Time on Therapy for at Least Three Months Correlates with Overall Survival in Metastatic Renal Cell Carcinoma

被引:25
作者
Chen, Viola J. [1 ]
Hernandez-Meza, Gabriela [2 ]
Agrawal, Prashasti [3 ]
Zhang, Chiyuan A. [4 ]
Xie, Lijia [5 ]
Gong, Cynthia L. [6 ,7 ]
Hoerner, Christian R. [1 ]
Srinivas, Sandy [1 ]
Oermann, Eric K. [8 ]
Fan, Alice C. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Div Oncol, Stanford, CA 94305 USA
[2] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[3] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Urol, Stanford, CA 94305 USA
[5] Highland Hosp, Dept Med, Oakland, CA 94602 USA
[6] Univ Southern Calif, Keck Sch Med, Dept Pediat, CHLA,Div Neonatol, Los Angeles, CA 90033 USA
[7] Univ Southern Calif, Keck Sch Med, Dept Pediat, CHLA,Fetal & Neonatal Inst, Los Angeles, CA 90033 USA
[8] Icahn Sch Med Mt Sinai, Dept Neurosurg, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
metastatic renal cell carcinoma; targeted kinase inhibitors; immunotherapy; systemic treatment; therapy sequencing; kidney cancer; RCC; IMDC criteria; favorable-; poor-; and intermediate-risk prognosis RCC; TYROSINE KINASE INHIBITORS; TARGETED THERAPY; INTERFERON-ALPHA; SUNITINIB; SORAFENIB; EVEROLIMUS;
D O I
10.3390/cancers11071000
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With 15 drugs currently approved for the treatment of metastatic renal cell carcinoma (mRCC) and even more combination regimens with immunotherapy on the horizon, there remains a distinct lack of molecular biomarkers for therapeutic efficacy. Our study reports on real-world clinical outcomes of mRCC patients from a tertiary academic medical center treated with empirically selected standard-of-care therapy. We utilized the Stanford Renal Cell Carcinoma Database (RCCD) to report on various outcome measures, including overall survival (OS) and the median number of lines of targeted therapies received from the time of metastatic diagnosis. We found that most metastatic patients did not survive long enough to attempt even half of the available targeted therapies. We also noted that patients who failed to receive a clinical benefit within the first two lines of therapy could still go on to experience clinical benefit in later lines of therapy. The term, "clinical benefit" was assigned to a line of therapy if a patient remained on drug treatment for three months or longer. Moreover, patients with clinical benefit in at least one line of therapy experienced significantly longer OS compared to those who did not have clinical benefit in at least one line of therapy. Developing biomarkers that identify patients who will receive clinical benefit in individual lines of therapy is one potential strategy for achieving rational drug sequencing in mRCC.
引用
收藏
页数:13
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