information about tumor localisation. It may become a specific method for the non-invasive diagnosis of the ER status and may be helpful in follow-up studies. As a receptor-specific agent 123I-E2 may give answers to questions of tumor heterogeneity and changes of the ER status during therapy.

摘要

雌激素受体(ER)状态是乳腺癌预后和内分泌治疗的一个重要因素。因此,16-α-123I-碘雌二醇-17-β(123I-E2)作为一种受体特异性放射性药物,被用于对62例疑似乳腺癌患者进行肿瘤闪烁显像检测。这些研究作为一项多中心试验(5所大学医院)开展,以验证该方法并克服方法学上的问题。观察到示踪剂从血池快速清除进入肝脏,随后经胆汁排泄,这使得胸部能够因低本底活性而进行早期显像,但导致腹部的显像条件困难。在42例患者(30例癌,12例良性病变)中,总体灵敏度为66%(ER状态临界值:10 fmol/mg)。一些乳腺癌患者在原发淋巴引流区域(胸骨旁、腋窝)出现局灶性或弥漫性摄取,而无任何临床关联,需要进行随访研究。在一例受体阴性的原发性癌中仅有一个假阳性结果;因此,ER状态的非侵入性测定似乎是可行的。与乳腺X线摄影和其他方法相比,123I-E2在检测原发性乳腺癌或转移灶及复发方面的灵敏度较低;因此,123I-E2闪烁显像不能用作筛查方法。恶性和良性组织的鉴别更加困难,因为两者的ER状态都可能为阳性,例如乳腺病。尽管如此,123I-E2闪烁显像仍是一种根据ER状态检测乳腺癌的体内成像技术,并可提供有关肿瘤定位的信息。它可能成为ER状态非侵入性诊断的一种特异性方法,并且可能有助于随访研究。作为一种受体特异性药物,123I-E2可能回答肿瘤异质性以及治疗期间ER状态变化的问题。

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Images of estrogen-receptor-positive breast tumors produced by estradiol labeled with iodine I 123 at 16 alpha.用碘I 123标记的16α雌二醇产生的雌激素受体阳性乳腺肿瘤的图像。
Arch Surg. 1993 Dec;128(12):1373-81. doi: 10.1001/archsurg.1993.01420240081016.

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Breaks in DNA accompany estrogen-receptor-mediated cytotoxicity from 16 alpha[125I]iodo-17 beta-estradiol.DNA断裂伴随着16α[¹²⁵I]碘-17β-雌二醇介导的雌激素受体细胞毒性。
J Cancer Res Clin Oncol. 1993;119(4):207-14. doi: 10.1007/BF01624432.
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The role of nuclear medicine in oncology.
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