Immunotherapy Is Changing First-Line Treatment of Metastatic Renal-Cell Carcinoma

被引:40
作者
Labriola, Matthew K. [1 ]
Batich, Kristen A. [1 ]
Zhu, Jason [1 ]
McNamara, Megan A. [1 ]
Harrison, Michael R. [1 ]
Armstrong, Andrew J. [1 ]
George, Daniel J. [1 ]
Zhang, Tian [1 ]
机构
[1] Duke Canc Inst, Dept Med, Div Med Oncol, Durham, NC USA
关键词
Immune checkpoint inhibitors; Metastatic renal-cell carcioma; Targeted therapies; VEGF-immunotherapy combinations; VEGF therapies; REGULATORY T-CELLS; TUMOR-INFILTRATING LYMPHOCYTES; OPEN-LABEL; PERIPHERAL-BLOOD; INTERFERON-ALPHA; RANDOMIZED-TRIAL; POOR-PROGNOSIS; CLASS-I; SUNITINIB; SURVIVAL;
D O I
10.1016/j.clgc.2019.01.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The incidence of renal-cell carcinoma has been increasing each year, with nearly one third of new cases diagnosed at advanced or metastatic stage. The advent of targeted therapies for metastatic renal-cell carcinoma (mRCC) has underscored the need to subtype tumors according to tumor-immune expression profiles that may more reliably predict treatment outcomes. Over the past 2 decades, several vascular endothelial growth factor (VEGF) and tyrosine kinase inhibitors have been the mainstay for first- and second-line treatment of mRCC. Very recently, immunotherapy checkpoint inhibitors have significantly changed the treatment landscape for patients with mRCC, particularly for firstline treatment of intermediate to poor risk mRCC patients. Now, combination immunotherapy as well as combinations of immunotherapy with targeted agents can significantly alter disease outcomes. The field of immuno-oncology for mRCC has unveiled a deeper understanding of the immunoreactivity inherent to these tumors, and as a result combination therapy is evolving as a first-line modality. This review provides a timeline of advances and controversies in first-line treatment of mRCC, describes recent advances in understanding the immunoreactivity of these tumors, and addresses the future of combination anti-VEGF and immunotherapeutic platforms. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:E513 / E521
页数:9
相关论文
共 88 条
[1]
[Anonymous], 2017, J CLIN ONCOL
[2]
[Anonymous], NEW ENGL J MED
[3]
[Anonymous], ONCOTARGET
[4]
[Anonymous], 2017, ANN ONCOL, DOI DOI 10.1093/ANNONC/MDX371.002
[5]
[Anonymous], NCCN CAT EV CONS CAT
[6]
Everolimus versus sunitinib for patients with metastatic non-clear-cell renal cell carcinoma (ASPEN): a multicentre, open-label, randomised phase 2 trial [J].
Armstrong, Andrew J. ;
Halabi, Susan ;
Eisen, Tim ;
Broderick, Samuel ;
Stadler, Walter M. ;
Jones, Robert J. ;
Garcia, Jorge A. ;
Vaishampayan, Ulka N. ;
Picus, Joel ;
Hawkins, Robert E. ;
Hainsworth, John D. ;
Kollmannsberger, Christian K. ;
Logan, Theodore F. ;
Puzanov, Igor ;
Pickering, Lisa M. ;
Ryan, Christopher W. ;
Protheroe, Andrew ;
Lusk, Christine M. ;
Oberg, Sadie ;
George, Daniel J. .
LANCET ONCOLOGY, 2016, 17 (03) :378-388
[7]
Comparison of circulating and intratumoral regulatory T cells in patients with renal cell carcinoma [J].
Asma, Gati ;
Amal, Gorrab ;
Raja, Marrakchi ;
Amine, Derouiche ;
Mohammed, Chebil ;
Amel, Ben Ammar Elgaaied .
TUMOR BIOLOGY, 2015, 36 (05) :3727-3734
[8]
Axitinib in combination with pembrolizumab in patients with advanced renal cell cancer: a non-randomised, open-label, dose-finding, and dose-expansion phase 1b trial [J].
Atkins, Michael B. ;
Plimack, Elizabeth R. ;
Puzanov, Igor ;
Fishman, Mayer N. ;
McDermott, David F. ;
Cho, Daniel C. ;
Vaishampayan, Ulka ;
George, Saby ;
Olencki, Thomas E. ;
Tarazi, Jamal C. ;
Rosbrook, Brad ;
Fernandez, Kathrine C. ;
Lechuga, Mariajose ;
Choueiri, Toni K. .
LANCET ONCOLOGY, 2018, 19 (03) :405-415
[9]
The PD1:PD-L1/2 Pathway from Discovery to Clinical implementation [J].
Bardhan, Kankana ;
Anagnostou, Theodora ;
Boussiotis, Vassiliki A. .
FRONTIERS IN IMMUNOLOGY, 2016, 7
[10]
Angiogenic and immunological pathways in metastatic renal cell carcinoma: A counteracting paradigm or two faces of the same medal? The GIANUS Review [J].
Bracarda, Sergio ;
Porta, Camillo ;
Sabbatini, Roberto ;
Rivoltini, Licia .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2019, 139 :149-157