CLINICAL AND BIOLOGICAL MODEL FOR EVALUATION OF THE EFFECTIVENESS OF SYSTEMIC THERAPY FOR BREAST CANCER
PDF (Русский)

Keywords

BREAST CANCER
RADIOLOGICAL DIAGNOSTIC METHODS
BIOLOGICAL SUBTYPES
SYSTEMIC TREATMENT

How to Cite

Semiglazov, V., Trufanova, Y., Krzhivitskiy, P., Belyaev, A., Kondakova, A., Yereshchenko, S., Zhiltsova, Y., Mishchenko, A., Bashlyk, V., Kudaybergenova, A., Klimenko, V., Artemeva, A., Semiglazov, V., Busko, Y., Komyakhov, A., Semiglazova, T., Dashyan, G., Krivorotko, P., & Tseluyko, A. (2018). CLINICAL AND BIOLOGICAL MODEL FOR EVALUATION OF THE EFFECTIVENESS OF SYSTEMIC THERAPY FOR BREAST CANCER. Voprosy Onkologii, 64(3), 289–297. https://doi.org/10.37469/0507-3758-2018-64-3-289-297

Abstract

Purpose: To create a unified system of accelerated clinical trials of new drugs and regimens for breast cancer (BC).

Materials and methods: The study included 1214 patients with BC of different stages (cT1N1, cT2N1-2, cT2-3N0-2, cT2-3N0-1, cT4N0M0). According to trepan biopsy data and immunohistochemical examination (IHC) expression of ER, PR, HER2, and Ki67 was determined. The expression TUBBßIII, TOP2a, analyzes on the BRCA1/2 mutation was studied. The clinical response to neoadjuvant treatment was determined using the physical method, ultrasonography-elas-tography, mammography, contrast magnetic resonance imaging (MRI) and single-photon emission computer mammotography (SPECT-CT).

Results: The correlation index of complete responses (cCR) and total pathomorphological responses (pCR) according to MRI was 0.80, according to ultrasound - 0.61, mammography - 0.60, palpation - 0.57. The low level of amplification of the TUBßIII mRNA gene with a high level of amplification of the TOP2-a gene is a predictor of the achievement of pCR. The inclusion of a neoadjuvant treatment of triply-negative BC carboplatin in addition to paclitaxel or eribulin increases the frequency of reaching pCR (ypT0/is(yp)N0) from 20.3% to 47%.

https://doi.org/10.37469/0507-3758-2018-64-3-289-297
PDF (Русский)

References

Давыдов М.И. Статистика злокачественных новообразований в России и странах СНГ в 2012 г. - Москва: Издательская группа РОНЦ, 2014. - 226 с.

Семиглазов В.Ф., Семиглазов В.В. Рак молочной железы: биология, местное и системное лечение. - Москва, СИМК, 2014. - 352 с.

Семиглазов В.Ф., Криворотько П.В., Семиглазова Т.Ю. и др. Практические рекомендации по лечению рака молочной железы. - Мегаполис, М., 2017. - 168 с.

Семиглазов В.Ф., Криворотько П.В., Семиглазов В.В., Дашян Г.А., Палтуев РМ. Рекомендации для врачей по ведению пациентов с раком молочной железы. Специализированное издание, предназначенное для медицинских и фармацевтических работников. - Москва, 2017.

Семиглазов В.Ф. Лечение рака молочной железы: клинико-биологическое обоснование / Под ред. проф. В.Ф. Семиглазова, д.м.н. В.В. Семиглазова. - Москва: СИМК, 2017. - 272 с.

Goldhirsch A., Winer E.P., Coates A.S., et al. Personalizing the treatment of women with early breast cancer: highlights of the st Gallen International expert Consensus on the Primary Therapy of early Breast Cancer 2013 // Ann oncol. - 2013. - Vol. 24. - P 2206-2223.

Chia S.K. Neoadjuvant and Adjuvant therapy for HER2 Positive Disease // Clin. oncol. - 2015. - Vol. 35. - P 41-48.

Vas-Luis I., Ottesen R.A., Hughes M.E. et al. outcomes by tumor subtype and treatment pattern in women with small node negative breast cancer: a multi-institutional study // J. Clin. oncol. - 2014. - Vol. 32. - P. 2142-2150.

Bianchini G., Pusztai L., Pienkowski t. et al. Immune modulation of pathologic complete response after neoadjuvant HER2-directed therapies in the Neosphere trial // Ann. oncol. - 2015. - Vol. 26 (12). - P. 2429-2436.

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

© АННМО «Вопросы онкологии», Copyright (c) 2018