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首页> 外文期刊>The oncologist >Effect of Concomitant pHa??Elevating Medications with Pazopanib on Progressiona??Free Survival and Overall Survival in Patients with Metastatic Renal Cell Carcinoma
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Effect of Concomitant pHa??Elevating Medications with Pazopanib on Progressiona??Free Survival and Overall Survival in Patients with Metastatic Renal Cell Carcinoma

机译:伴随pHa-升高剂量的药物与帕唑帕尼联合治疗对转移性肾细胞癌患者无进展生存期和总生存期的影响

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Background. Pazopanib is an oral tyrosinea??kinase inhibitor that is approved by the U.S. Food and Drug Administration for treatment of metastatic renal cell carcinoma (mRCC). Pharmacokinetic data have shown that concomitant administration of pazopanib and esomeprazole, a proton pump inhibitor (PPI), leads to decreased area under the curve and thus decreased exposure of pazopanib by 40%. Despite the pharmacokinetic data published to date, the clinical significance and impact on patient outcomes resulting from decreased pazopanib exposure remains unknown. Materials and Methods. In this retrospective, observational, cohort study, 90 patients with mRCC who either received pazopanib in combination with a PPI or histamine 2 receptor antagonist (H2RA; concurrent PPI/H2RA group) or who did not take concurrent pHa??elevating medications (no PPI/H2RA group) were compared to determine if there was an impact on progressiona??free survival (PFS), the primary endpoint, and secondary endpoints, overall survival (OS) and safety. Results. The differences between the PFS of 9.0 months and OS of 28.0 months for the concomitant PPI/H2RA group versus 11.0 months and 30.1 months, respectively, for the no PPI/H2RA group were not statistically significant. Rates of adverse events were similar between the concomitant PPI/H2RA and no PPI/H2RA groups. Conclusion. Concomitant PPI or H2RA usage was not shown to be associated with a reduction in PFS or OS for patients receiving pazopanib for mRCC, with a similar toxicity profile in each group. Based on the results of this retrospective cohort study and the palliative nature of the treatment of patients with mRCC, clinicians should consider allowing patients to remain on concomitant pazopanib and acida??reducing therapy. Implications for Practice. Pazopanib is a preferred categorya??one firsta??line treatment for predominant clear cell metastatic renal cell carcinoma (mRCC). However, because of an aging demographic, coupled with patients with mRCC presenting with multiple comorbidities, including symptomatic dyspepsia or gastroesophageal reflux disease, patients are commonly required to take pazopanib concomitantly with a proton pump inhibitor (PPI) or a histamine 2 receptor antagonist (H2RA). Despite earlier pharmacokinetic reports suggesting that an alkaline pH may result in poorer absorption, this institutional retrospective study found no effect on clinical outcomes. These data suggest that concurrent treatment of mRCC with pazopanib and a PPI or H2RA may be safe in everyday practice.
机译:背景。帕唑帕尼是一种口服酪氨酸激酶抑制剂,已被美国食品药品监督管理局批准用于治疗转移性肾细胞癌(mRCC)。药代动力学数据显示,帕唑帕尼和质子泵抑制剂(PPI)埃索美拉唑的同时给药可导致曲线下面积减小,从而使帕唑帕尼的暴露减少40%。尽管迄今已发表了药代动力学数据,但由于帕唑帕尼暴露减少而导致的临床意义和对患者预后的影响仍然未知。材料和方法。在这项回顾性观察性队列研究中,有90例mRCC患者接受了帕唑帕尼联合PPI或组胺2受体拮抗剂(H2RA;并发PPI / H2RA组)或未同时服用pHa升高药物(无PPI)比较/ H2RA组)以确定是否对无进展生存期(PFS),主要终点和次要终点,总生存期(OS)和安全性有影响。结果。同期PPI / H2RA组的9.0个月PFS和28.0个月的OS与无PPI / H2RA组的分别为11.0个月和30.1个月之间无统计学差异。伴随的PPI / H2RA组和无PPI / H2RA组之间的不良事件发生率相似。结论。对于接受帕唑帕尼治疗mRCC的患者,未显示同时使用PPI或H2RA与PFS或OS降低相关,每组的毒性相似。根据这项回顾性队列研究的结果以及mRCC患者的姑息治疗性质,临床医生应考虑允许患者继续接受帕唑帕尼和降低酸的治疗。对实践的启示。对于主要的透明细胞转移性肾细胞癌(mRCC),帕唑帕尼是一种优选的“一线”治疗方案。然而,由于人口老龄化,加上患有多种合并症的mRCC患者,包括症状性消化不良或胃食管反流疾病,患者通常需要与质子泵抑制剂(PPI)或组胺2受体拮抗剂(H2RA)一起服用帕唑帕尼)。尽管较早的药代动力学报告表明碱性pH值可能导致吸收较差,但这项机构回顾性研究未发现对临床结果有影响。这些数据表明,帕唑帕尼和PPI或H2RA同时治疗mRCC在日常实践中可能是安全的。

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