临床试验专区:优化乳头状肾细胞癌护理

IF 1.1 Q4 ONCOLOGY Kidney Cancer Pub Date : 2022-10-14 DOI:10.3233/kca-229004
M. Parikh
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引用次数: 0

摘要

癌症临床试验角强调了计划或正在进行的肾8细胞癌(RCC)高影响研究。在本期中,我们重点介绍了PAPMET-2研究,这是一项重要的II期研究,评估了晚期乳头状肾细胞癌(pRCC)患者的9种治疗方法。10将来,如果你觉得你想引起人们对特定试验的关注,卡博扎替尼(NSC#761968)在晚期乳头状肾细胞癌患者中使用或不使用阿替唑珠单抗的II期随机试验研究设计:该研究纳入了患有转移性组织学证实的pRCC(1型或34 2型)的患者,这些患者具有ICI和卡博扎替尼阴性,并接受了35次一种或更少靶向药物治疗pRCC的治疗。入组后,患者随机接受36 60 mg卡博替尼口服或60 mg卡博替尼口服加atezolizumab 1200 mg静脉注射,每3 37周一次,直到疾病进展或出现不可接受的毒性。38终点:本试验的主要终点是无进展生存期(PFS)。关键的次要结果包括39例总生存率(OS)、客观反应率(ORR)以及在每个治疗组40例中观察到的定量和定性不良事件。41因为将尼沃单抗与卡博扎替尼联合的试验每天用40毫克卡博扎替尼治疗患者;在这项研究中,双臂的剂量为60mg。因此,这种剂量水平与ICI结合的耐受性将是一个重要的观察结果。这项研究的优势在于其在招募pRCC患者方面的一致性,这一点很重要,因为回顾性研究反映了基于组织学亚型的结果的异质性,毫无疑问,部分原因是对当前可用治疗的反应存在差异。
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Clinical Trials Corner: Optimizing Papillary Renal Cell Carcinoma Care
The Clinical Trials Corner of Kidney Cancer highlights planned or ongoing high-impact studies in renal cell 8 carcinoma (RCC). In this issue, we highlight the PAPMET-2 study, an important Phase II study evaluating the 9 treatment of patients with advanced papillary renal cell carcinoma (pRCC). 10 In future, if you feel that you would like to draw attention to a specific trial, A Phase II Randomized Trial of Cabozantinib (NSC#761968) With or Without Atezolizumab in Patients with Advanced Papillary Renal Cell Carcinoma Study Design: This study enrolls patients with metastatic histologically confirmed pRCC (either Type 1 or Type 34 2) with radiographically measurable disease who are ICI- and cabozantinib-na¨ıve and who have been treated 35 with one or fewer targeted therapies for pRCC. Following enrollment, patients are randomized to receive either 36 60 mg of cabozantinib orally or 60 mg of cabozantinib orally plus atezolizumab 1200 mg intravenously every 3 37 weeks, until the time of disease progression or unacceptable toxicity. 38 Endpoints: The primary endpoint of this trial is progression-free survival (PFS). Key secondary outcomes include 39 overall survival (OS), objective response rate (ORR), and quantitative & qualitative adverse events observed in 40 each treatment arm. 41 as trials combining nivolumab with cabozantinib have treated patients with 40 mg of cabozantinib daily; in this study, the dose will be 60 mg in both arms. Thus, tolerance of this dose level in combination with ICI will be an important observation. The strength of this study is its uniformity in enrolling patients with pRCC, which is important as retrospective studies have reflected heterogeneity in outcomes based on histologic subtypes undoubtedly in part due to differences in responses to currently available therapies.
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来源期刊
Kidney Cancer
Kidney Cancer Multiple-
CiteScore
0.90
自引率
8.30%
发文量
23
期刊最新文献
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