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Multicenter study of zoledronic acid administration in non-small-cell lung cancer patients with bone metastasis: Thoracic Oncology Research Group (TORG) 1017

机译:唑来膦酸在非小细胞肺癌骨转移患者中的多中心研究:胸部肿瘤研究组(TORG)1017

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摘要

Skeletal-related events (SREs) may occur at the time of first diagnosis in 20–30% of lung cancer patients with bone metastases. Several clinical trials have shown that zoledronic acid (ZA) is effective for decreasing SREs. The main objective of the present study was to discuss clinical data of ZA and compare the frequency of SREs with previous reports. All patients with non-small-cell lung cancer (NSCLC) with metastatic bone disease who were administered ZA at least twice between January 2008 and December 2009 were eligible for inclusion in the study. In total, 198 consecutive patients were identified. The median duration of ZA administration was 106 days [95% confidence interval (CI), 92–133 days], and the median number of ZA administrations was 4 (range, 2–41). The median time to first SRE in patients who experienced SRE following ZA treatment was 202 days (95% CI, 156–264 days). Among the 78 patients who had already experienced SRE prior to ZA treatment, 35 (45%) experienced SRE subsequently after starting ZA treatment. On the other hand, among the 120 patients without a history of SRE before starting ZA treatment, 42 (35%) experienced SRE after the start of ZA administration (P=0.16). No osteonecrosis of the jaw (ONJ) was reported in any of the patients. The present study revealed that ZA had a certain level of efficacy regardless of the presence or absence of prior SREs. However, the duration of ZA therapy was short in this study; further accumulation of data on the long-term prognosis and incidence rates of ONJ and other late complications of ZA therapy seems to be particularly important.
机译:在首次诊断时,有20-30%的骨转移肺癌患者可能发生骨骼相关事件(SRE)。多项临床试验表明,唑来膦酸(ZA)可有效降低SRE。本研究的主要目的是讨论ZA的临床数据,并将SRE的发生频率与以前的报道进行比较。所有患有转移性骨疾病的非小细胞肺癌(NSCLC)患者在2008年1月至2009年12月之间至少接受过ZA两次,均符合纳入研究的条件。总共确定了198位连续患者。 ZA给药的中位时间为106天[95%置信区间(CI),92-133天],ZA给药的中位数为4(范围2–41)。 ZA治疗后经历SRE的患者中首次SRE的中位时间为202天(95%CI,156–264天)。在ZA治疗之前已经经历过SRE的78例患者中,有35例(45%)在开始ZA治疗之后随后经历了SRE。另一方面,在开始ZA治疗前无SRE病史的120例患者中,有42例(35%)在开始ZA治疗后经历过SRE(P = 0.16)。在所有患者中均未报告颌骨骨坏死(ONJ)。本研究表明,无论是否存在先前的SRE,ZA都具有一定水平的疗效。然而,ZA研究的持续时间很短。进一步收集ONJ的长期预后和发生率以及ZA治疗的其他晚期并发症的数据似乎特别重要。

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