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Detection of circulating melanoma cells in the blood of melanoma patients: a preliminary study

机译:黑色素瘤患者血液中循环黑素瘤细胞的检测:初步研究

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Significant prognostic heterogeneity exists within the substages of melanoma; therefore, novel prognostic biomarkers are needed to provide information on the risk of recurrence. Limited available data suggest prognostic significance for circulating melanoma cells (CMCs); there is a need for a sensitive, reproducible, and standardized identification technique. Using a semiautomated technology, we sought to determine whether CMCs could be identified reliably in stage I-IV melanoma patients and whether the presence of CMC correlated with known prognostic factors. CMCs were detected in the peripheral blood (7.5ml) of patients with stage I-IV melanoma (n=89) using the CellSearch system. CD146(+) cells were immunomagnetically enriched; nucleated HMW-MAA(+)/CD45(-)/CD34(-) cells were considered CMCs. One or more CMCs was detected in 45% of all patients, varying with stage of disease (stages I/II, III, and IV: 35, 44, and 86%, respectively; P=0.03, for stage I/II vs. stage IV); 55% had one CMC, 32% had two CMCs, and 13% had three or more CMCs identified. The presence of CMCs in the blood was associated with histologic subtype, particularly in patients with stage I/II disease (superficial spreading 18% vs. acral lentiginous 75%). Using a semiautomated technique, CMCs can be identified in a significant number of melanoma patients. These data support further study with longer follow-up and longitudinal/serial time points to better determine the identification rates and prognostic significance of CMCs in stage I-IV melanoma patients. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
机译:黑色素瘤的亚阶段内存在明显的预后异质性。因此,需要新的预后生物标志物来提供有关复发风险的信息。有限的可用数据提示循环黑色素瘤细胞(CMC)的预后意义;需要灵敏,可再现和标准化的识别技术。使用半自动化技术,我们试图确定在I-IV期黑色素瘤患者中是否可以可靠地鉴定CMC,以及CMC的存在是否与已知的预后因素相关。使用CellSearch系统在I-IV期黑色素瘤(n = 89)患者的外周血(7.5ml)中检测到CMC。 CD146(+)细胞免疫磁富集;有核HMW-MAA(+)/ CD45(-)/ CD34(-)细胞被视为CMC。在45%的所有患者中检测到一个或多个CMC,随疾病的阶段而变化(I / II,III和IV期:分别为35%,44%和86%;对于I / II期vs. P = 0.03。第四阶段); 55%的用户具有一个CMC,32%的用户具有两个CMC,13%的用户具有三个或更多已识别的CMC。血液中CMC的存在与组织学亚型有关,特别是在I / II期疾病患者中(表层传播为18%,而手部轻度传播为75%)。使用半自动化技术,可以在大量的黑色素瘤患者中发现CMC。这些数据为进一步的研究提供了更长的随访时间和纵向/串行时间点,以更好地确定I-IV期黑素瘤患者CMC的识别率和预后意义。版权所有(C)2015 Wolters Kluwer Health,Inc.保留所有权利。

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