U.O. Multidisciplinare di Patologia Mammaria, U.S Terapia Molecolare e Farmacogenomica, A.O. Istituti Ospitalieri di Cremona, Viale Concordia 1, 26100, Cremona, Italy.
Breast Cancer Res Treat. 2014 Feb;144(1):113-21. doi: 10.1007/s10549-014-2840-y. Epub 2014 Jan 28.
The study investigated the anti-tumour effect of zoledronic acid (ZA) administered alone in a biological window therapy in naïve bone-only metastatic and locally advanced breast cancer (LABC) patients. 33 patients with LABC (Group 1) and 20 patients with a first diagnosis of bone metastasis only (Group 2) received 4 mg single dose of ZA, 14 days (biological window) before starting any treatment. In Group 1, Ki67, CD34, p53/bcl-2 and caspase 3 expression along with the adenosine triphosphate (ATP) levels and RNA disruption index were evaluated as markers of tumor growth in tumour specimens obtained before and after ZA administration (basal, day 14). In Group 2, the total enumeration of circulating tumour cells (CTCs), and of M30+ve CTCs along with the soluble marker of cell death (M30/M65) were carried-out as markers of tumor dissemination at baseline, at 48 h and day 14th. In Group 1, there was a significant reduction in Ki67, CD34, bcl-2 expression after 14 days ZA based-treatment (p = 0.0032; p = 0.0001, p < 0.00001 respectively). ZA showed a significant increase of RNA disruption (p < 0.0076). In Group 2, we observed a significant reduction of CTCs number after 48 h (p = 0.0012), followed by a significant rebound at 14 days (p = 0.012). The apoptotic CTCs/M30+ve and M65 levels significantly increased under treatment (p = 0.018 and p = 0.039 respectively) after drug administration when compared to the baseline. These results are the first prospective in vivo data showing the direct pure anti-tumour effect (either on the tumour cell or on CTCs) of ZA.
这项研究调查了唑来膦酸(ZA)在未经治疗的仅骨转移和局部晚期乳腺癌(LABC)患者的生物窗治疗中的单独抗肿瘤作用。33 名 LABC 患者(第 1 组)和 20 名仅首次诊断为骨转移的患者(第 2 组)在开始任何治疗前 14 天(生物窗)接受 4 毫克单剂量 ZA。在第 1 组中,Ki67、CD34、p53/bcl-2 和 caspase 3 的表达以及三磷酸腺苷(ATP)水平和 RNA 破坏指数作为 ZA 给药前后肿瘤标本中肿瘤生长的标志物进行评估(基础,第 14 天)。在第 2 组中,循环肿瘤细胞(CTC)的总计数,以及 M30+ve CTCs 以及细胞死亡的可溶性标志物(M30/M65)作为肿瘤播散的标志物在基线、48 小时和第 14 天进行。在第 1 组中,基于 14 天 ZA 治疗后 Ki67、CD34、bcl-2 表达显著降低(p=0.0032;p=0.0001,p<0.00001)。ZA 显示 RNA 破坏显著增加(p<0.0076)。在第 2 组中,我们观察到 48 小时后 CTCs 数量显著减少(p=0.0012),随后在 14 天反弹(p=0.012)。与基线相比,药物治疗后,凋亡 CTCs/M30+ve 和 M65 水平显著增加(p=0.018 和 p=0.039)。这些结果是首次在体内前瞻性数据显示 ZA 的直接纯抗肿瘤作用(无论是对肿瘤细胞还是 CTCs)。