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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">uzspbgmu</journal-id><journal-title-group><journal-title xml:lang="ru">Учёные записки Первого Санкт-Петербургского государственного медицинского университета имени академика И. П. Павлова</journal-title><trans-title-group xml:lang="en"><trans-title>The Scientific Notes of the Pavlov University</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1607-4181</issn><issn pub-type="epub">2541-8807</issn><publisher><publisher-name>Academician I.P. Pavlov First St. Petersburg State Medical University</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.24884/1607-4181-2026-33-2-56-66</article-id><article-id custom-type="elpub" pub-id-type="custom">uzspbgmu-1221</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ РАБОТЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL PAPERS</subject></subj-group></article-categories><title-group><article-title>Оценка компонентов и площади ложа опухоли при полном патоморфологическом ответе после неоадъювантной химиотерапии у пациенток с ранним раком молочной железы: сравнение вакуум-ассистированной биопсии и стандартного хирургического материала</article-title><trans-title-group xml:lang="en"><trans-title>Evaluation of tumor bed area and components in patients with early breast cancer achieved pathological complete response after neoadjuvant chemotherapy: comparison of vacuum-assisted biopsy and standard surgical specimens</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0000-7635-2502</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Михаськова</surname><given-names>Н. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Mikhaskova</surname><given-names>N. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Михаськова Надежда Сергеевна, врач-ординатор патологоанатомического отделения </p><p>197758, Санкт-Петербург, Ленинградская ул., д. 68 </p></bio><bio xml:lang="en"><p>Mikhaskova Nadezhda S., Resident Pathologist, Department of Pathological Anatomy </p><p>68, Leningradskaya str., Saint Petersburg, 197758 </p></bio><email xlink:type="simple">iodiosono@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2421-3284</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Амиров</surname><given-names>Н. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Amirov</surname><given-names>N. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Амиров Николай Сергеевич, кандидат медицинских наук, врач-онколог отделения опухолей молочной железы</p><p>197758, Санкт-Петербург, Ленинградская ул., д. 68 </p></bio><bio xml:lang="en"><p>Amirov Nikolay S., Cand. of Sci. (Med.), Oncologist, Department of Breast Tumors</p><p>68, Leningradskaya str., Saint Petersburg, 197758 </p></bio><email xlink:type="simple">amirovn17@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0009-1460-4108</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Смутин</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Smutin</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Смутин Даниил Валерьевич, инженер института прикладных компьютерных наук</p><p>197101, Санкт-Петербург, Кронверкский проспект, д. 49, лит. А </p></bio><bio xml:lang="en"><p>Smutin Daniil V., Engineer, Institute of Applied Computer Science </p><p>49, lit. A, Kronverksky pr., Saint Petersburg, 197101 </p></bio><email xlink:type="simple">smutin@sut.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4898-9159</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Криворотько</surname><given-names>П. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Krivorotko</surname><given-names>P. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Криворотько Петр Владимирович, доктор медицинских наук, профессор, зав. отделением – врач-онколог отделения опухолей молочной железы, зав. отделением – врач-пластический хирург отделения онкологии и реконструктивно-пластической хирургии, ведущий научный сотрудник научного отделения опухолей молочной железы</p><p>197758, Санкт-Петербург, Ленинградская ул., д. 68 </p></bio><bio xml:lang="en"><p>Krivorotko Petr V., Dr. of Sci. (Med.), Professor, Oncologist, Head of the Department of Breast Tumors; Plastic Surgeon, Head of the Department of Oncology and Reconstructive-Plastic Surgery; Leading Research Fellow, Scientific Department of Breast Tumors</p><p>68, Leningradskaya str., Saint Petersburg, 197758 </p></bio><email xlink:type="simple">dr.krivorotko@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7797-088X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кудайбергенова</surname><given-names>А. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Kudaibergenova</surname><given-names>A. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кудайбергенова Асель Галимовна, кандидат медицинских наук, врач-патологоанатом патологоанатомического отделения, старший научный сотрудник научной лаборатории морфологии опухолей</p><p>197758, Санкт-Петербург, Ленинградская ул., д. 68 </p></bio><bio xml:lang="en"><p>Kudaibergenova Asel G., Cand. of Sci. (Med.), Pathologist, Department of Pathological Anatomy; Senior Research Fellow, Laboratory of Tumor Morphology</p><p>68, Leningradskaya str., Saint Petersburg, 197758 </p></bio><email xlink:type="simple">asel1972@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Национальный медицинский исследовательский центр онкологии имени Н. Н. Петрова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>N. N. Petrov National Medical Research Center of Oncology</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Национальный исследовательский университет информационных технологий, механики и оптики (Университет ИТМО)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Research University of Information Technologies, Mechanics and Optics (ITMO University)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>09</day><month>10</month><year>2026</year></pub-date><volume>33</volume><issue>2</issue><fpage>56</fpage><lpage>66</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Михаськова Н.С., Амиров Н.С., Смутин Д.В., Криворотько П.В., Кудайбергенова А.Г., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Михаськова Н.С., Амиров Н.С., Смутин Д.В., Криворотько П.В., Кудайбергенова А.Г.</copyright-holder><copyright-holder xml:lang="en">Mikhaskova N.S., Amirov N.S., Smutin D.V., Krivorotko P.V., Kudaibergenova A.G.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.sci-notes.ru/jour/article/view/1221">https://www.sci-notes.ru/jour/article/view/1221</self-uri><abstract><sec><title>Введение</title><p>Введение. В настоящее время наблюдается устойчивый тренд к деэскалации хирургического лечения при раке молочной железы (РМЖ), ключевую роль в которой играют возможности современной неоадъювантной химиотерапии (НАХТ), повышающей частоту клинического (cCR) и патоморфологического ответа (pCR). Нередко при выборе хирургического вмешательства при достижении полного регресса предпочтение отдается в пользу миниинвазивных методик, таких как вакуум-ассистированная биопсия (ВАБ). Патоморфологическая оценка ответа опухоли на НАХТ требует стандартизированного подхода и включает использование специальных шкал, одной из которых является расчет индекса остаточной опухолевой нагрузки (RCB). Линейные размеры ложа опухоли, которые являются одним из важных компонентов формулы, невозможно оценить на фрагментированном материале ВАБ.</p></sec><sec><title>Цель</title><p>Цель. Изучить возможность оценки площади ложа опухоли на материале ВАБ в сравнении со стандартным хирургическим вмешательством у пациенток с ранним РМЖ, достигших полного клинического и патоморфологического ответа после НАХТ.</p></sec><sec><title>Методы и материалы</title><p>Методы и материалы. В исследование включено 57 пациенток с РМЖ сT1-2N0-1M0, получавших НАХТ и достигших pCR. ВАБ была выполнена 21 пациентке, 36 получили стандартное хирургическое лечение (мастэктомия (МЭ)/ органосохранная операция (ОСО)). Гистологический материал оцифровывался с помощью сканера микропрепаратов 3D HISTECH PANORAMIC 1000, проводилась ручная разметка площади ложа опухоли различными методами.</p></sec><sec><title>Результаты</title><p>Результаты. Средний возраст пациенток составил 48,79 лет (27–68), в группе ВАБ – 49,19 лет (35–68), в группе стандартного вмешательства – 48,56 лет (27–68). Медиана площади ложа опухоли с терминальными протоково-дольковыми единицами (ТПДЕ) в ВАБ составила 175,24 (124,73–309,69), в группе стандартного вмешательства – 151,83 (85,66–282,67). Медиана площади ложа опухоли без ТПДЕ в ВАБ составила 170,07 (123,75–262,69), в группе стандартного вмешательства –129,86 (79,39–264,08). Различия между группами при сравнении площади ложа опухоли с ТПДЕ и без не достигли статистической значимости (критерий Манна – Уитни U=448,0, p=0,2503 и U= 450,0, p=0,2369). Медиана ТПДЕ/мм2 составила 0,274 (0,150–0,452), для группы ВAБ 0,265 (0,177–0,461), для группы стандартного вмешательства 0,278 (0,150–0,365). Статистически значимой разницы в плотности ТПДЕ/мм2 между группами не выявлено (критерий Манна – Уитни U=455,5, p=0,203). При анализе плотности ТПДЕ относительно возраста отмечается нисходящий линейный тренд. Средняя относительная доля ТПДЕ в образцах составила 6,67 % (0,00–28,40). Для группы ВАБ средняя относительная доля составила 6,34 % (0,79–19,94), для группы стандартного вмешательства 6,87 % (0,00–28,40).</p></sec><sec><title>Выводы</title><p>Выводы. Объем гистологического материала, получаемого при ВАБ, является сопоставимым с хирургическими образцами в контексте оценки площади ложа опухоли. Средняя доля ТПДЕ в образцах составляет около 6 %, однако в частных случаях в ложе опухоли сохраняются остаточные структуры аденоза, что может увеличивать среднюю долю ТПДЕ до 29 %.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Currently, there is a consistent trend toward de-escalation of surgical treatment in breast cancer (BC), largely driven by advances in modern neoadjuvant chemotherapy (NACT), which increase the rates of clinical (cCR) and pathological complete response (pCR). When complete regression is achieved, minimally invasive approaches such as vacuum-assisted biopsy (VAB) are often preferred over conventional surgery. Pathomorphological assessment of tumor response to NACT requires a standardized approach and often involves specialized grading systems, one of which is the Residual Cancer Burden (RCB) index. However, one of the key components of the RCB formula – the linear dimensions of the tumor bed – cannot be accurately determined from fragmented VAB specimens.</p><p>The objective was to evaluate the feasibility of measuring the tumor bed area in VAB specimens compared to standard surgical samples in patients with early-stage breast cancer who achieved both clinical and pathological complete responses following NACT.</p></sec><sec><title>Methods and materials</title><p>Methods and materials. The study included 57 patients with breast cancer cT1–2N0–1M0 who received NACT and achieved pCR. VAB was performed in 21 patients, while 36 underwent standard surgical treatment (mastectomy or breast-conserving surgery). Histological specimens were digitized using a 3D HISTECH PANORAMIC 1000 slide scanner, and manual annotation of tumor bed areas was performed using various methods.</p></sec><sec><title>Results</title><p>Results. The mean age of the patients was 48.79 years (range 27–68): 49.19 years (35–68) in the VAB group and 48.56 years (27–68) in the standard surgery group.The median tumor bed area with terminal ductal-lobular units (TDLU) in the VAB group was 175.24 mm2 (124.73–309.69), and 151.83 mm2 (85.66–282.67) in the standard surgery group. The median tumor bed area without TDLU was 170.07 mm2 (123.75–262.69) for VAB and 129.86 mm2 (79.39–264.08) for standard surgery. Differences between the groups were not statistically significant (Mann–Whitney U=448.0, p=0.2503, and U=450.0, p=0.2369, respectively). The median TDLU density was 0.274/mm2 (0.150–0.452): 0.265/mm2 (0.177–0.461) in the VAB group and 0.278/mm2 (0.150–0.365) in the surgery group. No statistically significant differences in TDLU density were observed (Mann–Whitney U=455.5, p=0.203). A downward linear trend in TDLU density was observed with increasing age. The mean relative proportion of TDLU in the samples was 6.67 % (0.00–28.40): 6.34 % (0.79–19.94) in the VAB group and 6.87 % (0.00–28.40) in the standard surgery group.</p></sec><sec><title>Conclusions</title><p>Conclusions. The volume of histological material obtained via vacuum-assisted biopsy is comparable to that from surgical specimens in the context of tumor bed area assessment. The average proportion of TDLU in samples is approximately 6 %; however, in some cases, residual adenosis structures may persist within the tumor bed, increasing the TDLU proportion to as much as 29 %.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>рак молочной железы</kwd><kwd>ВАБ</kwd><kwd>ложе опухоли</kwd><kwd>RCB</kwd><kwd>pCR</kwd><kwd>НАХТ</kwd></kwd-group><kwd-group xml:lang="en"><kwd>breast cancer</kwd><kwd>VAB</kwd><kwd>tumor bed</kwd><kwd>RCB</kwd><kwd>pCR</kwd><kwd>NACT</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Cortazar P., Zhang L., Untch M. et al. Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis // The Lancet. – 2014. – Vol. 9938, № 384. – P. 164–172. https://doi.org/10.1016/S0140-6736(13)62422-8.</mixed-citation><mixed-citation xml:lang="en">Cortazar P., Zhang L., Untch M. et al. Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis // The Lancet. 2014; 9938(384):164–172. https://doi.org/10.1016/S0140-6736(13)62422-8.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">van Mackelenbergh M. T., Loibl S., Untch M. et al. Pathologic Complete Response and Individual Patient Prognosis After Neoadjuvant Chemotherapy Plus Anti-Human Epidermal Growth Factor Receptor 2 Therapy of Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer // Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology. – 2023. – Vol. 16, № 41. – P. 2998–3008. https://doi.org/10.1200/jco.22.02241.</mixed-citation><mixed-citation xml:lang="en">van Mackelenbergh M. T., Loibl S., Untch M. et al. Pathologic Complete Response and Individual Patient Prognosis After Neoadjuvant Chemotherapy Plus Anti-Human Epidermal Growth Factor Receptor 2 Therapy of Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer // Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology. 2023;16(41):2998– 3008. https://doi.org/10.1200/jco.22.02241.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Buzdar A. U., Valero V., Ibrahim N. K. et al. Neoadjuvant therapy with paclitaxel followed by 5-fluorouracil, epirubicin, and cyclophosphamide chemotherapy and concurrent trastuzumab in human epidermal growth factor receptor 2-positive operable breast cancer: an update of the initial randomized study population and data of additional patients treated with the same regimen // Clinical Cancer Research: An Official Journal of the American Association for Cancer Research. – 2007. – Vol. 1, № 13. – P. 228–233. https://doi.org/10.1158/1078-0432.CCR-06-1345.</mixed-citation><mixed-citation xml:lang="en">Buzdar A. U., Valero V., Ibrahim N. K. et al. Neoadjuvant therapy with paclitaxel followed by 5-fluorouracil, epirubicin, and cyclophosphamide chemotherapy and concurrent trastuzumab in human epidermal growth factor receptor 2-positive operable breast cancer: an update of the initial randomized study population and data of additional patients treated with the same regimen // Clinical Cancer Research: An Official Journal of the American Association for Cancer Research. 2007;1(13):228–233. https://doi.org/10.1158/1078-0432.CCR-06-1345.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Green M. C., Buzdar A. U., Smith T. et al. Weekly Paclitaxel Improves Pathologic Complete Remission in Operable Breast Cancer When Compared With Paclitaxel Once Every 3 Weeks // Journal of Clinical Oncology. – 2005. – Vol. 25, № 23. – P. 5983–5992. https://doi.org/10.1200/JCO.2005.06.232.</mixed-citation><mixed-citation xml:lang="en">Green M. C., Buzdar A. U., Smith T. et al. Weekly Paclitaxel Improves Pathologic Complete Remission in Operable Breast Cancer When Compared With Paclitaxel Once Every 3 Weeks // Journal of Clinical Oncology. 2005;25(23):5983– 5992. https://doi.org/10.1200/JCO.2005.06.232.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Hortobagyi G. N., Buzdar A. U., Theriault R. L. et al. Randomized Trial of High-Dose Chemotherapy and Blood Cell Autografts for High-Risk Primary Breast Carcinoma // JNCI: Journal of the National Cancer Institute. – 2000. – Vol. 3, № 92. – P. 225–233. https://doi.org/10.1093/jnci/92.3.225.</mixed-citation><mixed-citation xml:lang="en">Hortobagyi G. N., Buzdar A. U., Theriault R. L. et al. Randomized Trial of High-Dose Chemotherapy and Blood Cell Autografts for High-Risk Primary Breast Carcinoma // JNCI: Journal of the National Cancer Institute. 2000;3(92): 225–233. https://doi.org/10.1093/jnci/92.3.225.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Symmans W. F., Peintinger F., Hatzis С. et al. Measurement of Residual Breast Cancer Burden to Predict Survival After Neoadjuvant Chemotherapy // Journal of Clinical Oncology. – 2007. – Vol. 28, № 25. – P. 4414–4422. https://doi.org/10.1200/JCO.2007.10.6823.</mixed-citation><mixed-citation xml:lang="en">Symmans W. F., Peintinger F., Hatzis С. et al. Measurement of Residual Breast Cancer Burden to Predict Survival After Neoadjuvant Chemotherapy // Journal of Clinical Oncology. 2007;28(25):4414–4422. https://doi.org/10.1200/JCO.2007.10.6823.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Криворотько П. В., Амиров Н. С., Артемьева А. С. и др. Оценка результатов лечения в зависимости от различных видов локального воздействия у пациентов с диагнозом рак молочной железы с полным патоморфологическим ответом после неоадъювантной системной терапии // Вопросы онкологии. – 2024. – Т. 2, № 70. – C. 330–339.</mixed-citation><mixed-citation xml:lang="en">Krivorotko P. V., Amirov N. S., Artemyeva A. S. et al. Treatment Outcomes Evaluation in Breast Cancer Patients with a Pathological Complete Response after Neoadjuvant Systemic Therapy Depending on Different Types of Local Treatment // Oncology questions. 2024;2(70):330–339. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Kuerer H. M., Rauch G. M., Krishnamurthy S. et al. A Clinical Feasibility Trial for Identification of Exceptional Responders in Whom Breast Cancer Surgery Can Be Eliminated Following Neoadjuvant Systemic Therapy // Annals of Surgery. – 2018. – Vol. 5, № 267. – P. 946–951. https://doi.org/10.1016/S1470-2045(22)00613-1.</mixed-citation><mixed-citation xml:lang="en">Kuerer H. M., Rauch G. M., Krishnamurthy S. et al. A Clinical Feasibility Trial for Identification of Exceptional Responders in Whom Breast Cancer Surgery Can Be Eliminated Following Neoadjuvant Systemic Therapy // Annals of Surgery. 2018;5(267):946–951. https://doi.org/10.1016/S1470-2045(22)00613-1.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Kuerer H. M., Smith B. D., Krishnamurthy S. et al. Eliminating breast surgery for invasive breast cancer in exceptional responders to neoadjuvant systemic therapy: a multicentre, single-arm, phase 2 trial // The Lancet Oncology. – 2022. – Vol. 12, № 23. – P. 1517–1524. https://doi.org/10.1097/SLA.0000000000002313.</mixed-citation><mixed-citation xml:lang="en">Kuerer H. M., Smith B. D., Krishnamurthy S. et al. Eliminating breast surgery for invasive breast cancer in exceptional responders to neoadjuvant systemic therapy: a multicentre, single-arm, phase 2 trial // The Lancet Oncology. 2022;12(23):1517–1524. https://doi.org/10.1097/SLA.0000000000002313.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Amin M. B., Greene F. L., Edge S. B. et al. AJCC Cancer Staging Manual / Mahul B. Amin, Stephen B. Edge, Frederick L. Greene, David R. Byrd., 8-е изд., Springer, 2017.</mixed-citation><mixed-citation xml:lang="en">Amin M. B., Greene F. L., Edge S. B. et al. AJCC Cancer Staging Manual / Mahul B. Amin, Stephen B. Edge, Frederick L. Greene, David R. Byrd., 8th ed. Springer, 2017.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Ogston K. N., Miller I. D., Payne S. et al. A new histological grading system to assess response of breast cancers to primary chemotherapy: prognostic significance and survival // The Breast. – 2003. – Vol. 5, № 12. – P. 320–327. https://doi.org/10.1016/S0960-9776(03)00106-1.</mixed-citation><mixed-citation xml:lang="en">Ogston K. N., Miller I. D., Payne S. et al. A new histological grading system to assess response of breast cancers to primary chemotherapy: prognostic significance and survival // The Breast. 2003;5(12):320–327. https://doi.org/10.1016/S0960-9776(03)00106-1.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Corben A. D., Abi-Raad R., Popa I. et al. Pathologic Response and Long-Term Follow-up in Breast Cancer Patients Treated With Neoadjuvant Chemotherapy: A Comparison Between Classifications and Their Practical Application // Archives of Pathology &amp; Laboratory Medicine. – 2013. – Vol. 8, № 137. – P. 1074–1082. https://doi.org/10.5858/arpa.2012-0290-OA.</mixed-citation><mixed-citation xml:lang="en">Corben A. D., Abi-Raad R., Popa I. et al. Pathologic Response and Long-Term Follow-up in Breast Cancer Patients Treated With Neoadjuvant Chemotherapy: A Comparison Between Classifications and Their Practical Application // Archives of Pathology &amp; Laboratory Medicine. 2013;8(137):1074–1082. https://doi.org/10.5858/arpa.2012-0290-OA.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Lee H. J., Park I. A., Song I. H. et al. Comparison of Pathologic Response Evaluation Systems after Anthracycline with/without Taxane-Based Neoadjuvant Chemotherapy among Different Subtypes of Breast Cancers // PLOS ONE. – 2015. – Vol. 9, № 10. – P. e0137885. https://doi.org/10.1371/journal.pone.0137885.</mixed-citation><mixed-citation xml:lang="en">Lee H. J., Park I. A., Song I. H. et al. Comparison of Pathologic Response Evaluation Systems after Anthracycline with/without Taxane-Based Neoadjuvant Chemotherapy among Different Subtypes of Breast Cancers // PLOS ONE. 2015;9(10):e0137885. https://doi.org/10.1371/journal.pone.0137885.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang G. C., Zhang Y. F., Xu F. P. et al.Axillary lymph node status, adjusted for pathologic complete response in breast and axilla after neoadjuvant chemotherapy, predicts differential disease-free survival in breast cancer // Current Oncology. – 2013. – Vol. 3, № 20. – P. e180–e192. https://doi.org/10.3747/co.20.1294.</mixed-citation><mixed-citation xml:lang="en">Zhang G. C., Zhang Y. F., Xu F. P. et al. Axillary lymph node status, adjusted for pathologic complete response in breast and axilla after neoadjuvant chemotherapy, predicts differential disease-free survival in breast cancer // Current Oncology. 2013;3(20):e180–e192. https://doi.org/10.3747/co.20.1294.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Park K. U., Somerfield M. R., Anne N. et al. Sentinel Lymph Node Biopsy in Early-Stage Breast Cancer: ASCO Guideline Update // Journal of Clinical Oncology. – 2025. – Vol. 14, № 43. – P. 1720–1741. https://doi.org/10.1200/JCO-25-00099.</mixed-citation><mixed-citation xml:lang="en">Park K. U., Somerfield M. R., Anne N. et al. Sentinel Lymph Node Biopsy in Early-Stage Breast Cancer: ASCO Guideline Update // Journal of Clinical Oncology. 2025;14(43):1720–1741. https://doi.org/10.1200/JCO-25-00099.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Detailed Pathology Methods for Using Residual Cancer Burden. URL: https://www.mdanderson.org/content/dam/mdanderson/documents/for-physicians/clinical-calculators/PLM_protocol_RCB_calculators_BRO.pdf (accessed: 09.11.2025).</mixed-citation><mixed-citation xml:lang="en">Detailed Pathology Methods for Using Residual Cancer Burden. URL: https://www.mdanderson.org/content/dam/mdanderson/documents/for-physicians/clinical-calculators/PLM_protocol_RCB_calculators_BRO.pdf (accessed: 09.11.2025).</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Heil J., Pfob A., Sinn H. P. et al. Diagnosing Pathologic Complete Response in the Breast After Neoadjuvant Systemic Treatment of Breast Cancer Patients by Minimal Invasive Biopsy: Oral Presentation at the San Antonio Breast Cancer Symposium on Friday, December 13, 2019, Program Number GS5-03 // Annals of surgery. – 2022. – Vol. 3, № 275.</mixed-citation><mixed-citation xml:lang="en">Heil J., Pfob A., Sinn H. P. et al. Diagnosing Pathologic Complete Response in the Breast After Neoadjuvant Systemic Treatment of Breast Cancer Patients by Minimal Invasive Biopsy: Oral Presentation at the San Antonio Breast Cancer Symposium on Friday, December 13, 2019, Program Number GS5-03 // Annals of surgery. 2022;3(275).</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Tasoulis M. K., Lee H. B., Yang W. et al. Accuracy of Post–Neoadjuvant Chemotherapy Image-Guided Breast Biopsy to Predict Residual Cancer // JAMA Surgery. – 2020. – Vol. 12, № 155. – P. e204103. https://doi.org/10.1001/jamasurg.2020.4103.</mixed-citation><mixed-citation xml:lang="en">Tasoulis M. K., Lee H. B., Yang W. et al. Accuracy of Post–Neoadjuvant Chemotherapy Image-Guided Breast Biopsy to Predict Residual Cancer // JAMA Surgery. 2020;12(155):e204103. https://doi.org/10.1001/jamasurg.2020.4103.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Амиров Н. С., Артемьева А. С., Криворотько П. В. и др. Патоморфологическое исследование материала, полученного при использовании вакуум-ассистированной биопсии у пациентов с диагнозом рак молочной железы после неоадъювантной системной терапии // Ученые записки СПбГМУ им. И. П. Павлова. – 2024. – Т. 2, № 31. – C. 28–43. https://doi.org/10.24884/1607-4181-2024-31-2-28-43.</mixed-citation><mixed-citation xml:lang="en">Amirov N. S., Artemyeva A. S., Krivorotko P. V. et al. Pathomorphological examination of specimen after vacuum-assisted biopsy in patients with breast cancer after neoadjuvant systemic therapy // The Scientific Notes of the Pavlov University. 2024;31(2):28‒43. (In Russ.). https://doi.org/10.24884/1607-4181-2024-31-2-28-43.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Protocol for the Examination of Resection Specimens from Patients with Invasive Carcinoma of the Breast, Version: 4.10.0.0, 2024, College of American Pathologists (CAP).</mixed-citation><mixed-citation xml:lang="en">Protocol for the Examination of Resection Specimens from Patients with Invasive Carcinoma of the Breast, Version: 4.10.0.0, 2024, College of American Pathologists (CAP).</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Invasive Carcinoma of the Breast in the Setting of Neoadjuvant Therapy // 2025, ICCR URL: https://www.iccr-cancer.org/datasets/published-datasets/breast/breast-neoadjuvant-therapy/ (дата обращения: 23.09.2025).</mixed-citation><mixed-citation xml:lang="en">Invasive Carcinoma of the Breast in the Setting of Neoadjuvant Therapy // 2025, ICCR URL: https://www.iccr-cancer.org/datasets/published-datasets/breast/breast-neoadjuvant-therapy/ (accessed: 23.09.2025).</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Loibl S., O’Shaughnessy J., Untch M. et al. Addition of the PARP inhibitor veliparib plus carboplatin or carboplatin alone to standard neoadjuvant chemotherapy in triple-negative breast cancer (BrighTNess): a randomised, phase 3 trial // The Lancet. Oncology. ‒ 2018. ‒ № 4 (19). ‒ C. 497–509. https://doi.org/10.1016/S1470-2045(18)30111-6.</mixed-citation><mixed-citation xml:lang="en">Loibl S., O’Shaughnessy J., Untch M. et al. Addition of the PARP inhibitor veliparib plus carboplatin or carboplatin alone to standard neoadjuvant chemotherapy in triple-negative breast cancer (BrighTNess): a randomised, phase 3 trial // The Lancet. Oncology. 2018;4(19):497–509. https://doi.org/10.1016/S1470-2045(18)30111-6.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Pérez-García J. M., Gebhart G., Ruiz Borrego M. et al. Chemotherapy de-escalation using an 18F-FDG-PET-based pathological response-adapted strategy in patients with HER2-positive early breast cancer (PHERGain): a multi-centre, randomised, open-label, non-comparative, phase 2 trial // The Lancet. Oncology. – 2021. – Vol. 6, № 22. – P. 858–871. https://doi.org/10.1016/S1470-2045(21)00122-4.</mixed-citation><mixed-citation xml:lang="en">Pérez-García J. M., Gebhart G., Ruiz Borrego M. et al. Chemotherapy de-escalation using an 18F-FDG-PETbased pathological response-adapted strategy in patients with HER2-positive early breast cancer (PHERGain): a multicentre, randomised, open-label, non-comparative, phase 2 trial // The Lancet. Oncology. 2021;6(22):858–871. https://doi.org/10.1016/S1470-2045(21)00122-4.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Pusztai L., Denkert C., O’Shaughnessy J. et al. Eventfree survival by residual cancer burden with pembrolizumab in early-stage TNBC: exploratory analysis from KEYNOTE-522 // Annals of Oncology: Official Journal of the European Society for Medical Oncology. – 2024. – Vol. 5, № 35. – P. 429–436. https://doi.org/10.1016/j.annonc.2024.02.002.</mixed-citation><mixed-citation xml:lang="en">Pusztai L., Denkert C., O’Shaughnessy J. et al. Eventfree survival by residual cancer burden with pembrolizumab in early-stage TNBC: exploratory analysis from KEYNOTE-522 // Annals of Oncology: Official Journal of the European Society for Medical Oncology. 2024;5(35):429–436. https://doi.org/10.1016/j.annonc.2024.02.002.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Башлык В. О., Семиглазов В. Ф., Кудайбергенова А. Г. и др. Оценка изменения морфологических и иммуногистохимических характеристик карцином молочной железы при проведении неоадъювантной системной терапии // Опухоли женской репродуктивной системы. – 2018. – Т. 14, № 1. – C. 12–19.</mixed-citation><mixed-citation xml:lang="en">Bashlyk V. О., Semiglazov V. F., Kudaybergenova A. G. et al. Evaluation of morphological and immunohistochemical changes of breast carcinomas after neoadjuvant systemic therapy // Tumors of female reproductive system. 2018;14(1):12‒19. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Koelbel V., Pfob A., Schaefgen B. et al. Vacuum-Assisted Breast Biopsy After Neoadjuvant Systemic Treatment for Reliable Exclusion of Residual Cancer in Breast Cancer Patients // Annals of Surgical Oncology. – 2022. – Vol. 28, № 2. – P. 1076–1084.</mixed-citation><mixed-citation xml:lang="en">Koelbel V., Pfob A., Schaefgen B. et al. Vacuum-Assisted Breast Biopsy After Neoadjuvant Systemic Treatment for Reliable Exclusion of Residual Cancer in Breast Cancer Patients // Annals of Surgical Oncology. 2022;28(2):1076–1084.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
