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Antitumor activity of nivolumab on hemodialysis after renal allograft rejection

BACKGROUND: Nivolumab (Opdivo™) is a novel IgG4 subclass programmed death-1 (PD-1) inhibiting antibody that has demonstrated breakthrough-designation anti-tumor activity. To date, clinical trials of nivolumab and other checkpoint inhibitors have generally excluded patients with solid organ transplan...

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Autores principales: Ong, Michael, Ibrahim, Andrea Marie, Bourassa-Blanchette, Samuel, Canil, Christina, Fairhead, Todd, Knoll, Greg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067882/
https://www.ncbi.nlm.nih.gov/pubmed/27777773
http://dx.doi.org/10.1186/s40425-016-0171-8
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author Ong, Michael
Ibrahim, Andrea Marie
Bourassa-Blanchette, Samuel
Canil, Christina
Fairhead, Todd
Knoll, Greg
author_facet Ong, Michael
Ibrahim, Andrea Marie
Bourassa-Blanchette, Samuel
Canil, Christina
Fairhead, Todd
Knoll, Greg
author_sort Ong, Michael
collection PubMed
description BACKGROUND: Nivolumab (Opdivo™) is a novel IgG4 subclass programmed death-1 (PD-1) inhibiting antibody that has demonstrated breakthrough-designation anti-tumor activity. To date, clinical trials of nivolumab and other checkpoint inhibitors have generally excluded patients with solid organ transplantation and patients with concurrent immunosuppression. However, organ transplant recipients are at high-risk of development of malignancy as a result of suppressed immune surveillance of cancer. CASE PRESENTATION: We illustrate the outcomes of a 63 year-old type I diabetic female patient who developed pulmonary metastatic, BRAF wild-type cutaneous melanoma 10 years after renal transplantation. After downward titration of the patient’s immunosuppressive medications and extensive multidisciplinary review, she was treated with nivolumab in the first-line setting. Within 1 week of administration, the patient experienced acute renal allograft rejection, renal failure and concurrent diabetic ketoacidosis due to steroid therapy. Allograft function did not return, but patient made a full clinical recovery after being placed on hemodialysis. Subsequently, the patient had clinical disease progression off therapy and required re-challenge with nivolumab on hemodialysis, resulting in ongoing clinical and radiographic response. CONCLUSIONS: This case illustrates multiple practical challenges and dangers of administering anti-PD1 immune checkpoint inhibitors to patients with solid-organ transplantation including need for titration of immunosuppressive medications, risks of allograft rejection, and treatment during hemodialysis.
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spelling pubmed-50678822016-10-24 Antitumor activity of nivolumab on hemodialysis after renal allograft rejection Ong, Michael Ibrahim, Andrea Marie Bourassa-Blanchette, Samuel Canil, Christina Fairhead, Todd Knoll, Greg J Immunother Cancer Case Report BACKGROUND: Nivolumab (Opdivo™) is a novel IgG4 subclass programmed death-1 (PD-1) inhibiting antibody that has demonstrated breakthrough-designation anti-tumor activity. To date, clinical trials of nivolumab and other checkpoint inhibitors have generally excluded patients with solid organ transplantation and patients with concurrent immunosuppression. However, organ transplant recipients are at high-risk of development of malignancy as a result of suppressed immune surveillance of cancer. CASE PRESENTATION: We illustrate the outcomes of a 63 year-old type I diabetic female patient who developed pulmonary metastatic, BRAF wild-type cutaneous melanoma 10 years after renal transplantation. After downward titration of the patient’s immunosuppressive medications and extensive multidisciplinary review, she was treated with nivolumab in the first-line setting. Within 1 week of administration, the patient experienced acute renal allograft rejection, renal failure and concurrent diabetic ketoacidosis due to steroid therapy. Allograft function did not return, but patient made a full clinical recovery after being placed on hemodialysis. Subsequently, the patient had clinical disease progression off therapy and required re-challenge with nivolumab on hemodialysis, resulting in ongoing clinical and radiographic response. CONCLUSIONS: This case illustrates multiple practical challenges and dangers of administering anti-PD1 immune checkpoint inhibitors to patients with solid-organ transplantation including need for titration of immunosuppressive medications, risks of allograft rejection, and treatment during hemodialysis. BioMed Central 2016-10-18 /pmc/articles/PMC5067882/ /pubmed/27777773 http://dx.doi.org/10.1186/s40425-016-0171-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Ong, Michael
Ibrahim, Andrea Marie
Bourassa-Blanchette, Samuel
Canil, Christina
Fairhead, Todd
Knoll, Greg
Antitumor activity of nivolumab on hemodialysis after renal allograft rejection
title Antitumor activity of nivolumab on hemodialysis after renal allograft rejection
title_full Antitumor activity of nivolumab on hemodialysis after renal allograft rejection
title_fullStr Antitumor activity of nivolumab on hemodialysis after renal allograft rejection
title_full_unstemmed Antitumor activity of nivolumab on hemodialysis after renal allograft rejection
title_short Antitumor activity of nivolumab on hemodialysis after renal allograft rejection
title_sort antitumor activity of nivolumab on hemodialysis after renal allograft rejection
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067882/
https://www.ncbi.nlm.nih.gov/pubmed/27777773
http://dx.doi.org/10.1186/s40425-016-0171-8
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