Ipilimumab in combination with nivolumab for the treatment of renal cell carcinoma

被引:52
作者
Gao, Xin [1 ]
McDermott, David F. [2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[2] Beth Israel Deaconess Med Ctr, Biol Therapy Program, 330 Brookline Ave, Boston, MA 02215 USA
[3] Beth Israel Deaconess Med Ctr, Cutaneous Oncol Program, 330 Brookline Ave, Boston, MA 02215 USA
关键词
CTLA-4; immune checkpoint therapy; ipilimumab; kidney cancer; nivolumab; PD-1; renal cell carcinoma; INTERFERON-ALPHA; DOUBLE-BLIND; SPONTANEOUS REGRESSION; PULMONARY METASTASES; TARGETED THERAPY; END-POINTS; OPEN-LABEL; TRIAL; SUNITINIB; SURVIVAL;
D O I
10.1080/14712598.2018.1513485
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Renal cell carcinoma (RCC) is a highly immunogenic neoplasm, and cytokine-based immunotherapies have been used for decades with limited success. In recent years, antibody-based immunotherapies targeting immune checkpoint receptors PD-1 and CTLA-4 have demonstrated clinical efficacy in metastatic RCC (mRCC) patients, leading to FDA approval of the combination of nivolumab and ipilimumab in treatment-naive patients with intermediate- or poor-risk disease in April 2018.Areas covered: The pharmacodynamics and pharmacokinetics of nivolumab and ipilimumab are reviewed. Clinical safety and efficacy results from pivotal phase I and III trials of the combination of nivolumab plus ipilimumab in mRCC are summarized, and the combination is reviewed in the context of other available systemic therapies for RCC. Ongoing clinical studies involving the combination of nivolumab plus ipilimumab in RCC are discussed.Expert opinion: The combination of nivolumab and ipilimumab has demonstrated superior efficacy for treatment-naive patients with intermediate- and poor-risk mRCC with clear cell histology and is likely to replace anti-angiogenic therapies as the treatment-of-choice in this patient population in the United States. Development of additional combination strategies, novel trial designs, and predictive biomarkers of response will be important to further optimize therapeutic selection and clinical outcomes.
引用
收藏
页码:947 / 957
页数:11
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