Comparison of the efficacy of sunitinib and pazopanib in patients with advanced non-clear renal cell carcinoma.

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Chemotherapy Pub Date : 2024-09-10 DOI:10.1080/1120009x.2024.2403051
Hasan Cagri Yildirim,Ertuğrul Bayram,Elvin Chalabiyev,Nargız Majidova,Tugay Avci,Halil Göksel Güzel,Caner Kapar,Mehmet Uzun,Perihan Perkin,Fahri Akgül,Saadet Sim Yildirim,Seda Sali,Anil Yildiz,Seher Nazli Kazaz,Engin Hendem,Murat Arcagok,Gulnihal Tufan,Umit Yildirim,Omer Faruk Akgul,Çagatay Arslan,Hakan Taban,Eren Sahin,Melek Caglayan,Ramazan Esen,Berna Öksüzoğlu,Deniz Can Guven,Muhammet Ali Kaplan,Murat Araz,Mert Basaran,Erdem Cubukcu,Erhan Gokmen,Irfan Cicin,Efnan Algin,Huseyin Salih Semiz,Deniz Tural,Banu Ozturk,Atike Pinar Erdogan,Murat Sari,Oguz Kara,Mustafa Erman
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Abstract

Non-clear cell renal cell carcinoma (non-ccRCC) is a highly heterogeneous disease group, accounting for approximately 25% of all RCC cases. Due to its rarity and especially heterogeneity, phase III trial data is limited and treatment options generally follow those of clear cell RCC. In the literature, there exists a number of studies with sunitinib, cabozantinib, and everolimus, but data on the efficacy of pazopanib are limited. Our aim in this study was to compare the efficacy of pazopanib and sunitinib, in a multicenter retrospective cohort of non-ccRCC patients. Our study included patients diagnosed with non-ccRCC who received pazopanib or sunitinib treatment as first-line therapy from 22 tertiary hospitals. We compared the progression-free survival (PFS), overall survival (OS), and response rates of pazopanib and sunitinib treatments. Additionally, we investigated prognostic factors in non-ccRCC. PFS and response rates of sunitinib and pazopanib were found to be similar, while a numerical difference was observed in OS. Being 65 years and older, being in the intermediate or poor risk group according to the International Metastatic Renal Cell Carcinoma Database Consortium, having liver metastases, presence of a sarcomatoid component, and having de novo metastatic disease were found to be significantly associated with shorter PFS. Pazopanib treatment appears to have similar efficacy in the treatment of non-ccRCC compared to sunitinib. Though randomized controlled trials are lacking and will probably be never be available, we suggest that pazopanib could be a preferred agent like sunitinib and cabozantinib.
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比较舒尼替尼和帕唑帕尼对晚期非透明肾细胞癌患者的疗效。
非透明细胞肾细胞癌(non-ccRCC)是一种高度异质性疾病,约占所有 RCC 病例的 25%。由于其罕见性,尤其是异质性,III 期试验数据有限,治疗方案通常沿用透明细胞 RCC 的治疗方案。在文献中,有一些关于舒尼替尼、卡博赞替尼和依维莫司的研究,但关于帕唑帕尼疗效的数据却很有限。本研究的目的是在非ccRCC患者的多中心回顾性队列中比较帕唑帕尼和舒尼替尼的疗效。我们的研究纳入了来自22家三级医院、接受帕唑帕尼或舒尼替尼一线治疗的非ccRCC患者。我们比较了帕唑帕尼和舒尼替尼治疗的无进展生存期(PFS)、总生存期(OS)和反应率。此外,我们还调查了非ccRCC的预后因素。结果发现,舒尼替尼和帕唑帕尼的治疗后生存期和反应率相似,而在治疗后生存期方面则存在数字差异。根据国际转移性肾细胞癌数据库联盟(International Metastatic Renal Cell Carcinoma Database Consortium),65岁及以上、中危或低危组、肝转移、肉瘤样成分和新发转移性疾病与较短的PFS显著相关。与舒尼替尼相比,帕唑帕尼治疗非ccRCC的疗效似乎相似。虽然目前还缺乏随机对照试验,而且很可能永远也不会有随机对照试验,但我们建议帕唑帕尼可以像舒尼替尼和卡博替尼一样成为首选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chemotherapy
Journal of Chemotherapy 医学-药学
CiteScore
3.70
自引率
0.00%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Chemotherapy is an international multidisciplinary journal committed to the rapid publication of high quality, peer-reviewed, original research on all aspects of antimicrobial and antitumor chemotherapy. The Journal publishes original experimental and clinical research articles, state-of-the-art reviews, brief communications and letters on all aspects of chemotherapy, providing coverage of the pathogenesis, diagnosis, treatment, and control of infection, as well as the use of anticancer and immunomodulating drugs. Specific areas of focus include, but are not limited to: · Antibacterial, antiviral, antifungal, antiparasitic, and antiprotozoal agents; · Anticancer classical and targeted chemotherapeutic agents, biological agents, hormonal drugs, immunomodulatory drugs, cell therapy and gene therapy; · Pharmacokinetic and pharmacodynamic properties of antimicrobial and anticancer agents; · The efficacy, safety and toxicology profiles of antimicrobial and anticancer drugs; · Drug interactions in single or combined applications; · Drug resistance to antimicrobial and anticancer drugs; · Research and development of novel antimicrobial and anticancer drugs, including preclinical, translational and clinical research; · Biomarkers of sensitivity and/or resistance for antimicrobial and anticancer drugs; · Pharmacogenetics and pharmacogenomics; · Precision medicine in infectious disease therapy and in cancer therapy; · Pharmacoeconomics of antimicrobial and anticancer therapies and the implications to patients, health services, and the pharmaceutical industry.
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