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Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients
BACKGROUND: Kidney transplant recipients (KTR) are at increased risk of cancer due to chronic immunosuppression. Non-melanoma skin cancer has an excess risk of approximately 250 times higher than the general population. Moreover, in solid organ transplant recipients (SOTR) these cancers have a more...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479765/ https://www.ncbi.nlm.nih.gov/pubmed/37675002 http://dx.doi.org/10.3389/fneph.2022.1041819 |
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author | Van Meerhaeghe, T. Baurain, J.F. Bechter, O. Orte Cano, C. Del Marmol, V. Devresse, A. Doubel, P. Hanssens, M. Hellemans, R. Lienard, D. Rutten, A. Sprangers, B. Le Moine, A. Aspeslagh, S. |
author_facet | Van Meerhaeghe, T. Baurain, J.F. Bechter, O. Orte Cano, C. Del Marmol, V. Devresse, A. Doubel, P. Hanssens, M. Hellemans, R. Lienard, D. Rutten, A. Sprangers, B. Le Moine, A. Aspeslagh, S. |
author_sort | Van Meerhaeghe, T. |
collection | PubMed |
description | BACKGROUND: Kidney transplant recipients (KTR) are at increased risk of cancer due to chronic immunosuppression. Non-melanoma skin cancer has an excess risk of approximately 250 times higher than the general population. Moreover, in solid organ transplant recipients (SOTR) these cancers have a more aggressive behavior, with an increased risk of metastasis and death. Cemiplimab, a human monoclonal IgG4 antibody against programmed cell death (PD-1) has shown considerable clinical activity in metastatic and locally advanced cutaneous squamous cell carcinoma (cSCC) in patients for whom no widely accepted standard of care exists. Cemiplimab has therefore been approved since 2018 for the treatment of advanced cSCC. However, data regarding the use of cemiplimab in SOTR and particularly in KTR are scarce and based on published case reports and small case series. In this study, we report on the real-life outcome of cemiplimab use in a Belgian cohort of seven KTR suffering from advanced cSCC. OBJECTIVE: To report on the overall response rate (ORR) and safety of cemiplimab in KTR in Belgium. RESULTS: Seven patients suffering from advanced cSCC, treated with cemiplimab, between 2018 and 2022, in Belgium were identified. Three patients were on corticosteroid monotherapy, one patient on tacrolimus monotherapy and three patients were on at least 2 immunosuppressants at start of cemiplimab. The ORR was 42.8%, stable disease was seen in 14.3% and progressive disease was found in 42.8% of the patients, respectively. The median administered number of cycles was 12, interquartile range (IQR) 25-75 [3.5 – 13.5]. All patients were treated with surgery before administration of cemiplimab, 71.4% received additional radiotherapy and only 1 patient was treated with chemotherapy prior to receiving cemiplimab. Biopsy-proven acute renal allograft rejection was observed in one patient, who eventually lost his graft function but showed a complete tumor response to treatment. Low grade skin toxicity was seen in one patient of the cohort. CONCLUSION: The present case series shows that the use of cemiplimab in KTR with advanced cSCC who failed to respond to previous surgery, chemo – and/or radiotherapy treatment is associated with an ORR of 42.8% with minimal risk of graft rejection (14.3%) and good tolerance. |
format | Online Article Text |
id | pubmed-10479765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104797652023-09-06 Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients Van Meerhaeghe, T. Baurain, J.F. Bechter, O. Orte Cano, C. Del Marmol, V. Devresse, A. Doubel, P. Hanssens, M. Hellemans, R. Lienard, D. Rutten, A. Sprangers, B. Le Moine, A. Aspeslagh, S. Front Nephrol Nephrology BACKGROUND: Kidney transplant recipients (KTR) are at increased risk of cancer due to chronic immunosuppression. Non-melanoma skin cancer has an excess risk of approximately 250 times higher than the general population. Moreover, in solid organ transplant recipients (SOTR) these cancers have a more aggressive behavior, with an increased risk of metastasis and death. Cemiplimab, a human monoclonal IgG4 antibody against programmed cell death (PD-1) has shown considerable clinical activity in metastatic and locally advanced cutaneous squamous cell carcinoma (cSCC) in patients for whom no widely accepted standard of care exists. Cemiplimab has therefore been approved since 2018 for the treatment of advanced cSCC. However, data regarding the use of cemiplimab in SOTR and particularly in KTR are scarce and based on published case reports and small case series. In this study, we report on the real-life outcome of cemiplimab use in a Belgian cohort of seven KTR suffering from advanced cSCC. OBJECTIVE: To report on the overall response rate (ORR) and safety of cemiplimab in KTR in Belgium. RESULTS: Seven patients suffering from advanced cSCC, treated with cemiplimab, between 2018 and 2022, in Belgium were identified. Three patients were on corticosteroid monotherapy, one patient on tacrolimus monotherapy and three patients were on at least 2 immunosuppressants at start of cemiplimab. The ORR was 42.8%, stable disease was seen in 14.3% and progressive disease was found in 42.8% of the patients, respectively. The median administered number of cycles was 12, interquartile range (IQR) 25-75 [3.5 – 13.5]. All patients were treated with surgery before administration of cemiplimab, 71.4% received additional radiotherapy and only 1 patient was treated with chemotherapy prior to receiving cemiplimab. Biopsy-proven acute renal allograft rejection was observed in one patient, who eventually lost his graft function but showed a complete tumor response to treatment. Low grade skin toxicity was seen in one patient of the cohort. CONCLUSION: The present case series shows that the use of cemiplimab in KTR with advanced cSCC who failed to respond to previous surgery, chemo – and/or radiotherapy treatment is associated with an ORR of 42.8% with minimal risk of graft rejection (14.3%) and good tolerance. Frontiers Media S.A. 2022-10-31 /pmc/articles/PMC10479765/ /pubmed/37675002 http://dx.doi.org/10.3389/fneph.2022.1041819 Text en Copyright © 2022 Van Meerhaeghe, Baurain, Bechter, Orte Cano, Del Marmol, Devresse, Doubel, Hanssens, Hellemans, Lienard, Rutten, Sprangers, Le Moine and Aspeslagh https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Nephrology Van Meerhaeghe, T. Baurain, J.F. Bechter, O. Orte Cano, C. Del Marmol, V. Devresse, A. Doubel, P. Hanssens, M. Hellemans, R. Lienard, D. Rutten, A. Sprangers, B. Le Moine, A. Aspeslagh, S. Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients |
title | Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients |
title_full | Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients |
title_fullStr | Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients |
title_full_unstemmed | Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients |
title_short | Cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients |
title_sort | cemiplimab for advanced cutaneous squamous cell carcinoma in kidney transplant recipients |
topic | Nephrology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479765/ https://www.ncbi.nlm.nih.gov/pubmed/37675002 http://dx.doi.org/10.3389/fneph.2022.1041819 |
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