Cancer Metastases Prevention by Photodynamic In-vivo Detection and Destruction of Circulating Tumor Cell Clusters

D. Schikora, Michael Weber
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引用次数: 1

Abstract

We demonstrate a new diagnostic method, the Photodynamic Infrared Spectroscoppy (PDIS), which is able to detect circulating tumor clusters and circulating tumor cells in the circulatory system. In particular the circulating tumor clusters are agreed as the main cause for metastases formation and therefore for the cancer mortality. The cancer mortality rate is unchanged worldwide in the last twenty years, indicating the absence of clinically effective metastases prevention therapies. No diagnostic method is existing, which allows to detect tumor clusters in vivo in the blood, which is the prerequisite for tumor cluster destruction and metastases prevention. The PDIS method is based on photodynamic physics and high resolution spectroscopy and is using calibrated spectroscopic data for the diagnostic analysis of the blood screening spectra. In the paper we are focussing to brest cancer diagnostics using the photosensitizer Indocyangreen. A flow appartus is described, which enables to calibrate the fluorescence spectra of single tumor cells and single tumor clusters. Due to the calibrated diagnostic data, the PDIS enables the identification of circulating tumot cells and tumor clusters in the bloodstream with the ultimate accuracy of one cluster per 6 l blood and with a sensitivity of 98%. Circulating tumor cell clusters are formed only in solid tumors, that’s why they are appropriate objects to validate cancer treatments and to recognice cancer formation. Due to the one-to one correspondence between tumor clusters in blood and the existence of solid tumors in the organism, the PDIS as diagnostic method can be used to control and to verify any oncologic treatment with respect to its clinical efficay. The common "wait and hope" strategy after finishing a chemotheraypy can be replaced by an effective follow-up strategy. Furthermore, the PDIS diagnostics can be used to recognize a tumor formation in the earliest possible stage, the carcinom in-situ stage. Finally the in-vivo detection of tumor clusters in the blood enables the immediate and controlled destruction of the these clusters by Photodynamic Therapy or other oncologic methods and therefore an increase of the overall survival of cancer patients and a decrease of the cancer mortalitay rate.
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通过光动力学体内检测和破坏循环肿瘤细胞簇来预防癌症转移
我们展示了一种新的诊断方法,光动力红外光谱(PDIS),它能够检测循环系统中的循环肿瘤簇和循环肿瘤细胞。特别是循环肿瘤集群被认为是转移形成的主要原因,因此是癌症死亡率的主要原因。在过去的二十年里,世界范围内的癌症死亡率没有变化,这表明缺乏临床有效的转移预防疗法。目前还没有一种诊断方法能够在血液中检测到体内的肿瘤簇,而这是破坏肿瘤簇和预防肿瘤转移的前提。PDIS方法基于光动力物理和高分辨率光谱学,并使用校准的光谱数据对血液筛查光谱进行诊断分析。在本文中,我们的重点是乳腺癌诊断使用光敏剂indocyanggreen。描述了一种能够校准单个肿瘤细胞和单个肿瘤簇的荧光光谱的流动装置。由于经过校准的诊断数据,PDIS能够识别血液中的循环肿瘤细胞和肿瘤簇,最终准确度为每6 l血液一个簇,灵敏度为98%。循环肿瘤细胞团只在实体肿瘤中形成,这就是为什么它们是验证癌症治疗和识别癌症形成的合适对象。由于血液中的肿瘤簇与机体中实体肿瘤的存在是一一对应的,PDIS作为一种诊断方法,可用于控制和验证任何肿瘤治疗的临床疗效。化疗结束后常见的“等待和希望”策略可以被有效的随访策略所取代。此外,PDIS诊断可用于识别肿瘤形成在尽可能早的阶段,癌原位阶段。最后,血液中肿瘤簇的体内检测能够通过光动力疗法或其他肿瘤学方法对这些簇进行即时和可控的破坏,从而提高癌症患者的总体生存率,降低癌症死亡率。
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