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Dupilumab for cancer-associated refractory pruritus
BACKGROUND: Pruritus can be an intolerable symptom in patients with cancer. Type 2 inflammation, and specifically, the cytokines IL-4, IL-13, and IL-31, play major roles in the itching process. Dupilumab is an antibody against IL-4Rα, which is a common IL-4 and IL-13 receptor subunit. Blocking IL-4...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509917/ https://www.ncbi.nlm.nih.gov/pubmed/37779518 http://dx.doi.org/10.1016/j.jacig.2023.100128 |
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author | Talmon, Aviv Elias, Shlomo Rubin, Limor Ribak, Yaarit Ben Dori, Eyal Shamriz, Oded Lotem, Michal Adini, Irit Tal, Yuval |
author_facet | Talmon, Aviv Elias, Shlomo Rubin, Limor Ribak, Yaarit Ben Dori, Eyal Shamriz, Oded Lotem, Michal Adini, Irit Tal, Yuval |
author_sort | Talmon, Aviv |
collection | PubMed |
description | BACKGROUND: Pruritus can be an intolerable symptom in patients with cancer. Type 2 inflammation, and specifically, the cytokines IL-4, IL-13, and IL-31, play major roles in the itching process. Dupilumab is an antibody against IL-4Rα, which is a common IL-4 and IL-13 receptor subunit. Blocking IL-4 and IL-13 activity reduces the synthesis of IL-31, the “itch cytokine,” and receptors for these 3 cytokines are expressed on itch nerves. Dupilumab is approved for treating moderate-to-severe atopic dermatitis, of which itching is a significant symptom. OBJECTIVE: The objective of this case study was to present the initial evidence of the safety and efficacy of dupilumab as a treatment for intractable malignancy-associated pruritus in 3 patients, thereby providing a basis for further investigation in a larger cohort. METHODS: As a proof of concept, we used dupilumab in our center to treat 3 patients with intractable malignancy-associated pruritus. The first patient was a 73-year-old male with a history of prostate cancer, the second patient was a 75-year-old female with cutaneous T-cell lymphoma, and the third patient was a 32-year-old male with metastatic melanoma. All 3 patients experienced debilitating itching, which started at some stage after the malignancy had been diagnosed. Moreover, none of the 3 patients showed clinical evidence of atopic dermatitis or other causes of itching (eg, uremia or liver failure), and none of the 3 patients responded to conventional treatments for pruritus. RESULTS: Biweekly treatment with dupilumab led to an immediate improvement in itching, which subsided entirely after a few doses without any significant adverse effects. CONCLUSION: We propose that dupilumab is a safe and effective treatment for intractable malignancy-associated pruritus, and we are currently testing it in a large cohort. |
format | Online Article Text |
id | pubmed-10509917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105099172023-09-29 Dupilumab for cancer-associated refractory pruritus Talmon, Aviv Elias, Shlomo Rubin, Limor Ribak, Yaarit Ben Dori, Eyal Shamriz, Oded Lotem, Michal Adini, Irit Tal, Yuval J Allergy Clin Immunol Glob Brief Report BACKGROUND: Pruritus can be an intolerable symptom in patients with cancer. Type 2 inflammation, and specifically, the cytokines IL-4, IL-13, and IL-31, play major roles in the itching process. Dupilumab is an antibody against IL-4Rα, which is a common IL-4 and IL-13 receptor subunit. Blocking IL-4 and IL-13 activity reduces the synthesis of IL-31, the “itch cytokine,” and receptors for these 3 cytokines are expressed on itch nerves. Dupilumab is approved for treating moderate-to-severe atopic dermatitis, of which itching is a significant symptom. OBJECTIVE: The objective of this case study was to present the initial evidence of the safety and efficacy of dupilumab as a treatment for intractable malignancy-associated pruritus in 3 patients, thereby providing a basis for further investigation in a larger cohort. METHODS: As a proof of concept, we used dupilumab in our center to treat 3 patients with intractable malignancy-associated pruritus. The first patient was a 73-year-old male with a history of prostate cancer, the second patient was a 75-year-old female with cutaneous T-cell lymphoma, and the third patient was a 32-year-old male with metastatic melanoma. All 3 patients experienced debilitating itching, which started at some stage after the malignancy had been diagnosed. Moreover, none of the 3 patients showed clinical evidence of atopic dermatitis or other causes of itching (eg, uremia or liver failure), and none of the 3 patients responded to conventional treatments for pruritus. RESULTS: Biweekly treatment with dupilumab led to an immediate improvement in itching, which subsided entirely after a few doses without any significant adverse effects. CONCLUSION: We propose that dupilumab is a safe and effective treatment for intractable malignancy-associated pruritus, and we are currently testing it in a large cohort. Elsevier 2023-06-23 /pmc/articles/PMC10509917/ /pubmed/37779518 http://dx.doi.org/10.1016/j.jacig.2023.100128 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Brief Report Talmon, Aviv Elias, Shlomo Rubin, Limor Ribak, Yaarit Ben Dori, Eyal Shamriz, Oded Lotem, Michal Adini, Irit Tal, Yuval Dupilumab for cancer-associated refractory pruritus |
title | Dupilumab for cancer-associated refractory pruritus |
title_full | Dupilumab for cancer-associated refractory pruritus |
title_fullStr | Dupilumab for cancer-associated refractory pruritus |
title_full_unstemmed | Dupilumab for cancer-associated refractory pruritus |
title_short | Dupilumab for cancer-associated refractory pruritus |
title_sort | dupilumab for cancer-associated refractory pruritus |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509917/ https://www.ncbi.nlm.nih.gov/pubmed/37779518 http://dx.doi.org/10.1016/j.jacig.2023.100128 |
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