[Immunohistochemical study of MSI markers in breast cancer].
Autor: | Kuznetsova OA; Russian Medical Academy of Continuous Professional Education of the Ministry of Health of Russia, Moscow, Russia., Zavalishina LE; Russian Medical Academy of Continuous Professional Education of the Ministry of Health of Russia, Moscow, Russia., Andreeva YY; Russian Medical Academy of Continuous Professional Education of the Ministry of Health of Russia, Moscow, Russia., Vinogradov MI; Regional Clinical Oncology Dispensary, Ryazan, Russia., Shomova MV; Regional Clinical Oncology Dispensary, Ryazan, Russia., Frank GA; Russian Medical Academy of Continuous Professional Education of the Ministry of Health of Russia, Moscow, Russia. |
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Jazyk: | ruština |
Zdroj: | Arkhiv patologii [Arkh Patol] 2021; Vol. 83 (1), pp. 12-17. |
DOI: | 10.17116/patol20218301112 |
Abstrakt: | Objective: To investigate the expression of microsatellite instability (MSI) markers, which is detected by an immunohistochemical technique, and to compare the expression with the PD-L1 status in luminal B, HER2-negative and triple-negative breast cancer. Material and Methods: The investigation included tumors from 40 patients with triple-negative and luminal B, HER2-negative subtypes. Immunohistochemical study was performed using Ventana antibodies: anti-MLH1 (clone M1), anti-MSH2 (clone G219-1129), anti-PMS2 (clone A16-4), and anti-MSH6 (clone SP93). MSI was assessed according to the standard criteria. Results: The PD-L1-positive status was present in 14 (35%) of the 40 patients. Moreover, MSI-H was detected in only 1 (2.50%) case. The two-year survival rate was 87.5%; it should be noted that the median survival rate was not reached either in the study sample or in the groups divided according to PD-L1 and MSI statuses. The overall survival rate for patients with MSI was 75% (3/4). Conclusion: The first comparative study of the expression of PD-L1 and immunohistochemical MSI markers, which has been conducted on a small sample, fails to draw unambiguous conclusions, but shows the need to investigate this phenomenon on large samples and by using genetic methods. |
Databáze: | MEDLINE |
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