TIM3 expression on TILs is associated with poor response to neoadjuvant chemotherapy in patients with locally advanced triple-negative breast cancer.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
06 Apr 2021
Historique:
received: 22 10 2020
accepted: 16 03 2021
entrez: 7 4 2021
pubmed: 8 4 2021
medline: 13 5 2021
Statut: epublish

Résumé

The expression of immune checkpoint receptors (ICRs) on tumor-infiltrating lymphocytes (TILs) is associated with better response to immunotherapies via immune checkpoint inhibitors. Therefore, we investigated various ICR expressions on TILs in patients with locally advanced triple-negative breast cancer (TNBC) after neoadjuvant chemotherapy (NAC). Expressions of ICRs were examined immunohistochemically in surgical specimens (n = 61) using monoclonal antibodies for PDL-1, PD-1, TIM-3, LAG-3, and CTLA-4. Positivity was defined as staining > 1% on TILs. The median age was 49 (24-76) years. The majority of patients were clinically T3-4 (n = 31, 50.8%) and clinically N1-3 (n = 58, 95.1%) before NAC. Of those, 82% were found to have CTLA-4 positivity, whereas PD1, PDL-1, LAG3, and TIM-3 expressions on TILs were 62.3, 50.9, 26.2, and 68.9%. A high expression of CTLA-4 was found to be associated with a better chemotherapy response (OR = 7.94, 95% CI: 0.9-70.12, p = 0.06), whereas TIM-3 positivity was contrarily associated with a worse chemotherapy response (OR = 0.253, 95% CI: 0.066-0.974, p = 0.047) as measured by the MDACC Residual Cancer Burden Index. At a 47-month follow-up, ypN0 (DFS; HR = 0.31, 95% CI: 0.12-0.83, p = 0.02 and DSS; HR = 0.21, 95% CI: 0.07-0.62, p = 0.005) and CTLA-4 high expression on TILs (DFS; HR = 0.38, 95% CI: 0.17-0.85, p = 0.019 and DSS; HR = 0.34, 95% CI: 0.15-0.78, p = 0.01) were found to be associated with improved survival. These findings demonstrate that CTLA-4, PD-1, PDL-1, and TIM-3 were highly expressed in TNBC. Based on these high expression patterns, further studies directed towards combined therapies are warranted in advanced TNBC in future.

Sections du résumé

BACKGROUND BACKGROUND
The expression of immune checkpoint receptors (ICRs) on tumor-infiltrating lymphocytes (TILs) is associated with better response to immunotherapies via immune checkpoint inhibitors. Therefore, we investigated various ICR expressions on TILs in patients with locally advanced triple-negative breast cancer (TNBC) after neoadjuvant chemotherapy (NAC).
METHODS METHODS
Expressions of ICRs were examined immunohistochemically in surgical specimens (n = 61) using monoclonal antibodies for PDL-1, PD-1, TIM-3, LAG-3, and CTLA-4. Positivity was defined as staining > 1% on TILs.
RESULTS RESULTS
The median age was 49 (24-76) years. The majority of patients were clinically T3-4 (n = 31, 50.8%) and clinically N1-3 (n = 58, 95.1%) before NAC. Of those, 82% were found to have CTLA-4 positivity, whereas PD1, PDL-1, LAG3, and TIM-3 expressions on TILs were 62.3, 50.9, 26.2, and 68.9%. A high expression of CTLA-4 was found to be associated with a better chemotherapy response (OR = 7.94, 95% CI: 0.9-70.12, p = 0.06), whereas TIM-3 positivity was contrarily associated with a worse chemotherapy response (OR = 0.253, 95% CI: 0.066-0.974, p = 0.047) as measured by the MDACC Residual Cancer Burden Index. At a 47-month follow-up, ypN0 (DFS; HR = 0.31, 95% CI: 0.12-0.83, p = 0.02 and DSS; HR = 0.21, 95% CI: 0.07-0.62, p = 0.005) and CTLA-4 high expression on TILs (DFS; HR = 0.38, 95% CI: 0.17-0.85, p = 0.019 and DSS; HR = 0.34, 95% CI: 0.15-0.78, p = 0.01) were found to be associated with improved survival.
CONCLUSIONS CONCLUSIONS
These findings demonstrate that CTLA-4, PD-1, PDL-1, and TIM-3 were highly expressed in TNBC. Based on these high expression patterns, further studies directed towards combined therapies are warranted in advanced TNBC in future.

Identifiants

pubmed: 33823818
doi: 10.1186/s12885-021-08054-6
pii: 10.1186/s12885-021-08054-6
pmc: PMC8025357
doi:

Substances chimiques

HAVCR2 protein, human 0
Hepatitis A Virus Cellular Receptor 2 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

357

Subventions

Organisme : Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi
ID : TTU-2017-26409
Organisme : Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi (TR)
ID : TOA-2017-27023
Organisme : Istanbul Breast Society
ID : not applicable

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Auteurs

Neslihan Cabioglu (N)

Department of General Surgery, Istanbul Medical Faculty, Breast Surgery Service, Istanbul University, Istanbul, Turkey. neslicab@yahoo.com.

Semen Onder (S)

Department of Pathology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.

Gizem Oner (G)

Department of General Surgery, Istanbul Medical Faculty, Breast Surgery Service, Istanbul University, Istanbul, Turkey.
Current Address: Multidisciplinary Oncologic Centre Antwerp (MOCA), Antwerp University Hospital, Edegem, Belgium.
Current Address: Center for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.

Hüseyin Karatay (H)

Department of Pathology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.

Mustafa Tukenmez (M)

Department of General Surgery, Istanbul Medical Faculty, Breast Surgery Service, Istanbul University, Istanbul, Turkey.

Mahmut Muslumanoglu (M)

Department of General Surgery, Istanbul Medical Faculty, Breast Surgery Service, Istanbul University, Istanbul, Turkey.

Abdullah İgci (A)

Department of General Surgery, Istanbul Medical Faculty, Breast Surgery Service, Istanbul University, Istanbul, Turkey.

Yeşim Eralp (Y)

Department of Medical Oncology, Institute of Oncology, Istanbul University, Istanbul, Turkey.
Acibadem Maslak Hospital, Acibadem Health Group, Istanbul, Turkey.

Adnan Aydiner (A)

Department of Medical Oncology, Institute of Oncology, Istanbul University, Istanbul, Turkey.

Pınar Saip (P)

Department of Medical Oncology, Institute of Oncology, Istanbul University, Istanbul, Turkey.

Ekrem Yavuz (E)

Department of Pathology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.

Vahit Ozmen (V)

Department of General Surgery, Istanbul Medical Faculty, Breast Surgery Service, Istanbul University, Istanbul, Turkey.

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