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阿昔替尼在疾病进展时剂量递增作为转移性肾细胞癌治疗策略。

Dose escalation of axitinib on disease progression as a strategy in the treatment of metastatic renal cell carcinoma.

作者信息

Doherty Gary Joseph, Lynskey Deirdre, Matakidou Athena, Fife Kate, Eisen Tim

机构信息

Department of Oncology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.

出版信息

ESMO Open. 2018 Nov 5;3(7):e000445. doi: 10.1136/esmoopen-2018-000445. eCollection 2018.

Abstract

INTRODUCTION

The AXIS trial established axitinib as a standard of care treatment for patients with metastatic renal cell carcinoma (mRCC) after failure of a prior tyrosine kinase inhibitor. Axitinib dosing begins at 5  mg twice daily, with escalation of doses to 7  and 10  mg after consecutive 2-week intervals if tolerated (as per the drug label). Given clinical concerns about drug-related toxicity, we have used a pragmatic strategy where dose escalations were made only after disease progression or where rapid responses were clinically required.

METHODS

We performed a retrospective review of electronic health records and radiology of all patients with mRCC treated with axitinib for >2 weeks at Addenbrooke's Hospital, Cambridge, UK, over a 37 -month period to determine the clinical and radiological effects of dose escalations made according to the above strategy.

RESULTS

42 patients fitting these criteria were identified, 29 having ≥1  dose escalation event (DEE). 60 DEEs were identified (median of two per patient), and the objective radiological consequences of 53 DEEs could be evaluated. The disease control rate (partial response or stable disease) after the first DEE instituted for disease progression was similar to that after the second DEE (68.8% vs 70%). 56.6 % of all DEEs and 63.6 % of DEEs made as a result of disease progression resulted in disease control. The median OS from the commencement of axitinib for all dose-escalated patients was 19.9 months, and 16.5 months for the entire cohort. The mean dose (for all patients) at 90 days after starting axitinib was 5.92  mg.

CONCLUSION

These data suggest that dose escalation of axitinib after disease progression may be an effective dosing strategy for patients with mRCC, and this may be a preferred option in patients in whom there are particular concerns about drug-related toxicity, quality of life optimisation or healthcare-associated costs.

摘要

引言

AXIS试验确立了阿昔替尼作为先前酪氨酸激酶抑制剂治疗失败后的转移性肾细胞癌(mRCC)患者的标准治疗方案。阿昔替尼的给药起始剂量为每日两次,每次5毫克,如果耐受(根据药品标签),连续2周后剂量可增至7毫克和10毫克。鉴于对药物相关毒性的临床关注,我们采用了一种务实的策略,即仅在疾病进展后或临床需要快速反应时才进行剂量递增。

方法

我们对英国剑桥阿登布鲁克医院在37个月期间接受阿昔替尼治疗超过2周的所有mRCC患者的电子健康记录和放射学资料进行了回顾性分析,以确定根据上述策略进行剂量递增的临床和放射学效果。

结果

确定了42例符合这些标准的患者,其中29例发生≥1次剂量递增事件(DEE)。共确定了60次DEE(每位患者中位数为2次),其中53次DEE的客观放射学后果可进行评估。因疾病进展而进行的首次DEE后的疾病控制率(部分缓解或病情稳定)与第二次DEE后的相似(68.8%对70%)。所有DEE中有56.6%以及因疾病进展而进行的DEE中有63.6%导致疾病得到控制。所有剂量递增患者从开始使用阿昔替尼起的中位总生存期为19.9个月,整个队列的中位总生存期为16.5个月。开始使用阿昔替尼90天后的平均剂量(所有患者)为5.92毫克。

结论

这些数据表明,疾病进展后阿昔替尼剂量递增可能是mRCC患者的一种有效给药策略,对于特别关注药物相关毒性、生活质量优化或医疗相关成本的患者而言,这可能是一个首选方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52cf/6241974/189f74e6e079/esmoopen-2018-000445f01.jpg

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