Vol 6, No 1 (2026)
NEW APPROACHES AND SUCCESSES IN TREATMENT OF ONCOLOGICAL PATIENTS AT THE CURRENT STAGE
Modern possibilities of drug therapy for early and locally advanced triple negative breast cancer
Abstract
Triple negative breast cancer remains the subtype of breast cancer with the highest rates of recurrence and mortality. Research in the field of tumor biology has led to identification of subgroups of patients with specific molecular features, which has led to the development and approval of many new targeted treatments for this disease.
This review considers current options for the treatment of locally advanced forms of breast cancer at the neoadjuvant stage – the use of carboplatin, targeted therapy with vascular endothelial growth factor inhibitors and immunotherapy. It discusses the practical problems and unanswered questions that arise in connection with the approval of neoadjuvant immunotherapy, and describes the approach used in the clinical practice to use various treatment options and the possibility of combining them to achieve the best early and long-term results.
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Long-term response to treatment of metastatic HER2-positive gastric cancer. Clinical case
Abstract
Metastatic gastric cancer remains a disease with unfavorable prognosis, median overall survival with standard chemotherapy is less than 1 year. In 15–20 % of patients, the tumor is characterized by HER2 hyperexpression/amplification which allows to use targeted therapy. Results of the ToGA trial showed that addition of trastuzumab to the 1st line chemotherapy in HER2-positive patients statistically significantly increased median overall survival to 16.0 months in the high expression (immunohistochemistry 3+) group, and this regimen remains the standard treatment in these patients in the 1st line.
A clinical case of a 46-year-old female patient with disseminated HER2-positive (immunohistochemistry 3+) stage IV (primary tumor, metastases in the liver, ovary, carcinomatosis) is presented. During 1st line therapy (XELOX + trastuzumab), partial and later complete regression of the tumor lesions was achieved. After 10 courses of induction therapy, supportive therapy with capecitabine and trastuzumab was started which has been going for more than 9 years with overall survival of 123 months and duration of complete response 116 months.
Results of the observation show the possibility of exceptionally long and deep response to chemotherapy and trastuzumab combination in individual patients with HER2-positive metastatic gastric cancer which emphasizes significant heterogeneity of this patient subgroup. Optimization of metastatic gastric cancer treatment requires further study aimed at identification of predictive biomarkers of response to anti-HER2 therapy.
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Sentinel lymph node biopsy for breast cancer restaging
Abstract
Aim. To study the role of SLNB in patients with primary operable breast cancer (T1–2N0/N0–1) in restaging depending on the involvement of regional lymph flow (N status).
Materials and methods. The retrospective study included 956 women with ductal/lobular stage I–IIB breast cancer. The median age was 54 [45; 63] years. According to the TNM clinical staging system, the patients predominantly had stage IA and IIA cancer. In 94 % of patients, no involvement of the SLN was detected. N+ status was registered in 6 % of patients. Histologically, breast cancer was predominantly represented by invasive ductal carcinoma in 87.5 % of the patients. Depending on the molecular subtype, luminal B HER2neu negative breast cancer was found in 38.2 % of the patients and luminal A subtype in 29.6 %. Moderately differentiated breast cancer was found in 63.5 % of the patients.
Results. Median follow-up of the patients was 70.6 [60.0; 82.0] months. Depending on the involvement of the SLN, the following sentinel lymph node biopsy showed the following results: in 77.5 % of the patients, cN0 was confirmed histologically (pN0); in 2.7 %, SLN involvement was staged both clinically and pathologically (cN1–pN1); in 2.8 %, de-escalation of staging was detected (cN1–pN0); and in 0.6 %, SLNB revealed larger volume of damage to the regional lymph collector (cN1–pN2–3). 20 % of the patients underwent neoadjuvant chemotherapy (NACT). Among patients with cN1, SLN involvement (pN1) was significantly more often detected histologically in the group after NACT, 6.8 % versus 1.7 % (p = 0.0001), respectively. In 2.8 % with cN1–pN0, NACT efficacy was significantly higher (12.1 % versus 0.5 %, p = 0.00001). Also, in 16.3 % of the patients, pN1 was significantly more common in the group without NACT (18.5 % versus 7.4 %, p = 0.0002).
Conclusion. Conducting SLNB restaged the involvement of the regional lymph collector of T1–2N0/N0–1 patients in 189 (19.8 %) cases. According to the results of SLNB, in 528 (55.2 %) patients with breast cancer, it was possible to refuse lymphadenectomy.
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Multidisciplinary approach to management of patients with hereditary spherocytosis. Clinical observation
Abstract
Hereditary spherocytosis (HS) is a hemolytic anemia developing due to genetically induced defect in the erythrocyte membrane causing change in its shape. According to the results of studies, defects in the associated membrane proteins are caused by key mutations in the SLC4A1, EPB42, SPTA1, SPTB and ANK1 genes. The same mutation in different parts of a gene can lead to different clinical manifestations, therefore the studies of correlations between genotype and phenotype are necessary. Absence of wide availability, 100 % sensitivity and specificity of the laboratory methods used, as well as familial medical history in some cases, in conjunction with non-conformance with the clinical picture can lead to errors in HS diagnosis. Therefore, multidisciplinary approach is necessary. Progress in molecular biology led to development of next-generation sequencing which can aid in identification of new gene variants, analysis of their structure and potential pathogenicity. This will allow to significantly improve diagnostics and apply personalized treatment of HS.
The article presents results of clinical and diagnostic observation of a 45-year-old female patient whose condition due to hemolytic crisis determined the necessity of using comprehensive approach to therapy on an urgent basis in conjunction with differential diagnostic search and identification of the cause of anemia.
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False positive PET-CT result after treatment of a patient with diffuse large B-cell lymphoma. Clinical case
Abstract
The use of 18F-fluorodeoxyglucose positron emission tomography (PET-СT) to determine the initial stage and assess response to treatment in aggressive lymphomas is considered the standard. Evaluation of bone marrow infiltration in PET-CT with 18F-fluorodeoxyglucose usually allows to distinguish normal regenerating bone marrow after chemotherapy by its characteristic absorption.
A 54-year-old patient was diagnosed with diffuse large B-cell lymphoma with focal lesions in the lymph nodes and bone marrow with osteodestruction of the lytic type. Therapy at the A.F. Tsyb Medical Radiological Research Center consisted of 6 cycles of R-EPOCH with intrathecal administration of drugs for the prevention of neuroleukemia (dexamethasone + cytarabine + methotrexate), completed in December 2022. On intermediate PET-CT after 2 cycles, the glycolysis intensity was completely normalized. During the observation in February 2023, PET-CT showed an increase in the level of metabolism in one of the foci of osteodestruction in the pelvic bones. A guided biopsy of the lesion in March 2023 was performed, morphological conclusion: absence of signs of diffuse large B-cell lymphoma, elements of hematopoiesis of the bone marrow. In June 2023, repeated PET-CT showed continuing increase in contrast accumulation in the previously identified foci. Trephine biopsy in July 2023 showed a picture of hematopoietic foci in the bone marrow, a sign of remission. PET-CT scan in December 2023 showed a decrease in the intensity of glycolysis in the foci in the pelvic bones confirming remission of the disease.
In the era of rituximab, false-positive PET-CT results are detected with greater frequency, therefore, their assessment and correct interpretation, as well as additional clarification using other available techniques, are necessary in modern clinical practice to choose tactics for further therapy.
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The role of thrombopoietin receptor agonists in reducing complications of chemotherapy-induced thrombocytopenia in patients with hematologic malignancies: review and single-center experience
Abstract
Background. Chemotherapy-induced thrombocytopenia (CIT) is one of the most common and clinically significant complications of anticancer therapy. It limits the ability to maintain planned chemotherapy dose intensity, increases the risk of hemorrhagic complications, and leads to a higher demand for platelet transfusions. Given the limited efficacy and availability of transfusion support, the development of pharmacological approaches for CIT management is of high clinical relevance. Thrombopoietin receptor agonists, including avatrombopag, represent a promising strategy in supportive cancer care.
Aim. To evaluate the efficacy and clinical relevance of prophylactic avatrombopag use in patients with chemotherapy-induced thrombocytopenia.
Materials and methods. This observational study included 9 patients (4 males and 5 females) with oncological diseases who developed thrombocytopenia < 100 × 109/L after a previous chemotherapy cycle. The median age was 52 years (range 27–68). Avatrombopag was administered prophylactically after completion of chemotherapy at a dose of 40 mg/day (20 mg twice daily) for 5 or 10 days, depending on the severity of thrombocytopenia. The following parameters were analyzed: nadir platelet count during the inter-cycle period, incidence of hemorrhagic events, requirement for platelet transfusions, and duration of delay of the subsequent chemotherapy cycle.
Results. During avatrombopag administration, the median nadir platelet count remained unchanged at 10 × 109/L; however, a marked increase up to 79 × 109/L was observed in some patients. The incidence of hemorrhagic complications decreased from 55 to 11 %. The median number of platelet transfusions was reduced from 3 to 2 units. A significant reduction in chemotherapy delays was observed, with the median delay decreasing from 11 to 0 days. No avatrombopag-related adverse events were reported.
Conclusion. Prophylactic use of avatrombopag in patients with chemotherapy-induced thrombocytopenia was associated with a reduced incidence of bleeding complications, decreased need for platelet transfusions, and fewer delays in subsequent chemotherapy cycles. Despite the limited sample size, these findings support the clinical value of avatrombopag as a supportive therapy and warrant further prospective studies.
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RARE CONGENITAL SURGICAL PATHOLOGIES: DIAGNOSTIC CHALLENGES AND TREATMENT SELECTION
Ectopic liver (hepatic choristoma) in clinical practice: literature review and clinical case
Abstract
Choristoma is a region of normally formed tissue located in an abnormal location. Ectopic liver is a rare clinical condition characterized by the presence of hepatic tissue outside the anatomical and topographical location of the organ. Despite its low incidence, this condition requires special attention due to challenges of diagnosis and selection of the optimal treatment approach.
The article presents a clinical case of successful diagnosis and treatment of a patient with pain syndrome in the upper abdominal cavity caused by inflammation of an accessory liver lobe.
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THEORETICAL ASPECTS AND BASIC RESEARCH IN ONCOLOGY IN THE CURRENT AGE
Epidemiological and clinical features of multiple myeloma in Russia: results of a multicenter prospective study
Abstract
Background. Epidemiological studies aggregating data on newly diagnosed multiple myeloma (MM) from real-world clinical practice allow to analyze various clinical and laboratory parameters characterizing general trends in MM diagnosis, treatment outcomes, and life expectancy.
Aim. To determine overall survival rates in patients with newly diagnosed MM and to examine factors influencing survival in a population-based study.
Materials and methods. A total of 3,184 patients with a newly diagnosed MM from 40 regions of Russia were enrolled in a multicenter prospective study from January 2, 2015, to October 4, 2018. Complete registration of newly diagnosed cases was conducted at each of the 44 participating centers. Information on clinical and laboratory parameters, antitumor therapy regimens administered to patients, including autologous transplantation, was analyzed.
Results. The median age of MM patients in Russia was 63 years. It was shown that 39 % of the patients belonged to the older age group 66–90 years, and the percentage of patients under 55 years was 22 %. Only 9 % of patients underwent bone marrow cytogenetic testing. The proportion of patients with kidney damage was 26 %, while 5 % of patients were dialysis dependent. It was shown that 78 % of patients were diagnosed with stage 3 according to Durie–Salmon system, and in 52 % of cases, stage III according to International Staging System was diagnosed. Induction therapy included the use of bortezomib in 94 % of cases, the VCD regimen (bortezomib + dexamethasone + cyclophosphamide) was mainly used, lenalidomide was prescribed extremely rarely – in 1 % of cases. The proportion of patients under 65 years of age who received at least one autologous hematopoietic stem cell transplant was only 18 %. With autologous hematopoietic stem cell transplantation, the median overall survival was 107 months, and in the case of maintenance therapy with lenalidomide, it increased to 129 months. Five-year overall survival of the entire group of patients was 40 %. In a multivariate analysis, independent predictors of worse overall survival were Durie–Salmon stage III, substage B, profound anemia (hemoglobin ≤80 g/L), albumin ≤30 g/L, and hypercalcemia (≥3 mmol/L).
Conclusion. This multicenter prospective study of the epidemiological and clinical parameters of newly diagnosed multiple myeloma is unique in Russia in terms of coverage and follow-up duration (over 10 years). Analysis of treatment data for newly diagnosed multiple myeloma identified key issues in diagnosis and treatment.
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