Seibel M J, Koeller M, Van der Velden B, Diel I
Dept. of Endocrinology & Metabolism, Concord Hospital Medical Centre, University of Sydney, Australia.
Clin Lab. 2002;48(11-12):583-8.
Markers of bone turnover are often elevated in patients with prevalent bone metastases (BM). To test whether bone markers may be used as early indicators of developing BM, we prospectively studied 113 women with primary breast cancer. At the time of study inclusion, none of the women had BM, skeletal disease or was on bone active drugs. During follow-up (8-52, median 30 mo.), pt. were seen every 3 mo. and blood/urine specimens were obtained. Eleven patients developed BM (BM+) and each of them was matched to 4 women remaining free of BM (BM-). Markers were serum (s) calcium, sTAP, sBAP, sOC, sPICP, sNTX, sCTX and urinary (u) PYD, uDPD, uNTX, uCTX. All analyses were done in single batches after study end. At any given point in time, marker levels in the BM+ group did not differ from those in the BM- group. Levels at baseline did not predict later BM (OR 0.14-1.01, all ns). 93% of all changes in bone markers were below the least significant change, as defined in an independent group of similar patients. The remaining 7% of values could not be associated in a consistent pattern with the occurrence of BM. We conclude that in patients with primary breast cancer, biochemical markers of bone turnover can not be used to predict or diagnose incident BM. This lack in diagnostic validity is mainly attributable to the high overall and long-term variability of the currently used bone markers.
在患有骨转移(BM)的患者中,骨转换标志物通常会升高。为了测试骨标志物是否可作为发生骨转移的早期指标,我们对113例原发性乳腺癌女性进行了前瞻性研究。在纳入研究时,这些女性均无骨转移、骨骼疾病,也未使用骨活性药物。在随访期间(8 - 52个月,中位时间30个月),患者每3个月就诊一次,并采集血液/尿液样本。11例患者发生了骨转移(BM+),每例患者与4例未发生骨转移(BM-)的女性进行匹配。标志物包括血清(s)钙、sTAP、sBAP、sOC、sPICP、sNTX、sCTX以及尿(u)PYD、uDPD、uNTX、uCTX。所有分析均在研究结束后成批进行。在任何给定时间点,BM+组的标志物水平与BM-组的标志物水平无差异。基线水平无法预测后期是否发生骨转移(OR为0.14 - 1.91,均无统计学意义)。在一组独立的类似患者中,93%的骨标志物变化低于最小显著变化。其余7%的值与骨转移的发生无一致的关联模式。我们得出结论,在原发性乳腺癌患者中,骨转换的生化标志物不能用于预测或诊断新发骨转移。这种诊断有效性的缺乏主要归因于目前使用的骨标志物总体和长期的高变异性。