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了解舒尼替尼辅助治疗高危肾细胞癌 S-TRAC 试验的不良事件体验。

Understanding the adverse event experience in the S-TRAC adjuvant trial of sunitinib for high-risk renal cell carcinoma.

机构信息

Duke University Medical Center, Division of Oncology, 20 Duke Medicine Circle, Durham, NC 27710-4000, USA.

Pfizer Oncology, 235 E 42nd St, New York, NY 10017, USA.

出版信息

Future Oncol. 2020 Feb;16(4):39-47. doi: 10.2217/fon-2019-0369. Epub 2020 Jan 10.

Abstract

Until recently, the sole treatment for patients with nonmetastatic renal cell carcinoma (RCC) was nephrectomy followed by observation. As metastatic RCC (mRCC) remains largely incurable (5-year survival rate ∼12%), adjuvant treatment, with potential to prevent/delay disease recurrence, is needed. In November 2017, sunitinib was approved in the USA as the first adjuvant therapy for patients at high risk for recurrent RCC postnephrectomy based on results from the S-TRAC trial. Patients eligible for adjuvant treatment have no evidence of disease and may be less willing to tolerate side effects. Therefore, proactive adverse event management is critical for keeping patients on adjuvant treatment and requires understanding the subtle differences in the adverse event profile of sunitinib in the adjuvant versus metastatic RCC setting.

摘要

直到最近,非转移性肾细胞癌 (RCC) 患者的唯一治疗方法是肾切除术,然后观察。由于转移性 RCC (mRCC) 基本上无法治愈(5 年生存率约为 12%),因此需要辅助治疗,以预防/延迟疾病复发。2017 年 11 月,舒尼替尼在美国获得批准,成为 S-TRAC 试验结果基础上,用于肾切除术后复发风险高的 RCC 患者的首个辅助治疗药物。有资格接受辅助治疗的患者没有疾病证据,可能不太愿意忍受副作用。因此,积极主动的不良事件管理对于让患者接受辅助治疗至关重要,这需要了解舒尼替尼在辅助治疗和转移性 RCC 治疗环境中的不良事件特征的细微差异。

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