Twelve cases of acneiform eruptions while on anti-CTLA4 therapy.


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 30 04 2019
accepted: 26 02 2020
pubmed: 10 3 2020
medline: 1 7 2020
entrez: 10 3 2020
Statut: ppublish

Résumé

We present the first detailed report of acneiform eruptions in patients on CTLA-4 inhibitor therapy. Acneiform eruptions commonly occur (up to 75-100%) as a cutaneous adverse event associated with EGFR inhibition; however, acneiform eruptions have not been highly reported as a cutaneous adverse event associated with CTLA-4 inhibitor therapy. We conducted a retrospective chart review of our institution's database to assess cutaneous adverse events associated with ipilimumab and tremelimumab, identifying 12 patients with acneiform eruptions (2 on tremelimumab and 10 on ipilimumab). The median time to onset of rash was 3 weeks after starting CTLA-4 inhibitor therapy, ranging from 0.7-45 weeks. Median time to cutaneous resolution was 6 weeks, ranging from 2 to 282 weeks. Treatment included oral and topical antibiotics, antihistamines, and oral or topical corticosteroids with four patients receiving no treatment. Acneiform eruptions are seen less commonly with CTLA-4 inhibitors than other cancer therapies, but awareness that it does occur is important for clinical practice. Better description is a necessary help to aid in early diagnosis and intervention. While EGFR inhibitor-associated acneiform eruptions are associated with clinical benefit, our sample size is too small to determine whether CTLA-4 inhibitor associated acneiform eruptions display the same correlation.

Identifiants

pubmed: 32147760
doi: 10.1007/s00520-020-05381-5
pii: 10.1007/s00520-020-05381-5
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Hormonal 0
CTLA-4 Antigen 0
CTLA4 protein, human 0
Ipilimumab 0
tremelimumab QEN1X95CIX

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2499-2502

Références

Lacouture ME, Wolchok JD, Yosipovitch G, Kähler KC, Busam KJ, Hauschild A (2014) Ipilimumab in patients with cancer and the management of dermatologic adverse events. J Am Acad Dermatol 71(1):161–169
doi: 10.1016/j.jaad.2014.02.035
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doi: 10.1684/ejd.2017.3023
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doi: 10.1002/cncr.24088
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Auteurs

Macartney Welborn (M)

University of Texas McGovern Medical School, Houston, TX, USA.

Shelby L Kubicki (SL)

University of Texas McGovern Medical School, Houston, TX, USA.

Naveen Garg (N)

University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, FCT 11.5000, Unit 1452, Houston, TX, 77030-4009, USA.

Anisha B Patel (AB)

University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, FCT 11.5000, Unit 1452, Houston, TX, 77030-4009, USA. APatel11@mdanderson.org.

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Classifications MeSH