Stahlecker J, Gauger A, Bosserhoff A, Büttner R, Ring J, Hein R
Klinik und Poliklinik für Dermatologie und Allergologie am Biederstein, Technische Universität München, Germany.
Anticancer Res. 2000 Nov-Dec;20(6D):5041-4.
Reports published in 1996 concerning the protein MIA proposed it as a useful tumor marker for patients suffering from malignant melanoma. Therefore we systematically started to measure MIA levels in patients with malignant melanoma. It was and still is questionable whether MIA in the serum of melanoma patients is a reliable tumor marker in terms of course of disease, therapy-monitoring and prognostic value. Previous studies have already confirmed the specifity of MIA as a tumor marker for malignant melanoma.
Using an ELISA- System, we examined over 830 blood samples of 326 melanoma patients. The cut-off was determined at 9.8 ng/ml.
5.6% (n = 17) of melanoma patients at stage I/II (n = 302) showed increased MIA levels, whereas at stage III/IV (n = 5/n = 19) high levels were found in 60.0% and 89.5% respectively. Patients at stage III/IV with MIA levels below the cut-off turned out to be the ones after metastatic surgery, irradiation or chemotherapy. None of these patients developed further metastases during follow-up, just as patients at stage I/II without increased MIA levels. After a distinct rise of MIA levels, metastases could be detected at the same time or shortly after. On the other hand we saw decreasing levels after or during therapy.
Our data showed that MIA is a suitable serum marker to detect metastases and to monitor course and therapy of disease. The prognostic value (increased MIA levels at stage I/II), however, requires further investigation.
1996年发表的有关MIA蛋白的报告提出,它是恶性黑色素瘤患者有用的肿瘤标志物。因此,我们系统地开始检测恶性黑色素瘤患者的MIA水平。就疾病进程、治疗监测和预后价值而言,黑色素瘤患者血清中的MIA是否为可靠的肿瘤标志物,过去存在疑问,现在依然如此。先前的研究已经证实MIA作为恶性黑色素瘤肿瘤标志物的特异性。
我们使用酶联免疫吸附测定(ELISA)系统检测了326例黑色素瘤患者的830多份血样。临界值确定为9.8 ng/ml。
I/II期(n = 302)的黑色素瘤患者中有5.6%(n = 17)MIA水平升高,而在III/IV期(n = 5/n = 19),分别有60.0%和89.5%的患者MIA水平升高。III/IV期MIA水平低于临界值的患者是那些接受过转移灶手术、放疗或化疗的患者。在随访期间,这些患者均未发生进一步转移,I/II期MIA水平未升高的患者也是如此。MIA水平明显升高后,可同时或不久后检测到转移灶。另一方面,我们在治疗后或治疗期间看到MIA水平下降。
我们的数据表明,MIA是检测转移灶以及监测疾病进程和治疗的合适血清标志物。然而,其预后价值(I/II期MIA水平升高)还需要进一步研究。