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帕唑帕尼治疗晚期肾细胞癌患者的前瞻性观察研究(PRINCIPAL 研究)。

Prospective Observational Study of Pazopanib in Patients with Advanced Renal Cell Carcinoma (PRINCIPAL Study).

机构信息

Medical University of Vienna, Vienna, Austria

National and Kapodistrian University of Athens Alexandra Hospital, Athens, Greece.

出版信息

Oncologist. 2019 Apr;24(4):491-497. doi: 10.1634/theoncologist.2018-0787. Epub 2019 Mar 13.

Abstract

BACKGROUND

Real-world data are essential to accurately assessing efficacy and toxicity of approved agents in everyday practice. PRINCIPAL, a prospective, observational study, was designed to confirm the real-world safety and efficacy of pazopanib in patients with advanced renal cell carcinoma (RCC).

SUBJECTS, MATERIALS, AND METHODS: Patients with clear cell advanced/metastatic RCC and a clinical decision to initiate pazopanib treatment within 30 days of enrollment were eligible. Primary objectives included progression-free survival (PFS), overall survival (OS), objective response rate (ORR), relative dose intensity (RDI) and its effect on treatment outcomes, change in health-related quality of life (HRQoL), and safety. We also compared characteristics and outcomes of clinical-trial-eligible (CTE) patients, defined using COMPARZ trial eligibility criteria, with those of non-clinical-trial-eligible (NCTE) patients. Secondary study objectives were to evaluate clinical efficacy, safety, and RDI in patient subgroups.

RESULTS

Six hundred fifty-seven patients were enrolled and received ≥1 dose of pazopanib. Median PFS and OS were 10.3 months (95% confidence interval [CI], 9.2-12.0) and 29.9 months (95% CI, 24.7 to not reached), respectively, and the ORR was 30.3%. HRQoL showed no or little deterioration over time. Treatment-related serious adverse events (AEs) and AEs of special interest occurred in 64 (9.7%), and 399 (60.7%) patients, respectively. More patients were classified NCTE than CTE (85.2% vs. 14.8%). Efficacy of pazopanib was similar between the two groups.

CONCLUSION

PRINCIPAL confirms the efficacy and safety of pazopanib in patients with advanced/metastatic RCC in a real-world clinical setting.

IMPLICATIONS FOR PRACTICE

PRINCIPAL is the largest ( = 657) prospective, observational study of pazopanib in patients with advanced/metastatic renal cell carcinoma, to the authors' knowledge. Consistent with clinical trial results that often contain specific patient types, the PRINCIPAL study demonstrated that the effectiveness and safety of pazopanib is similarly safe and effective in patients with advanced kidney cancer in a real-world clinical setting. The PRINCIPAL study showed that patients with advanced kidney cancer who are treated with first-line pazopanib generally do not show disease progression for approximately 10 months and generally survive for nearly 30 months.

摘要

背景

真实世界的数据对于准确评估已批准药物在日常实践中的疗效和毒性至关重要。PRINCIPAL 是一项前瞻性、观察性研究,旨在确认帕唑帕尼在晚期肾细胞癌(RCC)患者中的真实世界安全性和疗效。

受试者、材料和方法:符合条件的患者为患有透明细胞晚期/转移性 RCC,且在入组后 30 天内有临床决策开始使用帕唑帕尼治疗。主要目标包括无进展生存期(PFS)、总生存期(OS)、客观缓解率(ORR)、相对剂量强度(RDI)及其对治疗结果的影响、健康相关生活质量(HRQoL)的变化以及安全性。我们还比较了符合 COMPARZ 试验入选标准的临床试验合格(CTE)患者与不符合临床试验合格(NCTE)患者的特征和结局。次要研究目的是评估患者亚组的临床疗效、安全性和 RDI。

结果

657 名患者入组并接受了至少 1 剂帕唑帕尼。中位 PFS 和 OS 分别为 10.3 个月(95%置信区间 [CI],9.2-12.0)和 29.9 个月(95%CI,24.7 至未达到),ORR 为 30.3%。HRQoL 随时间无或很少恶化。64 例(9.7%)和 399 例(60.7%)患者分别发生治疗相关严重不良事件(AE)和特别关注的 AE。与 CTE 相比,更多患者被归类为 NCTE(85.2%比 14.8%)。帕唑帕尼的疗效在两组间相似。

结论

PRINCIPAL 在真实临床环境中证实了帕唑帕尼在晚期/转移性 RCC 患者中的疗效和安全性。

实践意义

据作者所知,PRINCIPAL 是迄今为止针对晚期/转移性肾细胞癌患者进行的最大规模( = 657)前瞻性、观察性帕唑帕尼研究。与经常包含特定患者类型的临床试验结果一致,PRINCIPAL 研究表明,在真实世界的临床环境中,帕唑帕尼在晚期肾癌患者中的有效性和安全性同样安全有效。PRINCIPAL 研究表明,接受一线帕唑帕尼治疗的晚期肾癌患者通常约 10 个月内不会出现疾病进展,并且通常生存近 30 个月。

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