Pectasides Dimitrios, Nikolaou Maria, Farmakis Dimitrios, Kanakis Ioannis, Gaglia Asimina, Kountourakis Pantelis, Karamanos Nikolaos K, Economopoulos Theofanis, Raptis Sotirios A
Second Department of Internal Medicine-Propaedeutic, Athens University Medical School, Attikon University Hospital, Athens, Greece.
Anticancer Res. 2005 Mar-Apr;25(2B):1457-63.
Bisphosphonates have an established role in the treatment of bone metastases from a variety of solid tumours. The objective response to anti-resorptive treatment cannot be evaluated by imaging techniques. A number of bone remodelling markers have been associated with bone metastases status; among them, urine and serum levels of N-terminal telopeptide of collagen type I (NTx) seem to have the best diagnostic accuracy. However, serum NTx has not yet been properly evaluated.
Seventy-one consecutive patients with newly diagnosed skeletal metastases were enrolled in this prospective study. All of them were treated with zoledronic acid at 4 mg, every 3 or 4 weeks. Serum NTx and bone-isoform of alkaline phosphatase (BAP) were measured by enzyme-linked immunosorbent assays at baseline and every 2 months thereafter.
At baseline, serum NTx and BAP levels were significantly higher in patients with blastic than lytic bone lesions and in those with multiple rather than few bone site involvement. Forty-seven patients were followed for a median period of 139 days. Zoledronic acid resulted in a significant NTx reduction at first and second post-treatment evaluations (mean reduction of 43% at first evaluation); thereafter, mean NTx levels remained suppressed. In contrast, BAP levels did not show any significant changes. Bone disease progression resulted in a significant NTx elevation by an average of 69%. The initial response of NTx to zoledronic acid was correlated with the long-term clinical outcome of bone disease: patients with an initial NTx elevation had a significantly higher rate of bone disease progression compared to those with an initial NTx decline (66.7% versus 18.8%, p=0.001). Extraskeletal disease or bone irradiation did not influence NTx response.
Serum NTx appears to be a useful marker in monitoring patients with skeletal metastases, as it is correlated with the type and bulk of bone disease and reflects bone disease progression. It is also useful in monitoring bisphosphonate therapy, while the initial response to this therapy seems to bear a prognostic significance for bone disease outcome.
双膦酸盐在多种实体瘤骨转移的治疗中已确立了作用。抗吸收治疗的客观反应无法通过影像学技术评估。一些骨重塑标志物与骨转移状态相关;其中,I型胶原N端肽(NTx)的尿液和血清水平似乎具有最佳诊断准确性。然而,血清NTx尚未得到充分评估。
71例新诊断为骨转移的连续患者纳入了这项前瞻性研究。他们均接受每3或4周一次的4mg唑来膦酸治疗。在基线及之后每2个月通过酶联免疫吸附测定法测量血清NTx和骨碱性磷酸酶(BAP)。
基线时,成骨性骨病变患者的血清NTx和BAP水平显著高于溶骨性骨病变患者,且多骨部位受累患者高于少骨部位受累患者。47例患者的中位随访期为139天。唑来膦酸在首次和第二次治疗后评估时导致NTx显著降低(首次评估时平均降低43%);此后,平均NTx水平持续受到抑制。相比之下,BAP水平未显示任何显著变化。骨病进展导致NTx平均显著升高69%。NTx对唑来膦酸的初始反应与骨病的长期临床结果相关:初始NTx升高的患者骨病进展率显著高于初始NTx下降的患者(66.7%对18.8%,p = 0.001)。骨外疾病或骨照射不影响NTx反应。
血清NTx似乎是监测骨转移患者的有用标志物,因为它与骨病的类型和范围相关并反映骨病进展。它在监测双膦酸盐治疗中也有用,而对该治疗的初始反应似乎对骨病结果具有预后意义。