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先前接受过酪氨酸激酶抑制剂和依维莫司治疗的转移性肾细胞癌患者,酪氨酸激酶抑制剂是否仍然有效?法国 RECORD-1 试验中 36 例患者的经验。

Are tyrosine kinase inhibitors still active in patients with metastatic renal cell carcinoma previously treated with a tyrosine kinase inhibitor and everolimus? Experience of 36 patients treated in France in the RECORD-1 Trial.

机构信息

Department of Medicine, Institut Gustave Roussy, Villejuif, France.

出版信息

Clin Genitourin Cancer. 2013 Jun;11(2):128-33. doi: 10.1016/j.clgc.2012.12.001. Epub 2013 Jan 17.

DOI:10.1016/j.clgc.2012.12.001
PMID:23332872
Abstract

BACKGROUND

Because the response to treatment is limited, patients with metastatic renal cell carcinoma (mRCC) typically receive multiple treatments. Guidelines recommend everolimus for patients previously treated with tyrosine kinase inhibitors (TKI) sunitinib or sorafenib. This study evaluated the efficacy of TKI re-treatment in patients with disease progression after a TKI-everolimus sequence.

PATIENTS AND METHODS

Data were reviewed for patients enrolled in RECORD-1 (Renal Cell Cancer Treatment With Oral RAD001 Given Daily) at French sites. Response, progression-free survival (PFS), and overall survival were evaluated in patients treated with a TKI-everolimus-TKI sequence.

RESULTS

Thirty-six patients received a TKI after everolimus: sunitinib in 17 patients, sorafenib in 15, and dovitinib (TKI258) in 4. The response rate with TKI re-treatment was 8%, and the disease-control rate (response plus stable disease) was 75%. The median PFS with each component of the TKI-everolimus-TKI sequence was 10.7 months (95% CI, 1.8-28.5 months), 8.9 months (95% CI, 1.7-34.6 months), and 8.2 months (95% CI, 5.2-11.9 months), respectively. The median overall survival from the start of everolimus was 29.1 months (95% CI 21.1 to not reached months), which suggests a benefit in using TKI in this setting.

CONCLUSIONS

Administration of a TKI-everolimus-TKI sequence may be associated with clinical benefit and should be prospectively investigated.

摘要

背景

由于治疗反应有限,转移性肾细胞癌(mRCC)患者通常需要接受多种治疗。指南建议对先前接受过酪氨酸激酶抑制剂(TKI)舒尼替尼或索拉非尼治疗的患者使用依维莫司。本研究评估了在 TKI-依维莫司序贯治疗后疾病进展的患者中重新使用 TKI 的疗效。

患者和方法

对法国站点入组 RECORD-1(每日口服 RAD001 治疗肾细胞癌)的患者数据进行了回顾。对接受 TKI-依维莫司-TKI 序贯治疗的患者进行了反应、无进展生存期(PFS)和总生存期评估。

结果

36 例患者在依维莫司后接受了 TKI 治疗:17 例患者接受舒尼替尼治疗,15 例患者接受索拉非尼治疗,4 例患者接受多韦替尼(TKI258)治疗。TKI 重新治疗的反应率为 8%,疾病控制率(反应加稳定疾病)为 75%。TKI-依维莫司-TKI 序贯治疗的每个组成部分的中位 PFS 分别为 10.7 个月(95%CI,1.8-28.5 个月)、8.9 个月(95%CI,1.7-34.6 个月)和 8.2 个月(95%CI,5.2-11.9 个月)。从依维莫司开始的中位总生存期为 29.1 个月(95%CI 21.1-未达到),这表明在这种情况下使用 TKI 具有获益。

结论

TKI-依维莫司-TKI 序贯治疗可能与临床获益相关,应进行前瞻性研究。

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