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舒尼替尼治疗转移性肾细胞癌(mRCC)患者的经验:来自西班牙 3 项观察性前瞻性研究的汇总分析。

Experience with Sunitinib in metastatic renal cell carcinoma (mRCC) patients: pooled analysis from 3 Spanish observational prospective studies.

机构信息

a Hospital Universitario 12 de Octubre , Madrid , Spain.

b Medical Oncology , Hospital de la Santa Creu i Sant Pau , Barcelona , Spain.

出版信息

Expert Opin Drug Saf. 2018 Jun;17(6):573-579. doi: 10.1080/14740338.2017.1330410. Epub 2017 Aug 28.

Abstract

BACKGROUND

A pivotal, randomized, phase III trial demonstrated a statistically significant superiority of sunitinib over interferon-α in metastatic renal cell carcinoma (mRCC) patients.

OBJECTIVE

To evaluate the effectiveness and safety of sunitinib in patients with advanced or mRCC in routine clinical practice.

METHODS

Retrospective pooled analysis of clinical data from three observational and prospective studies carried out between 2007 and 2011 in 33 Spanish hospitals. Tumor response, Progression-free survival (PFS) and overall survival (OS), and main sunitinib-related toxicities were registered.

RESULTS

224 patients were analyzed. Median PFS 10.6 months (95% CI: 9.02-12.25), median OS 21.9 months (95% CI: 17.2-26.6). Objective response rate (ORR) 43.8% (95% CI: 36.8-50.7). Median time to PR was 3.8 months (95% CI: 3.86-5.99) and to CR 8.2 months (95% CI: 4.75-9.77). The most common ≥ grade-3 AEs were asthenia/fatigue (18.7%), hand-foot syndrome (6.2%), hypertension (5.8%) and neutropenia (4.8%). Hand-foot syndrome, diarrhea and mucositis were confirmed as independent predictors for PFS and/or OS in a multivariate analysis (p < 0.05) Conclusions: Outcomes with sunitinib in daily clinical practice resemble those obtained in clinical trials. Long-term benefit with sunitinib is possible in advanced RCC patients but the appropriate management of toxicities is mandatory to enable patients to remain on treatment.

摘要

背景

一项关键性、随机、III 期试验表明舒尼替尼在转移性肾细胞癌(mRCC)患者中的疗效明显优于干扰素-α。

目的

评估舒尼替尼在常规临床实践中治疗晚期或 mRCC 患者的疗效和安全性。

方法

回顾性分析了 2007 年至 2011 年间在西班牙 33 家医院进行的三项观察性和前瞻性研究的临床数据。记录肿瘤反应、无进展生存期(PFS)和总生存期(OS)以及主要的舒尼替尼相关毒性。

结果

分析了 224 例患者。中位 PFS 为 10.6 个月(95%CI:9.02-12.25),中位 OS 为 21.9 个月(95%CI:17.2-26.6)。客观缓解率(ORR)为 43.8%(95%CI:36.8-50.7)。PR 的中位时间为 3.8 个月(95%CI:3.86-5.99),CR 为 8.2 个月(95%CI:4.75-9.77)。最常见的≥3 级不良事件为乏力/疲劳(18.7%)、手足综合征(6.2%)、高血压(5.8%)和中性粒细胞减少(4.8%)。在多变量分析中,手足综合征、腹泻和黏膜炎被确认为 PFS 和/或 OS 的独立预测因素(p<0.05)。

结论

舒尼替尼在日常临床实践中的疗效与临床试验相似。舒尼替尼对晚期 RCC 患者可能具有长期获益,但必须对毒性进行适当管理,以使患者能够继续接受治疗。

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