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Hyperprogressive disease in patients with advanced renal cell carcinoma: a new pattern of post-treatment cancer behavior.
Immunologic Research ( IF 4.4 ) Pub Date : 2020-07-10 , DOI: 10.1007/s12026-020-09138-4
Zhong Zheng 1 , Ke Wu 1 , Zhixian Yao 1 , Xingyu Mu 1 , Hantao Wu 1 , Weiguang Zhao 1 , Leilei Cheng 2 , Zhihong Liu 1
Affiliation  

Renal cell carcinoma (RCC) is among the most common cancers of the genitourinary system. Once RCC has progressed to a high tumor stage, surgery is no longer the optimal option, and treatment with drugs is more suitable. However, a proportion of patients with advanced RCC (aRCC) experience accelerated progression following targeted therapy or immunotherapy, a condition known as hyperprogressive disease (HPD). There is a growing body of literature that recognizes the importance of HPD. In the present review, thousands of studies that describe a variety of treatments for aRCC were identified in PubMed, Web of Science, and Cochrane Library and analyzed to establish the severity of clinical outcomes. Therefore, we managed to perform a review related to HPD of aRCC in these databases. It was found that 7~74% of patients advanced into progressive disease, 0~45% of patients died during post-treatment assessment, possibly due to fatal HPD. However, risk factors, mechanisms, and predictive factors are still not entirely clear. It is suggested that combination therapies might play a pivotal role in preventing HPD. Additional light needs to be shed on customization of therapies for aRCC after more data is collected and analyzed for HPD.



中文翻译:

晚期肾细胞癌患者的超进展性疾病:治疗后癌症行为的新模式。

肾细胞癌 (RCC) 是泌尿生殖系统最常见的癌症之一。一旦 RCC 进展到高肿瘤阶段,手术不再是最佳选择,药物治疗更合适。然而,一部分晚期 RCC (aRCC) 患者在靶向治疗或免疫治疗后出现加速进展,这种情况称为过度进展性疾病 (HPD)。越来越多的文献认识到 HPD 的重要性。在本综述中,在 PubMed、Web of Science 和 Cochrane Library 中确定了数千项描述 aRCC 各种治疗方法的研究,并对其进行了分析以确定临床结果的严重程度。因此,我们设法在这些数据库中进行了与 aRCC 的 HPD 相关的审查。结果发现,7~74%的患者进展为疾病进展,0~45% 的患者在治疗后评估期间死亡,可能是由于致命的 HPD。然而,危险因素、机制和预测因素仍不完全清楚。建议联合疗法可能在预防 HPD 中发挥关键作用。在为 HPD 收集和分析更多数据后,需要进一步阐明 aRCC 的疗法定制。

更新日期:2020-07-13
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