Immunotherapy: A new standard in the treatment of metastatic clear cell renal cell carcinoma.

Biomarkers Checkpoint inhibitors Immunotherapy Programmed cell death 1 receptor Renal cell carcinoma Tumor microenvironment

Journal

World journal of clinical oncology
ISSN: 2218-4333
Titre abrégé: World J Clin Oncol
Pays: United States
ID NLM: 101549149

Informations de publication

Date de publication:
24 Jan 2022
Historique:
received: 28 02 2021
revised: 16 09 2021
accepted: 11 12 2021
entrez: 4 2 2022
pubmed: 5 2 2022
medline: 5 2 2022
Statut: ppublish

Résumé

Renal cell cancer (RCC) represents 2%-3% of all adulthood cancers and is the most common malignant neoplasm of the kidney (90%). In the mid-nineties of the last century, the standard of treatment for patients with metastatic RCC was cytokines. Sunititib and pazopanib were registered in 2007 and 2009, respectively, and have since been the standard first-line treatment for metastatic clear cell RCC (mccRCC). Renal cell cancer is a highly immunogenic tumor with tumor infiltrating cells, including CD8+ T lymphocytes, dendritic cells, natural killer cells (NK) and macrophages. This observation led to the design of new clinical trials in which patients were treated with immunotherapy. With the growing evidence that proangiogenic factors can have immunomodulatory effects on the host's immune system, the idea of combining angiogenic drugs with immunotherapy has emerged, and new clinical trials have been designed. In the last few years, several therapeutic options have been approved [immunotherapy and immunotherapy/tyrosine kinase inhibitors (TKI)] for the first-line treatment of mccRCC. Nivolumab/ipilimumab is approved for the treatment of patients with intermediate and poor prognoses. Several checkpoint inhibitors (pembrolizumab, nivolumab, avelumab) in combination with TKI (axitinib, lenvatinib, cabozantinib) are approved for the treatment of patients regardless of their International mRCC Database Consortium prognostic group and PD-L1 expression. There is no specific and ideal biomarker that could help in selecting the ideal patient for the appropriate first-line treatment.

Identifiants

pubmed: 35116230
doi: 10.5306/wjco.v13.i1.28
pmc: PMC8790303
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

28-38

Informations de copyright

©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: Authors declare no conflict on interest.

Références

Lancet Oncol. 2018 Apr;19(4):451-460
pubmed: 29530667
J Clin Oncol. 2009 Dec 1;27(34):5794-9
pubmed: 19826129
N Engl J Med. 2019 Mar 21;380(12):1116-1127
pubmed: 30779529
J Clin Oncol. 2023 May 10;41(14):2493-2502
pubmed: 36809050
N Engl J Med. 2007 Jan 11;356(2):115-24
pubmed: 17215529
Cancer. 2008 Jul 15;113(2):293-301
pubmed: 18457330
N Engl J Med. 2019 Mar 21;380(12):1103-1115
pubmed: 30779531
Immunity. 2013 Jul 25;39(1):1-10
pubmed: 23890059
Nat Commun. 2016 Aug 30;7:12624
pubmed: 27571927
N Engl J Med. 2015 Nov 5;373(19):1803-13
pubmed: 26406148
ESMO Open. 2020 Nov;5(6):e001079
pubmed: 33246931
Curr Opin Urol. 2004 Jul;14(4):229-33
pubmed: 15205579
N Engl J Med. 2021 Apr 8;384(14):1289-1300
pubmed: 33616314
J Clin Oncol. 2010 Feb 20;28(6):1061-8
pubmed: 20100962
Clin Cancer Res. 2007 Mar 15;13(6):1757-61
pubmed: 17363529
Am J Surg Pathol. 2003 May;27(5):612-24
pubmed: 12717246
Cancer Sci. 2019 May;110(5):1564-1572
pubmed: 30861269
Science. 1993 May 28;260(5112):1317-20
pubmed: 8493574
JAMA Oncol. 2019 Oct 01;5(10):1411-1420
pubmed: 31343665
J Clin Oncol. 2019 Aug 10;37(23):2008-2016
pubmed: 31194611
Ann Transl Med. 2019 Nov;7(22):648
pubmed: 31930049
Ther Adv Med Oncol. 2020 Mar 18;12:1758835920907504
pubmed: 32215057
J Clin Oncol. 2015 Jun 10;33(17):1974-82
pubmed: 25605845
J Cancer. 2019 Jan 29;10(5):1154-1161
pubmed: 30854124
Cancer Immunol Res. 2016 Oct;4(10):820-822
pubmed: 27538576
Front Oncol. 2020 Jul 29;10:1321
pubmed: 32850419
J Immunother Cancer. 2018 Jan 29;6(1):9
pubmed: 29378660
Ann Transl Med. 2019 Sep;7(Suppl 6):S190
pubmed: 31656769
Cancer Immunol Res. 2018 Jul;6(7):758-765
pubmed: 29748390
Lancet. 2019 Jun 15;393(10189):2404-2415
pubmed: 31079938
Cancer Manag Res. 2018 Sep 11;10:3419-3431
pubmed: 30237743
Urol Oncol. 2015 Nov;33(11):496.e11-6
pubmed: 26210683
Cancer Treat Rev. 2008 May;34(3):193-205
pubmed: 18313224
Ann Oncol. 2020 Aug;31(8):1030-1039
pubmed: 32339648
World J Urol. 2016 Aug;34(8):1081-6
pubmed: 26847337
Clin Genitourin Cancer. 2019 Dec;17(6):e1147-e1152
pubmed: 31473121
N Engl J Med. 2018 Apr 05;378(14):1277-1290
pubmed: 29562145
Nat Rev Immunol. 2011 Sep 23;11(10):702-11
pubmed: 21941296
Nat Rev Cancer. 2008 Nov;8(11):865-73
pubmed: 18923434
Nature. 2013 Jul 4;499(7456):43-9
pubmed: 23792563
J Immunother Cancer. 2020 Mar;8(1):
pubmed: 32221016
Cancer Res. 2001 Jul 1;61(13):5132-6
pubmed: 11431351
Nature. 2013 Aug 22;500(7463):415-21
pubmed: 23945592
Future Oncol. 2017 Aug;13(19):1669-1671
pubmed: 28831825
Clin Genitourin Cancer. 2020 Dec;18(6):461-468.e3
pubmed: 32718906
J Clin Oncol. 2002 Jan 1;20(1):289-96
pubmed: 11773181
Genome Biol. 2016 Nov 17;17(1):231
pubmed: 27855702
Nat Genet. 2019 Feb;51(2):202-206
pubmed: 30643254
J Clin Oncol. 1993 Jul;11(7):1368-75
pubmed: 8315435
Lancet Oncol. 2018 Mar;19(3):405-415
pubmed: 29439857

Auteurs

Maja Popovic (M)

Department of Medical Oncology, Oncology Institute of Vojvodina, University of Novi Sad, Sremska Kamenica 21204, Serbia.

Gorana Matovina-Brko (G)

Department of Medical Oncology, Oncology Institute of Vojvodina, University of Novi Sad, Sremska Kamenica 21204, Serbia.

Masa Jovic (M)

Department of Medical Oncology, Oncology Institute of Vojvodina, University of Novi Sad, Sremska Kamenica 21204, Serbia.

Lazar S Popovic (LS)

Department of Medical Oncology, Oncology Institute of Vojvodina, University of Novi Sad, Sremska Kamenica 21204, Serbia.

Classifications MeSH