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半胱氨酰多巴在播散性恶性黑色素瘤随访中的价值。

The value of cysteinyldopa in the follow-up of disseminated malignant melanoma.

作者信息

Kärnell R, Kågedal B, Lindholm C, Nilsson B, Arstrand K, Ringborg U

机构信息

Department of General Oncology Radiumhemmet, Karolinska Hospital, Stockholm, Sweden.

出版信息

Melanoma Res. 2000 Aug;10(4):363-9. doi: 10.1097/00008390-200008000-00008.

Abstract

In a series of 92 patients with malignant melanoma, clinical stage III or IV, both 5-S-cysteinyldopa (5SCD) and 6-hydroxy-5-methoxyindole-2-carboxylic acid (6H5MI2C) were measured in urine during chemotherapy. A total of 434 urine specimens were analysed. The sensitivity of 5SCD for the detection of stage III-IV melanoma was 83%, while the corresponding sensitivity of 6H5MI2C was 52%. Fifty per cent of patients with one metastatic site had increased 5SCD excretion, while all patients with four or more metastatic sites had increased excretion. A significant correlation was found between 5SCD decrease and clinical regression (P<0.001) and between 5SCD increase and clinical progression (P<0.001). Corresponding correlations were not found for 6H5MI2C. Increments in 5SCD excretion (median 269 micromol/mol creatinine) were seen for 83% of the occasions when clinical progression was recorded, and decrements in 5SCD excretion (median 145 micromol/mol creatinine) were seen for 85% of the occasions when clinical regression was seen. During clinical 'stable disease' increases in 5SCD excretion were seen in 59% and decreases in 41%. The median value of 5SCD changes for stable disease was 7.0 micromol/mol creatinine, indicating a chemical marker stability in many cases. We recommend the use of 5SCD in urine as a valuable, reliable and simple biochemical marker to use in the clinical follow-up of melanoma patients with advanced disease.

摘要

在一组92例临床分期为III期或IV期的恶性黑色素瘤患者中,在化疗期间检测了尿中的5-S-胱氨酸多巴(5SCD)和6-羟基-5-甲氧基吲哚-2-羧酸(6H5MI2C)。共分析了434份尿液标本。5SCD检测III-IV期黑色素瘤的敏感性为83%,而6H5MI2C的相应敏感性为52%。有一个转移部位的患者中有50%的5SCD排泄增加,而所有有四个或更多转移部位的患者排泄均增加。发现5SCD降低与临床缓解之间存在显著相关性(P<0.001),5SCD升高与临床进展之间也存在显著相关性(P<0.001)。未发现6H5MI2C有相应的相关性。当记录到临床进展时,83%的情况下可见5SCD排泄增加(中位数为269微摩尔/摩尔肌酐),当出现临床缓解时,85%的情况下可见5SCD排泄减少(中位数为145微摩尔/摩尔肌酐)。在临床“疾病稳定”期间,59%的患者5SCD排泄增加,41%的患者排泄减少。疾病稳定时5SCD变化的中位数为7.0微摩尔/摩尔肌酐,表明在许多情况下化学标志物稳定。我们建议将尿中的5SCD用作一种有价值、可靠且简单的生化标志物,用于晚期黑色素瘤患者的临床随访。

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