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
. 2018 Dec;9(6):1054-1062.
doi: 10.21037/jgo.2018.07.05.

Pilot evaluation of PD-1 inhibition in metastatic cancer patients with a history of liver transplantation: the Mayo Clinic experience

Affiliations

Pilot evaluation of PD-1 inhibition in metastatic cancer patients with a history of liver transplantation: the Mayo Clinic experience

Thomas T DeLeon et al. J Gastrointest Oncol. 2018 Dec.

Abstract

Background: Patients with solid organ transplants (SOTs) have been excluded from programmed death protein-1 (PD-1)/programmed death ligand-1 (PD-L1) inhibitor clinical trials due to concern for allograft rejection. The use of immune checkpoint inhibitor therapy remains controversial in transplant patients.

Methods: A retrospective pilot evaluation was conducted to assess the safety and efficacy of PD-1 inhibitors in patients with liver transplantation (LT). The primary endpoint was the rate of allograft rejection. Secondary endpoints included overall response rate (ORR), progression free survival (PFS) and overall survival (OS). Translational objectives included evaluation of tumor PD-L1, tumor infiltrating lymphocytes (TILs) and allograft PD-L1 expression.

Results: Seven metastatic cancer patients with a history of LT who received PD-1 inhibitor therapy were included [hepatocellular carcinoma (HCC), n=5; melanoma, n=2]. Rejection was observed in 2 of 7 patients. When rejection occurs it appears to be an early event with a median time to rejection of 24 days in our cohort. One patient achieved a complete response (CR), 3 patients had progressive disease (PD) and 3 patients discontinued therapy prior to restaging assessments. Two of five patients with available tissue had PD-L1 expression in the allograft and both developed rejection. One of five evaluable patients had abundant TILs. Two of five evaluable patients had PD-L1 tumor staining. The single patient with both abundant TILs and PD-L1 staining obtained a response. The median OS and PFS were 1.1 (0.3-21.1) and 1.8 (0.7-21.1) months, respectively.

Conclusions: In this pilot evaluation both preliminary efficacy (1 of 4) and allograft rejection (2 of 7) were exhibited in evaluable patients. Larger, prospective trials are needed to elucidate optimal patient selection.

Keywords: Immunotherapy; graft rejection; hepatocellular carcinoma (HCC); liver transplantation (LT); melanoma.

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest: The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
PET/CT scans of patient #2. (A) PET/CT prior to immunotherapy in patient #2; (B) PET/CT scan showing radiographic complete response in patient #2 after completing pembrolizumab treatment.
Figure 2
Figure 2
PD-L1 immunohistochemistry in liver allograft tissue near the portal vein in patient #6 (A) (magnification ×100) and patient #7 (B) (magnification ×200). Brown staining represents PD-L1 expression in portal lymphocytes. Image (B) shows enrichment of PD-L1 lymphocyte staining in areas of endotheliitis. *, denotes the portal vein. PD-L1, programmed death ligand-1.

References

    1. Dempke WCM, Fenchel K, Uciechowski P, et al. Second- and third-generation drugs for immuno-oncology treatment-The more the better? Eur J Cancer 2017;74:55-72. 10.1016/j.ejca.2017.01.001 - DOI - PubMed
    1. Riella LV, Watanabe T, Sage PT, et al. Essential role of PDL1 expression on nonhematopoietic donor cells in acquired tolerance to vascularized cardiac allografts. Am J Transplant 2011;11:832-40. 10.1111/j.1600-6143.2011.03451.x - DOI - PubMed
    1. Tanaka K, Albin MJ, Yuan X, et al. PDL1 is required for peripheral transplantation tolerance and protection from chronic allograft rejection. J Immunol 2007;179:5204-10. 10.4049/jimmunol.179.8.5204 - DOI - PMC - PubMed
    1. Ozkaynak E, Wang LQ, Goodearl A, et al. Programmed death-1 targeting can promote allograft survival. J Immunol 2002;169:6546-53. 10.4049/jimmunol.169.11.6546 - DOI - PubMed
    1. Ito T, Ueno T, Clarkson MR, et al. Analysis of the role of negative T cell costimulatory pathways in CD4 and CD8 T cell-mediated alloimmune responses in vivo. J Immunol 2005;174:6648-56. 10.4049/jimmunol.174.11.6648 - DOI - PubMed