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(Minimal Residual Disease (MRD) in gastric carcinoma--an overview).

机译:胃癌的最小残留疾病(MRD)概述

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Despite recent developments in therapy for gastric cancer, the prognosis of this disease remains poor in advanced stages. In many cases even curatively treated patients without any residual tumour develop metachronous metastases. As in other solid tumours, adjuvant therapies can reduce the metastatic risk, which implies that some of these patients harbour isolated tumour cells or micrometastases (minimal residual disease, MRD) that are undetectable by radiological imaging and conventional histopathology but can still be the cause of tumour recurrence. Therefore, reliable methods for diagnosing MRD would be desirable for individually tailoring therapy for these patients. Unfortunately, testing methods for MRD and interpretation of their results are not standardised and studies published on this topic are difficult to interpret due to methodological differences and small sample sizes. As of now, testing for MRD has not become relevant in clinical routine for any of the anatomic compartments lymph nodes, peritoneal lavage fluid, peripheral blood, and bone marrow in the Western hemisphere. Most reliable data on MRD in gastric cancer patients have been reported for peritoneal lavage fluid. In some centres in Japan, this test is routinely being used for making therapeutic decisions, e. g., on the use of intraperitoneal chemotherapy. MRD in resected lymph nodes will be further evaluated in the context of the sentinel lymph node concept and possibly be employed for designing individualised therapy for patients in early disease stages who are not routinely candidates for multimodal treatment. As for tumour cells in peripheral blood and in bone marrow, studies suggest that these cells are only able to form metastases in the presence of certain molecular factors. Therefore, rather than simply confirming the existence of isolated tumour cells in blood or bone marrow, future studies should concentrate on defining their molecular characteristics and the conditions required for their metastatic potential. This may gain relevance in diagnostics and prognostic evaluation of individual patients as well as in the development of targeted therapies directly interfering with the metastatic process.
机译:尽管最近在胃癌治疗方面取得了进展,但该疾病的预后在晚期仍很差。在许多情况下,即使没有任何残留肿瘤的经过治疗的患者也会发生异时转移。与其他实体瘤一样,辅助治疗可以降低转移风险,这意味着其中一些患者具有孤立的肿瘤细胞或微小转移灶(最小残留疾病,MRD),这些影像学检查或放射线成像和常规组织病理学检测不到,但仍可能是肿瘤复发。因此,对于这些患者的个体定制疗法,将需要可靠的诊断MRD的方法。不幸的是,MRD的测试方法及其结果的解释尚未标准化,并且由于方法论上的差异和样本量较小,因此难以解释有关该主题的研究。到目前为止,在西半球的任何解剖室,淋巴结,腹腔灌洗液,外周血和骨髓中,MRD的检测在临床上均已不相关。对于胃癌患者的腹膜灌洗液,已经报道了最可靠的MRD数据。在日本的某些中心,该测试通常用于制定治疗决策,例如g。关于腹膜内化疗的使用。在前哨淋巴结概念的背景下,将进一步评估切除的淋巴结中的MRD,并可能用于为疾病早期的患者设计个性化治疗,这些患者通常不适合多模式治疗。至于外周血和骨髓中的肿瘤细胞,研究表明这些细胞仅在存在某些分子因子的情况下才能形成转移灶。因此,未来的研究不仅要简单地确定血液或骨髓中是否存在分离的肿瘤细胞,还应着眼于确定其分子特征和转移潜能所需的条件。这可能与单个患者的诊断和预后评估以及直接干扰转移过程的靶向疗法的开发有关。

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