Radiation Oncology Department, Hospital Central de la Defensa Gómez Ulla, Madrid, Spain.
Clin Transl Oncol. 2010 Aug;12(8):568-73. doi: 10.1007/s12094-010-0555-z.
We evaluated serum C-telopeptides (CTX) to see whether they may be useful as predictive markers for disease progression in cancer patients with bone metastases who are being treated with zoledronic acid (ZA).
This was a prospective, nonrandomised study in which 26 patients with solid tumours and confirmed bone metastases were treated with ZA (4 mg every 3-4 weeks) for 24 months or until a skeletal-related event (SRE) was observed. Serum CTX levels were determined at baseline and 6, 12, 18 and 24 months after study initiation. SRE were evaluated using bone scintigraphy.
Study participants had prostate (50%), breast (31%), lung (11%) or bladder (8%) tumours. Mean age was 69 (range 52-84) years, and 65% men. At baseline, overall mean CTX levels were 562.47 ± 305.17 pg/dl. Patients who showed disease progression during the study period showed significantly higher CTX levels at baseline and after 18 months of ZA treatment than patients who did not progress (p = 0.040 and p = 0.006, respectively). Patients with ≥ 5 bone metastases at diagnosis had significantly higher CTX levels after 18 months of ZA treatment than patients with < 5 bone metastasis (p = 0.001). Similarly, at 12 and 18 months, patients without SRE had significantly lower CTX levels than patients in whom a SRE was observed (p = 0.005 and p = 0.001, respectively).
Changes in serum CTX levels seem to predict the potential for tumour control and the likelihood of developing an SRE in a sample of patients with solid tumours and bone metastases treated with ZA.
我们评估了血清 C 端肽(CTX),以观察其是否可作为接受唑来膦酸(ZA)治疗的伴有骨转移的癌症患者疾病进展的预测标志物。
这是一项前瞻性、非随机研究,共纳入 26 例经组织学证实的伴有骨转移的实体瘤患者,接受 ZA(每 3-4 周 4mg)治疗 24 个月或直至出现骨骼相关事件(SRE)。在研究开始时及 6、12、18 和 24 个月时测定血清 CTX 水平。通过骨闪烁显像评估 SRE。
研究参与者的肿瘤分别来自前列腺(50%)、乳腺(31%)、肺(11%)或膀胱(8%)。平均年龄为 69(52-84)岁,65%为男性。基线时,总体平均 CTX 水平为 562.47±305.17pg/dl。研究期间疾病进展的患者,其基线和 ZA 治疗 18 个月后的 CTX 水平显著高于未进展的患者(p=0.040 和 p=0.006)。诊断时伴有≥5 处骨转移的患者,ZA 治疗 18 个月后的 CTX 水平显著高于伴有<5 处骨转移的患者(p=0.001)。同样,在 12 和 18 个月时,无 SRE 的患者的 CTX 水平显著低于发生 SRE 的患者(p=0.005 和 p=0.001)。
血清 CTX 水平的变化似乎可预测接受 ZA 治疗的伴有骨转移的实体瘤患者的肿瘤控制潜力和发生 SRE 的可能性。