Beer Ambros J, Niemeyer Markus, Carlsen Janette, Sarbia Mario, Nährig Jörg, Watzlowik Petra, Wester Hans-Jürgen, Harbeck Nadia, Schwaiger Markus
Department of Nuclear Medicine, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
J Nucl Med. 2008 Feb;49(2):255-9. doi: 10.2967/jnumed.107.045526. Epub 2008 Jan 16.
UNLABELLED: The integrin alpha(v)beta(3) is a key player in angiogenesis and metastasis. Our aim was to study the uptake patterns of the alpha(v)beta(3)-selective PET tracer (18)F-galacto-RGD in invasive ductal breast cancer. METHODS: Sixteen patients with primary (n = 12) or metastasized breast cancer (n = 4) were examined with (18)F-galacto-RGD PET. Standardized uptake values (SUVs) were derived by region-of-interest analysis, and immunohistochemistry of alpha(v)beta(3) expression was performed (n = 5). RESULTS: (18)F-Galacto-RGD PET identified all invasive carcinomas, with SUVs from 1.4 to 8.7 (mean +/- SD, 3.6 +/- 1.8; tumor-to-blood and tumor-to-muscle ratios, 2.7 +/- 1.6 and 6.2 +/- 2.2, respectively). Lymph-node metastases were detected in 3 of 8 patients (mean SUV, 3.3 +/- 0.8). SUVs in distant metastases were heterogeneous (2.9 +/- 1.4). Immunohistochemistry confirmed alpha(v)beta(3) expression predominantly on microvessels (5/5) and, to a lesser extent, on tumor cells (3/5). CONCLUSION: Our results suggest generally elevated and highly variable alpha(v)beta(3) expression in human breast cancer lesions. Consequently, further imaging studies with (18)F-galacto-RGD PET in breast cancer patients for assessment of angiogenesis or planning of alpha(v)beta(3)-targeted therapies are promising.
未标注:整合素α(v)β(3)是血管生成和转移中的关键因子。我们的目的是研究α(v)β(3)选择性正电子发射断层显像(PET)示踪剂(18)F-半乳糖-RGD在浸润性导管乳腺癌中的摄取模式。 方法:对16例原发性(n = 12)或转移性乳腺癌(n = 4)患者进行了(18)F-半乳糖-RGD PET检查。通过感兴趣区分析得出标准化摄取值(SUV),并进行了α(v)β(3)表达的免疫组织化学检查(n = 5)。 结果:(18)F-半乳糖-RGD PET识别出所有浸润性癌,SUV值为1.4至8.7(平均值±标准差,3.6±1.8;肿瘤与血液及肿瘤与肌肉的比值分别为2.7±1.6和6.2±2.2)。8例患者中有3例检测到淋巴结转移(平均SUV,3.3±0.8)。远处转移灶的SUV值不均一(2.9±1.4)。免疫组织化学证实α(v)β(3)主要在微血管上表达(5/5),在肿瘤细胞上表达较少(3/5)。 结论:我们的结果表明,人类乳腺癌病变中α(v)β(3)表达普遍升高且高度可变。因此,对乳腺癌患者进行进一步的(18)F-半乳糖-RGD PET成像研究以评估血管生成或规划α(v)β(3)靶向治疗具有前景。
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