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唑来膦酸治疗 IIIA/B 期 NSCLC 患者的随机 III 期研究结果。

Zoledronic acid in patients with stage IIIA/B NSCLC: results of a randomized, phase III study.

机构信息

Department of Clinical and Biological Sciences, University of Turin, Torino, Italy.

Department of Oncology, Hygeia Hospital, Athens, Greece.

出版信息

Ann Oncol. 2012 Aug;23(8):2082-2087. doi: 10.1093/annonc/mds128. Epub 2012 Jun 22.

Abstract

BACKGROUND

Bone metastases are common in patients with advanced non-small-cell lung cancer (NSCLC) and can have devastating consequences. Preventing or delaying bone metastases may improve outcomes.

PATIENTS AND METHODS

This study evaluated whether zoledronic acid (ZOL) delayed disease progression or recurrence in patients with controlled stage IIIA/B NSCLC after first-line therapy. Patients received vitamin D and calcium supplementation and were randomized to i.v. ZOL (every 3-4 weeks) or no treatment (control). The primary end point was progression-free survival (PFS).

RESULTS

No significant intergroup differences were observed in PFS or overall survival (OS). Median PFS was 9.0 months with ZOL versus 11.3 months for control. Fifteen ZOL-treated (6.6%) and 19 control patients (9.0%) developed bone metastases. Estimated 1-year OS was 81.8% for each group. ZOL safety profile was consistent with previous clinical data, but with higher discontinuations versus control. Fifteen ZOL-treated (6.6%) and five control patients (2.3%) had renal adverse events. Two cases of osteonecrosis of the jaw were reported.

CONCLUSIONS

ZOL did not significantly affect PFS or OS in stage IIIA/B NSCLC patients with controlled disease, with a trend toward worsening PFS in the longer-term follow-up. Few patients experienced bone metastases, possibly limiting the potential ZOL impact on disease course.

摘要

背景

骨转移在晚期非小细胞肺癌(NSCLC)患者中很常见,可能会产生毁灭性的后果。预防或延迟骨转移可能会改善预后。

患者和方法

本研究评估唑来膦酸(ZOL)是否会延迟一线治疗后控制的 IIIA/B 期 NSCLC 患者的疾病进展或复发。患者接受维生素 D 和钙补充,并随机接受静脉内 ZOL(每 3-4 周)或不治疗(对照组)。主要终点是无进展生存期(PFS)。

结果

在 PFS 或总生存期(OS)方面,两组之间没有观察到显著的组间差异。ZOL 组的中位 PFS 为 9.0 个月,对照组为 11.3 个月。15 名 ZOL 治疗(6.6%)和 19 名对照组患者(9.0%)发生骨转移。两组估计的 1 年 OS 分别为 81.8%。ZOL 的安全性特征与之前的临床数据一致,但与对照组相比,停药率更高。15 名 ZOL 治疗(6.6%)和 5 名对照组患者(2.3%)出现肾脏不良事件。报告了两例下颌骨坏死病例。

结论

ZOL 并未显著影响疾病得到控制的 IIIA/B 期 NSCLC 患者的 PFS 或 OS,在更长时间的随访中 PFS 有恶化的趋势。少数患者发生骨转移,这可能限制了 ZOL 对疾病进程的潜在影响。

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