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唑来膦酸联合顺铂-多西他赛作为晚期非小细胞肺癌伴骨转移一线治疗的可行性研究。

Feasibility study of zoledronic acid plus cisplatin-docetaxel as first-line treatment for advanced non-small cell lung cancer with bone metastases.

机构信息

Division of Thoracic Oncology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.

出版信息

Anticancer Res. 2012 Sep;32(9):4131-5.

Abstract

BACKGROUND

This study evaluated the safety and efficacy of combined zoledronic acid, cisplatin and docetaxel in patients with non-small cell lung cancer (NSCLC) with bone metastases.

PATIENTS AND METHODS

Cisplatin 80 mg/m(2) and docetaxel 60 mg/m(2) with zoledronic acid 4 mg were given intravenously on day 1 every 3-4 weeks. The primary endpoint was feasibility of concomitant administration of zoledronic acid and cisplatin.

RESULTS

Thirty-five chemonaïve patients were enrolled. The median number of treatment cycles was four, and two or more cycles were administered in 29 (83%) patients without severe toxicity. No grade 3 or 4 renal toxicity was observed. The objective response rate was 29% and the 1-year survival rate was 37%. The pain score improved in 77% of the patients after six weeks.

CONCLUSION

The combination of zoledronic acid, cisplatin and docetaxel is well-tolerated with acceptable renal toxicity, and has modest activity as a first-line treatment of NSCLC patients with bone metastases.

摘要

背景

本研究评估了唑来膦酸、顺铂和多西他赛联合治疗非小细胞肺癌(NSCLC)伴骨转移患者的安全性和有效性。

患者和方法

顺铂 80mg/m² 和多西他赛 60mg/m² 联合唑来膦酸 4mg 静脉滴注,每 3-4 周一次。主要终点是唑来膦酸和顺铂联合给药的可行性。

结果

35 例化疗初治患者入组。中位治疗周期数为 4 个,29 例(83%)患者无严重毒性,接受了 2 个或更多周期的治疗。未观察到 3 级或 4 级肾毒性。客观缓解率为 29%,1 年生存率为 37%。6 周后,77%的患者疼痛评分改善。

结论

唑来膦酸、顺铂和多西他赛联合治疗具有可接受的肾毒性,耐受性良好,作为 NSCLC 伴骨转移患者的一线治疗具有一定的活性。

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