Modulation of the immune microenvironment of high-risk ductal carcinoma in situ by intralesional pembrolizumab injection.


Journal

NPJ breast cancer
ISSN: 2374-4677
Titre abrégé: NPJ Breast Cancer
Pays: United States
ID NLM: 101674891

Informations de publication

Date de publication:
25 May 2021
Historique:
received: 17 02 2020
accepted: 19 04 2021
entrez: 26 5 2021
pubmed: 27 5 2021
medline: 27 5 2021
Statut: epublish

Résumé

Ductal carcinoma in situ (DCIS) is a risk factor for the subsequent development of invasive breast cancer. High-risk features include age <45 years, size >5 cm, high-grade, palpable mass, hormone receptor negativity, and HER2 positivity. We have previously shown that immune infiltrates are positively associated with these high-risk features, suggesting that manipulating the immune microenvironment in high-risk DCIS could potentially alter disease progression. Patients with high-risk DCIS were enrolled in this 3 × 3 phase 1 dose-escalation pilot study of 2, 4, and 8 mg intralesional injections of the PD-1 immune checkpoint inhibitor, pembrolizumab. Study participants received two intralesional injections, three weeks apart, prior to surgery. Tissue from pre-treatment biopsies and post-treatment surgical resections was analyzed using multiplex immunofluorescence (mIF) staining for various immune cell populations. The intralesional injections were easily administered and well-tolerated. mIF analyses demonstrated significant increases in total T cell and CD8

Identifiants

pubmed: 34035311
doi: 10.1038/s41523-021-00267-z
pii: 10.1038/s41523-021-00267-z
pmc: PMC8149838
doi:

Types de publication

Journal Article

Langues

eng

Pagination

59

Subventions

Organisme : NCI NIH HHS
ID : T32 CA251070
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA196406
Pays : United States

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Auteurs

Alexa C Glencer (AC)

Department of Surgery, University of California San Francisco, San Francisco, CA, USA.

Jasmine M Wong (JM)

Department of Surgery, University of California San Francisco, San Francisco, CA, USA.

Nola M Hylton (NM)

Department of Surgery, University of California San Francisco, San Francisco, CA, USA.

Gregor Krings (G)

Department of Pathology, University of California San Francisco, San Francisco, CA, USA.

Emma McCune (E)

University of California San Francisco School of Medicine, San Francisco, CA, USA.

Harriet T Rothschild (HT)

University of California San Francisco School of Medicine, San Francisco, CA, USA.

Tristan A Loveday (TA)

Department of Surgery, University of California San Francisco, San Francisco, CA, USA.

Michael D Alvarado (MD)

Department of Surgery, University of California San Francisco, San Francisco, CA, USA.

Laura J Esserman (LJ)

Department of Surgery, University of California San Francisco, San Francisco, CA, USA.

Michael J Campbell (MJ)

Department of Surgery, University of California San Francisco, San Francisco, CA, USA. michael.campbell@ucsf.edu.

Classifications MeSH