DOI: 10.25881/BPNMSC.2019.24.68.009

Authors

Puchkova O.S.1, Sinicyn V.E.2, Bogomazova S.Yu.3, Mershina E.A.2, Shirokij V.P.3, Bazhenova D.A.2, Nenajdenko E.V.2

1 Haddassah Medical Skolkovo, Moscow

2 FFM Lomonosov Moscow State University, Moscow

3 Federal Center of Medicine and Rehabilitation, Moscow

Abstract

To identify the presence of a correlation between the size, histology subtype of breast cancer and the tumor grade. In this study, 169 patients. All patients underwent a core biopsy with subsequent histological examination, and were divided into 2 groups. The first group consisted of 57 women (33.7%) with tumors arising in the terminal ductal-lobular unit - acinar adenocarcinoma (AAB) unifocal and multifocal forms, and the second group - 112 women (66.3%) with types of ductal adenocarcinoma in situ (in situ DAB) and ductal adenocarcinoma in situ associated with the acinar form of breast cancer (DAB + AAB). Evaluation of the breast density was made using ACR 2013 classification. The tumor size was measured on mammography and postoperative histology. The result of our study suggests the size of breast cancer of acinar origin do not associated with the component in situ, which accounts for 75% of the detected cancers in mammography, correlates with the degree of malignancy - the larger the tumor size, the higher the degree of malignancy, which confirms the data on the possible dedifferentiation of tumor cells during its growth. The degree of malignancy of breast cancer is one of the important predictors of long-term prognosis of treatment. Thus, the tumor size determined by mammography can be an independent prognostic factor already at the stage of diagnosis. Conclusions. The size of the breast cancer of acinar origin, determined at the time of diagnosis on mammography, correlates with the tumor Grade and can be an independent prognostic factor of the long-term patient outcome.

Keywords: breast cancer, mammography, long-term outcome, tumor grade.

References

1. Abelev, G.I. Mekhanizmy differencirovki i opuholevyj rost//. Biohimiya. 2000; 65(1): 127–128.

2. Semiglazov, V.F. Hirurgicheskoe lecheniya raka molochnoj zhelezy (istoriya i sovremennost’). // Prakticheskaya onkologiya 2002; 3 (1): 21– 27.

3. Choi, Y., Lee, H.J., Jang, M.H., Gwak, J.M., Lee, K.S., Kim, E.J., Kim, H.J., Lee, H.E., Park, S.Y. Epithelial-mesenchymal transition increases during the progression of in situ to invasive basal-like breast cancer. // Human Pathology, 2013 Volume 44, Issue 11, 2581–2589.

4. Gabbert, H., Wagner, R., Moll, R., Gerharz, C.D. Tumor dedifferentiation: an important step in tumor invasion. // Clin Exp Metastasis. 1985 Oct-Dec; 3(4): 257–279.

5. James E. Bradner, Denes Hnisz, Richard A. Young, Transcriptional Addiction in Cancer // Cell, Volume 168, Issue 4, 2017, Pages 629-643, ISSN 0092-8674.

6. Lakhtakia, R. A Brief History of Breast Cancer: Part I: Surgical domination reinvented. // Sultan Qaboos University Medical Journal. 2014; 14(2): 166–169.

7. Prieto-García, E., Díaz-García, C.V., García-Ruiz, I. et al. Epithelial-to-mesenchymal transition in tumor progression. Med Oncol J. (2017) 34: 122.

8. Tabar, L., Dean, P.B. Thirty years of experience with mammography screening: a new approach to the diagnosis and treatment of breast cancer. // Breast Cancer Research : BCR. 2008;10(Suppl 4): S3.

9. Tabar, L., Tony Chen, H., Amy Yen, M. F., Tot, T., Tung, T., Chen, L., Chiu, Y., Duffy, S.W. and Smith, R.A. (2004), Mammographic tumor features can predict long-term outcomes reliably in women with 1–14 mm invasive breast carcinoma. // Cancer, 101: 1745-1759.

For citation

Puchkova O.S., Sinicyn V.E., Bogomazova S.Yu., Mershina E.A., Shirokij V.P., Bazhenova D.A., Nenajdenko E.V. Correlation of the size, histology subtype of breast cancer at the time of detection, and the tumor grade. Bulletin of Pirogov National Medical & Surgical Center. 2019;14(1):45-48. (In Russ.) https://doi.org/10.25881/BPNMSC.2019.24.68.009