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Case Reports
. 2025 Mar 17:15:1506324.
doi: 10.3389/fonc.2025.1506324. eCollection 2025.

Combined standard immunosuppression and immune checkpoint inhibition for BKPyV+ metastatic renal cell carcinoma of the graft in a kidney transplant recipient with chronic rejection: a case report

Affiliations
Case Reports

Combined standard immunosuppression and immune checkpoint inhibition for BKPyV+ metastatic renal cell carcinoma of the graft in a kidney transplant recipient with chronic rejection: a case report

Ilaria Gandolfini et al. Front Oncol. .

Abstract

We report on the first case of a dual-kidney transplant recipient diagnosed with a metastatic BK polyomavirus-positive clear renal cell carcinoma with sarcomatoid features, which caused extensive vena cava thrombosis. The patient was successfully treated with the immune checkpoint inhibitors (ICIs) ipilimumab plus nivolumab and continued immunosuppression with tacrolimus, mycophenolate, and steroids. He received ICIs despite the presence of graft dysfunction due to transplant glomerulopathy. As expected, the ICI treatment caused a progressive but asymptomatic decline of the graft function, which resulted in end-stage kidney disease. However, continuation of a full immunosuppression prevented acute rejection, graft intolerance syndrome episodes, or dual graft nephrectomy, which enabled the patient to successfully continue ICIs while on dialysis and to achieve sustained partial remission at the 17-month follow-up.

Keywords: BK polyomavirus; dialysis; immune checkpoint inhibitors; immunosuppression; kidney transplantation; renal cell carcinoma.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
(A, B) Basal contrast-enhanced CT of the pelvis and thorax at baseline. (A) Lobulated contrast-enhanced expansive lesion of approximately 12 cm in the left graft with extension in the context of the abdominal wall muscles (71 × 63 mm, red arrow). (B) Multiple parenchymal nodulations in both lungs suggestive for metastases, the largest of approximately 18 mm in the right lower lobe (blue arrows). (C, D) Contrast-enhanced CT of the pelvis and thorax at baseline 6 months post-immune checkpoint inhibitor (ICI) initiation. (C) Lobulated expansive lesion in the left graft (50 × 46 mm), with extension in the context of the abdominal wall muscles (42 × 22 mm). (D) Overall reduction of multiple parenchymal nodulations in both lungs. (E, F) Contrast-enhanced CT of the pelvis and thorax at baseline 17 months post-ICI initiation. (E) Stable lobulated expansive lesion in the left graft (43 × 39 mm), with extension in the context of the abdominal wall muscles (40 × 18 mm). (F) Overall lung progression, with increase of some pulmonary nodules, the largest of 14 mm at the upper left lobe and 15 mm at the right lower lobe.
Figure 2
Figure 2
Needle biopsy of the renal neoplasm (×4). Upper panel shows an undifferentiated carcinoma at hematoxylin and eosin stain (×4). Immunohistochemistry (IHC) was overall compatible with a clear cell carcinoma with sarcomatoid differentiation staining positive for CAIX, PAX8, and vimentin. Diffuse nuclear positivity for BKPyV SV40 by IHC was detected in neoplastic cells, while the surrounding healthy kidney tissue was negative.

References

    1. Maggiore U, Palmisano A, Buti S, Claire Giudice G, Cattaneo D, Giuliani N, et al. . Chemotherapy, targeted therapy and immunotherapy: Which drugs can be safely used in the solid organ transplant recipients? Transpl Int. (2021) 34:2442–58. doi: 10.1111/tri.v34.12 - DOI - PMC - PubMed
    1. Hellemans R, Pengel LHM, Choquet S, Maggiore U, for EWotTLJp . Managing immunosuppressive therapy in potentially cured post-kidney transplant cancer (excluding non-melanoma skin cancer): an overview of the available evidence and guidance for shared decision-making. Transpl Int. (2021) 34:1789–800. doi: 10.1111/tri.v34.10 - DOI - PMC - PubMed
    1. Tannir NM, Albiges L, McDermott DF, Burotto M, Choueiri TK, Hammers HJ, et al. . Nivolumab plus ipilimumab versus sunitinib for first-line treatment of advanced renal cell carcinoma: extended 8-year follow-up results of efficacy and safety from the phase III CheckMate 214 trial. Ann Oncol. (2024) 35:1026–38. doi: 10.1016/j.annonc.2024.07.727 - DOI - PMC - PubMed
    1. Carroll RP, Boyer M, Gebski V, Hockley B, Johnston JK, Kireta S, et al. . Immune checkpoint inhibitors in kidney transplant recipients: a multicentre, single-arm, phase 1 study. Lancet Oncol. (2022) 23:1078–86. doi: 10.1016/S1470-2045(22)00368-0 - DOI - PubMed
    1. Nguyen LS, Ortuno S, Lebrun-Vignes B, Johnson DB, Moslehi JJ, Hertig A, et al. . Transplant rejections associated with immune checkpoint inhibitors: A pharmacovigilance study and systematic literature review. Eur J Cancer. (2021) 148:36–47. doi: 10.1016/j.ejca.2021.01.038 - DOI - PubMed

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