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首页> 外文期刊>Seminars in Nuclear Medicine >F-18 Fluoromisonidazole for Imaging Tumor Hypoxia: Imaging the Microenvironment for Personalized Cancer Therapy
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F-18 Fluoromisonidazole for Imaging Tumor Hypoxia: Imaging the Microenvironment for Personalized Cancer Therapy

机译:F-18氟亚咪唑对肿瘤缺氧的影像学:影像学微环境的个性化癌症治疗。

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Hypoxia in solid tumors is one of the seminal mechanisms for developing aggressive trait and treatment resistance in solid tumors. This evolutionarily conserved biological mechanism along with derepression of cellular functions in cancer, although resulting in many challenges, provide us with opportunities to use these adversities to our advantage. Our ability to use molecular imaging to characterize therapeutic targets such as hypoxia and apply this information for therapeutic interventions is growing rapidly. Evaluation of hypoxia and its biological ramifications to effectively plan appropriate therapy that can overcome the curelimiting effects of hypoxia provides an objective means for treatment selection and planning. Fluoromisonidazole (FMISO) continues to be the lead radiopharmaceutical in PET imaging for the evaluation, prognostication, and quantification of tumor hypoxia, one of the key elements of the tumor microenvironment. FMISO is less confounded by blood flow, and although the images have less contrast than FDG-PET, its uptake after 2 hours is an accurate reflection of inadequate regional oxygen partial pressure at the time of radiopharmaceutical administration. By virtue of extensive clinical utilization, FMISO remains the lead candidate for imaging and quantifying hypoxia. The past decade has seen significant technological advances in investigating hypoxia imaging in radiation treatment planning and in providing us with the ability to individualize radiation delivery and target volume coverage. The presence of widespread hypoxia in the tumor can be effectively targeted with a systemic hypoxic cell cytotoxin or other agents that are more effective with diminished oxygen partial pressure, either alone or in combination. Molecular imaging in general and hypoxia imaging in particular will likely become an important in vivo imaging biomarker of the future, complementing the traditional direct tissue sampling methods by providing a snap shot of a primary tumor and metastatic disease and in following treatment response and will serve as adjuncts to personalized therapy. Published by Elsevier Inc.
机译:实体瘤中的缺氧是在实体瘤中发展侵略性和治疗抗性的重要机制之一。尽管导致许多挑战,但这种在进化上保守的生物学机制以及细胞功能在癌症中的阻遏,为我们提供了利用这些逆境发挥优势的机会。我们使用分子成像表征诸如低氧等治疗目标并将这些信息应用于治疗干预的能力正在迅速增长。评估缺氧及其生物学影响以有效计划可克服缺氧的局限性治疗的适当治疗方法,为治疗选择和计划提供了客观的手段。氟亚甲基咪唑(FMISO)继续是PET成像中的主要放射性药物,用于评估,预后和量化肿瘤缺氧(肿瘤微环境的关键要素之一)。 FMISO受血流的干扰较小,尽管图像的对比度低于FDG-PET,但2小时后摄取的图像可以准确反映出放射性药物给药时区域氧分压不足。由于广泛的临床利用,FMISO仍然是影像学和量化缺氧的主要候选对象。在过去的十年中,在研究放射治疗计划中的低氧成像以及为我们提供个性化放射传输和目标体积覆盖范围的能力方面,已经取得了重大的技术进步。全身性缺氧细胞毒素或其他在氧分压降低时更有效的药物可以有效地靶向肿瘤中普遍存在的缺氧,无论是单独使用还是组合使用。一般的分子成像,尤其是低氧成像,将有可能成为未来重要的体内成像生物标志物,通过提供对原发性肿瘤和转移性疾病的快照以及随后的治疗反应来补充传统的直接组织采样方法,并将作为辅助个性化治疗。由Elsevier Inc.发布

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