Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Dec;3(12):1303-7.
doi: 10.1158/2326-6066.CIR-15-0150. Epub 2015 Aug 25.

PD-1 and PD-L1 Expression in Renal Cell Carcinoma with Sarcomatoid Differentiation

Affiliations

PD-1 and PD-L1 Expression in Renal Cell Carcinoma with Sarcomatoid Differentiation

Richard W Joseph et al. Cancer Immunol Res. 2015 Dec.

Abstract

Monoclonal antibodies that target the programmed death-1 (PD-1)-programmed death ligand-1 (PD-L1) axis have antitumor activity against multiple cancers. The presence of sarcomatoid differentiation in renal cell carcinoma (RCC) is associated with resistance to targeted therapy and poor responses to IL2 immunotherapy. Given the aggressive nature of RCC with sarcomatoid differentiation and the exclusion of sarcomatoid histology from metastatic RCC clinical trials, less is understood regarding selection of therapies. Here, we characterized the PD-1/PD-L1 axis in RCC with sarcomatoid differentiation. We directly compared two PD-L1 antibodies and found concordance of PD-L1 positivity in 89% of tested RCCs with sarcomatoid differentiation. Coexpression of PD-L1 on neoplastic cells and the presence of PD-1-positive tumor-infiltrating lymphocytes were identified in 50% (13 of 26) of RCCs with sarcomatoid differentiation. In contrast, only 1 of 29 clear cell RCCs (3%) had concurrent expression of PD-L1 and PD-1 (P = 0.002). Our study suggests that RCC with sarcomatoid differentiation may express PD-1/PD-L1 at a higher percentage than RCC without sarcomatoid differentiation, and patients with these tumors may be good candidates for treatment with anti-PD-1/PD-L1 therapies.

PubMed Disclaimer

Conflict of interest statement

Disclosure of Potential Conflicts of Interest

D. Bryant, Z. Gatalica, and S. Reddy are employees of Caris Life Sciences. S. Z. Millis is a former employee of Caris Life Sciences. N. J. Vogelzang is consultant to Roche/Genentech and to Caris Life Sciences. T. H. Ho, R. W. Joseph, E. M. Carballido, A. H. Bryce, M. L. Stanton, and E. P. Castle have no disclosures.

Figures

Figure 1
Figure 1
Representative PD-L1 Immunohistochemical Staining in Two Samples of RCC With Sarcomatoid Differentiation. A and B, Hematoxylin-eosin staining (H+E). C and D, Staining with SP142 anti–PD-L1 antibody showing positive (C) and negative staining (D). E and F, Staining with 130021 anti–PD-L1 antibody showing positive (E) and negative staining (F). Panels A, C, and E are from a PD-L1 positive RCC. Panels B, D, and F are from a PD-L1 negative RCC. All panels, original magnification ×20.
Figure 2
Figure 2
Representative Immunohistochemical Staining of PD-1 Expression in RCC With Sarcomatoid Features and Clear Cell RCC. Staining of sarcomatoid (A and C) and ccRCC (B and D) samples. A and B, Hematoxylin-eosin staining (H+E). C and D, Staining with anti–PD-1 antibody showing positive staining of sarcomatoid RCC (C) and negative staining of ccRCC (D). All panels, original magnification ×20. E, Percentage of tumors with PD-L1 expression (clone 130021), PD-1+ tumor-infiltrating lymphocytes, or coexpression of PD-L1 and PD-1 in sarcomatoid RCC or ccRCC.
Figure 3
Figure 3
PD-L1 Expression and Tumor Response to Anti–PD-1 Immunotherapy in a Patient With Metastatic RCC With Sarcomatoid Differentiation. A–C, Staining of biopsied tumor nodule with hematoxylin-eosin (A), with antibody SP142 to PD-L1 (B) or with antibody 130021 to PD-L1 (C). All panels, original magnification ×40. D and E, Serial computed tomographic imaging of biopsied tumor nodule (arrow) before (D) and after (E) initiation of pembrolizumab.

Similar articles

Cited by

References

    1. Herbst RS, Soria JC, Kowanetz M, Fine GD, Hamid O, Gordon MS, et al. Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients. Nature. 2014 Nov 27;515(7528):563–7. - PMC - PubMed
    1. Brahmer JR, Tykodi SS, Chow LQ, Hwu WJ, Topalian SL, Hwu P, et al. Safety and activity of anti-PD-L1 antibody in patients with advanced cancer. N Engl J Med. 2012 Jun 28;366(26):2455–65. Epub 2012 Jun 2. - PMC - PubMed
    1. Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, McDermott DF, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med. 2012 Jun 28;366(26):2443–54. Epub 2012 Jun 2. - PMC - PubMed
    1. Motzer RJ, Escudier B, Tomczak P, Hutson TE, Michaelson MD, Negrier S, et al. Axitinib versus sorafenib as second-line treatment for advanced renal cell carcinoma: overall survival analysis and updated results from a randomised phase 3 trial. Lancet Oncol. 2013 May;14(6):552–62. Epub 2013 Apr 16. Erratum in: Lancet Oncol. 2013 Jun;14(7):e254. - PubMed
    1. Shuch B, Said J, La Rochelle JC, Zhou Y, Li G, Klatte T, et al. Cytoreductive nephrectomy for kidney cancer with sarcomatoid histology: is up-front resection indicated and, if not, is it avoidable? J Urol. 2009 Nov;182(5):2164–71. Epub 2009 Sep 16. - PMC - PubMed

Publication types

MeSH terms