ORIGINAL ARTICLE
PD-L1 expression in triple-negative breast cancer: a cross-sectional study in a Polish population
 
More details
Hide details
1
Department of Tumor Pathology and Pathomorphology, Oncology Center, Prof. Franciszek £ukaszczyk Memorial Hospital, Bydgoszcz, Poland
 
2
Chair of Clinical Pathomorphology, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, Bydgoszcz, Poland
 
3
Chair and Department of Oncologic Pathology and Prophylaxis, Greater Poland Cancer Center, Poznañ University of Medical Sciences and Department of Oncologic Pathology, Poznan, Poland
 
4
Department of Pathology, Maria Sk³odowska-Curie Memorial Cancer Centre and Institute of Oncology, Warsaw, Poland
 
 
Submission date: 2020-06-07
 
 
Final revision date: 2020-11-29
 
 
Acceptance date: 2020-12-28
 
 
Publication date: 2021-02-22
 
 
Pol J Pathol 2020;71(4):301-306
 
KEYWORDS
TOPICS
ABSTRACT
Triple-negative breast cancer (TNBC) accounts for 15-20% of all breast carcinomas and represents an aggressive variant with a high mortality rate. PD-L1 is a protein that plays a pivotal role in suppressing the adaptive immune system. It has become a central target of the immunotherapy approach. Determining the PD-L1 status can identify TNBC patients who may benefit from targeted therapy. This study was performed to estimate the prevalence of PD-L1 expression among Polish TNBC patients. A total of 123 patients with TNBC were tested for PD-L1 expression using immunohistochemical studies. The PD-L1-positive tumors were found in 55 patients (45%), while PD-L1-negative tumors were found in 68 patients (55%). The PD-L1 positive tumors included 17 patients (31%) with the expression covering up to 1% of tumor area, 23 patients (42%) covering 2-5%, 8 patients (14%) covering 6-10% and 7 patients (13%) covering more than 10% of tumor area. The PD-L1 negative tumors included 17 patients (25%) with the expression covering less than 1% of tumor area and 51 patients (75%) with a complete lack of expression. There were no significant differences between the groups with different status of PD-L1 and the clinical tumor and lymph node stages as well as the patients’ age.
REFERENCES (34)
1.
Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin 2018; 68: 7-30.
 
2.
Luo L, Zhang J, Tang H, et al. LncRNA SNORD3A specifically sensitizes breast cancer cells to 5-FU by sponging miR-185-5p to enhance UMPS expression. Cell Death Dis 2020; 11: 329.
 
3.
Marra A, Viale G, Curigliano G. Recent advances in triple negative breast cancer: The immunotherapy era. BMC Med 2019; 17: 1-9.
 
4.
Zhang M, Sun H, Zhao S, et al. Expression of PD-L1 and prognosis in breast cancer: A metaanalysis. Oncotarget 2017; 8: 31347-31354.
 
5.
Schmolze D, Behrendt CE, Lee PP, et al. The Prognostic Value of PD-L1 Expression in Triple-Negative Breast Cancer: A Cohort Study and Systematic Literature Review 2019; 1: 37-44.
 
6.
Dogukan R, Ucak R, Dogukan FM, et al. Correlation between the Expression of PD-L1 and Clinicopathological Parameters in Triple Negative Breast Cancer Patients. Eur J Breast Heal 2019; 15: 235-241.
 
7.
Mavaddat N, Rebbeck TR, Lakhani SR, et al. Incorporating tumour pathology information into breast cancer risk prediction algorithms. Breast Cancer Res 2010; 12: 1-12.
 
8.
Hammond MEH, Hayes DF, Dowsett M, et al. American Society of Clinical Oncology/College of American Pathologists Guideline Recommendations for Immunohistochemical Testing of Estrogen and Progesterone Receptors in Breast Cancer.
 
9.
J Clin Oncol 2010; 28: 2784-2795.
 
10.
Wolff AC, Hammond MEH, Hicks DG, et al. Recommendations for Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Update. J Clin Oncol 2013; 31: 3997-4013.
 
11.
Muenst S, Schaerli AR, Gao F, et al. Expression of programmed death ligand 1 (PD-L1) is associated with poor prognosis in human breast cancer. Breast Cancer Res Treat 2014; 146: 15-24.
 
12.
Ribas A, Wolchok JD. Cancer immunotherapy using checkpoint blockade. Science 2018; 359: 1350-1355.
 
13.
KöY Y, Dirilenoglu F, Tetikkurt ÜS, et al. Aldehyde dehydrogenase-1 positivity is associated with er negativity in patients with invasive ductal carcinoma of the breast. Pol J Pathol 2020; 71: 254-260.
 
14.
Tuzimek A, Fudalej MM, Sobiborowicz A, et al. Incorporating immunohistochemical markers into screening methods for BRCA1-mutated breast cancer. PolJ Pathol 2020; 71: 261-269.
 
15.
Marsza³ek A, Szylberg £, Wiœniewska E, et al. Impact of COX-2,.
 
16.
IL-1β, TNF-α, IL-4 and IL-10 on the process of carcinogenesisin the large bowel. Polish J Pathol 2012; 4: 221-227.
 
17.
Emens LA, Cruz C, Eder JP, et al. Long-term Clinical Outcomes and Biomarker Analyses of Atezolizumab Therapy for Patients with Metastatic Triple-Negative Breast Cancer: A Phase 1 Study. JAMA Oncol 2019; 5: 74-82.
 
18.
Vennapusa B, Baker B, Kowanetz M, et al. Development of a PD-L1 Complementary Diagnostic Immunohistochemistry Assay (SP142) for Atezolizumab. Appl Immunohistochem Mol Morphol 2019; 27: 92-100.
 
19.
Patel SP, Kurzrock R. PD-L1 Expression as a Predictive Biomarker in Cancer Immunotherapy. Mol Cancer Ther 2015; 14: 847-856.
 
20.
Ilie M, Hofman V, Dietel M, et al. Assessment of the PD-L1 status by immunohistochemistry: challenges and perspectives for therapeutic strategies in lung cancer patients. Virchows Arch 2016; 468: 511-525.
 
21.
Reck M, Rodríguez-Abreu D, Robinson AG, et al. Pembrolizumab versus Chemotherapy for PD-L1-Positive Non-Small-Cell Lung Cancer. N Engl J Med 2016; 375: 1823-1833.
 
22.
Schmid P, Adams S, Rugo HS, et al. Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer.
 
23.
N Engl J Med 2018; 379: 2108-2121.
 
24.
Gil Del Alcazar CR, Huh SJ, Ekram MB, et al. Immune Escape in Breast Cancer During In Situ to Invasive Carcinoma Transition. Cancer Discov 2017; 7: 1098-1115.
 
25.
Eggermont AMM, Chiarion-Sileni V, Grob JJ, et al. Prolonged Survival in Stage III Melanoma with Ipilimumab Adjuvant Therapy. N Engl J Med 2016; 375: 1845-1855.
 
26.
Weber J, Mandala M, Del Vecchio M, et al. Adjuvant Nivolumab.
 
27.
versus Ipilimumab in Resected Stage III or IV Melanoma. N Engl J Med 2017; 377: 1824-1835.
 
28.
Antonia SJ, Villegas A, Daniel D, et al. Overall Survival with Durvalumab after Chemoradiotherapy in Stage III NSCLC.
 
29.
N Engl J Med 2018; 379: 2342-2350.
 
30.
Pehlivan FS, Sivrikoz ON, Dag F, et al. Distribution of CXCR4 and tumour-infiltrating lymphoc ytes in breast cancer subtypes; their relationship with each other, axillary lymph node involvement, and other prognostic indicators. Polish J Pathol 2018; 69: 335-341.
 
31.
Brahmer J, Reckamp KL, Baas P, et al. Nivolumab versus Docetaxel in Advanced Squamous-Cell Non-Small-Cell Lung Cancer. N Engl J Med 2015; 373: 123-135.
 
32.
Rittmeyer A, Barlesi F, Waterkamp D, et al. Atezolizumab versus docetaxel in patients with previously treated non-small-cell lung cancer (OAK): a phase 3, open-label, multicentre randomised controlled trial. Lancet 2017; 389: 255-265.
 
33.
Motzer RJ, Escudier B, McDermott DF, et al. Nivolumab versus Everolimus in Advanced Renal-Cell Carcinoma. N Engl.
 
34.
J Med 2015; 373: 1803-1813.
 
eISSN:2084-9869
ISSN:1233-9687
Journals System - logo
Scroll to top