Dupilumab for cancer-associated refractory pruritus.

IL-13 IL-31 IL-4 Oncologic pruritus chronic pruritus dupilumab itch

Journal

The journal of allergy and clinical immunology. Global
ISSN: 2772-8293
Titre abrégé: J Allergy Clin Immunol Glob
Pays: United States
ID NLM: 9918453488706676

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 10 02 2023
revised: 16 04 2023
accepted: 30 04 2023
medline: 2 10 2023
pubmed: 2 10 2023
entrez: 2 10 2023
Statut: epublish

Résumé

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. 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. 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. Biweekly treatment with dupilumab led to an immediate improvement in itching, which subsided entirely after a few doses without any significant adverse effects. 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.

Sections du résumé

Background UNASSIGNED
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 UNASSIGNED
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 UNASSIGNED
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 UNASSIGNED
Biweekly treatment with dupilumab led to an immediate improvement in itching, which subsided entirely after a few doses without any significant adverse effects.
Conclusion UNASSIGNED
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.

Identifiants

pubmed: 37779518
doi: 10.1016/j.jacig.2023.100128
pii: S2772-8293(23)00053-X
pmc: PMC10509917
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100128

Informations de copyright

© 2023 The Authors.

Références

J Allergy Clin Immunol. 2013 Aug;132(2):446-54.e5
pubmed: 23694808
Ann Dermatol. 2011 Nov;23(4):468-73
pubmed: 22148014
Allergy. 2021 Oct;76(10):2982-2997
pubmed: 33629401
Lancet. 2019 Nov 2;394(10209):1638-1650
pubmed: 31543428
J Allergy Clin Immunol. 2019 Jan;143(1):155-172
pubmed: 30194992
N Engl J Med. 2014 Jul 10;371(2):130-9
pubmed: 25006719
Dermatol Ther. 2010 Nov-Dec;23(6):590-6
pubmed: 21054705
Cell. 2017 Sep 21;171(1):217-228.e13
pubmed: 28890086
J Am Acad Dermatol. 2020 Jul;83(1):197-199
pubmed: 32229275
Acta Derm Venereol. 2016 Nov 2;96(7):894-898
pubmed: 27001482
Dermatol Clin. 2018 Jul;36(3):245-258
pubmed: 29929596
Support Care Cancer. 2019 Oct;27(10):3897-3904
pubmed: 30762144
Nat Immunol. 2004 Jul;5(7):752-60
pubmed: 15184896
Curr Ther Res Clin Exp. 2019 Oct 28;91:45-51
pubmed: 31871508
Br J Dermatol. 2019 Oct;181(4):761-769
pubmed: 30729499
Clin Exp Allergy. 2017 Apr;47(4):499-508
pubmed: 28000952

Auteurs

Aviv Talmon (A)

Allergy and Clinical Immunology Unit, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Shlomo Elias (S)

Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Limor Rubin (L)

Allergy and Clinical Immunology Unit, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Yaarit Ribak (Y)

Allergy and Clinical Immunology Unit, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Eyal Ben Dori (E)

Allergy and Clinical Immunology Unit, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Oded Shamriz (O)

Allergy and Clinical Immunology Unit, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Michal Lotem (M)

Sharett Institute of Oncology, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Irit Adini (I)

Harvard Medical School, Department of Surgery, Center for Engineering in Medicine and Surgery, Massachusetts General Hospital, Boston, Mass.

Yuval Tal (Y)

Allergy and Clinical Immunology Unit, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Classifications MeSH