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Pancreatic adverse events in patients treated with immune checkpoint inhibitors
BACKGROUND AND AIM: The inhibition of cytotoxic T‐lymphocyte associated antigen‐4 (CTLA‐4) and programmed cell death‐1 (PD‐1) has been a target for multiple drugs to enhance the T‐cell antitumor activity. However, these immune checkpoint inhibitors (ICIs) come with a panel of immune‐related adverse...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Publishing Asia Pty Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037034/ https://www.ncbi.nlm.nih.gov/pubmed/36968572 http://dx.doi.org/10.1002/jgh3.12875 |
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author | Hana, Caroline Rehman, Tauseef Park, Kyeeun Carracedo Uribe, Carlos Aung, Pyi Phyo Hunis, Brian Salzberg, Matthew Zikria, Jennifer Hussein, Atif |
author_facet | Hana, Caroline Rehman, Tauseef Park, Kyeeun Carracedo Uribe, Carlos Aung, Pyi Phyo Hunis, Brian Salzberg, Matthew Zikria, Jennifer Hussein, Atif |
author_sort | Hana, Caroline |
collection | PubMed |
description | BACKGROUND AND AIM: The inhibition of cytotoxic T‐lymphocyte associated antigen‐4 (CTLA‐4) and programmed cell death‐1 (PD‐1) has been a target for multiple drugs to enhance the T‐cell antitumor activity. However, these immune checkpoint inhibitors (ICIs) come with a panel of immune‐related adverse events (irAEs) that include mainly endocrine, skin, and gastrointestinal effects. We report seven cases of pancreatic irAEs in patients treated with ICIs at our institute. METHODS: This is a case series; data was collected through chart review by 3 different data collectors and was analyzed separately by 2 physicians. RESULTS: Of these seven cases, two had diabetic ketoacidosis (DKA), while five had pancreatitis diagnosed by a substantial rise in serum lipase. Pancreatitis was asymptomatic in two cases. A pancreatic biopsy in one case revealed type 2 autoimmune pancreatitis. The ICIs used included pembrolizumab, nivolumab, durvalumab, and avelumab. Treatment included steroids and holding the ICI therapy: three cases had complete resolution of pancreatitis while two cases required either a prolonged taper or a second course of prednisone for recurrence of pancreatitis. On the other hand, the DKA cases were treated with withdrawal of the ICI and starting insulin with no steroid therapy. CONCLUSIONS: Pancreatitis and DKA are rare adverse events of ICIs that can be controlled by holding the ICI with or without starting steroids. Rechallenging the patient with the same ICI is possible in selected cases. |
format | Online Article Text |
id | pubmed-10037034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wiley Publishing Asia Pty Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-100370342023-03-25 Pancreatic adverse events in patients treated with immune checkpoint inhibitors Hana, Caroline Rehman, Tauseef Park, Kyeeun Carracedo Uribe, Carlos Aung, Pyi Phyo Hunis, Brian Salzberg, Matthew Zikria, Jennifer Hussein, Atif JGH Open Original Articles BACKGROUND AND AIM: The inhibition of cytotoxic T‐lymphocyte associated antigen‐4 (CTLA‐4) and programmed cell death‐1 (PD‐1) has been a target for multiple drugs to enhance the T‐cell antitumor activity. However, these immune checkpoint inhibitors (ICIs) come with a panel of immune‐related adverse events (irAEs) that include mainly endocrine, skin, and gastrointestinal effects. We report seven cases of pancreatic irAEs in patients treated with ICIs at our institute. METHODS: This is a case series; data was collected through chart review by 3 different data collectors and was analyzed separately by 2 physicians. RESULTS: Of these seven cases, two had diabetic ketoacidosis (DKA), while five had pancreatitis diagnosed by a substantial rise in serum lipase. Pancreatitis was asymptomatic in two cases. A pancreatic biopsy in one case revealed type 2 autoimmune pancreatitis. The ICIs used included pembrolizumab, nivolumab, durvalumab, and avelumab. Treatment included steroids and holding the ICI therapy: three cases had complete resolution of pancreatitis while two cases required either a prolonged taper or a second course of prednisone for recurrence of pancreatitis. On the other hand, the DKA cases were treated with withdrawal of the ICI and starting insulin with no steroid therapy. CONCLUSIONS: Pancreatitis and DKA are rare adverse events of ICIs that can be controlled by holding the ICI with or without starting steroids. Rechallenging the patient with the same ICI is possible in selected cases. Wiley Publishing Asia Pty Ltd 2023-02-06 /pmc/articles/PMC10037034/ /pubmed/36968572 http://dx.doi.org/10.1002/jgh3.12875 Text en © 2023 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Hana, Caroline Rehman, Tauseef Park, Kyeeun Carracedo Uribe, Carlos Aung, Pyi Phyo Hunis, Brian Salzberg, Matthew Zikria, Jennifer Hussein, Atif Pancreatic adverse events in patients treated with immune checkpoint inhibitors |
title | Pancreatic adverse events in patients treated with immune checkpoint inhibitors |
title_full | Pancreatic adverse events in patients treated with immune checkpoint inhibitors |
title_fullStr | Pancreatic adverse events in patients treated with immune checkpoint inhibitors |
title_full_unstemmed | Pancreatic adverse events in patients treated with immune checkpoint inhibitors |
title_short | Pancreatic adverse events in patients treated with immune checkpoint inhibitors |
title_sort | pancreatic adverse events in patients treated with immune checkpoint inhibitors |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037034/ https://www.ncbi.nlm.nih.gov/pubmed/36968572 http://dx.doi.org/10.1002/jgh3.12875 |
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