


Vol 31, No 7 (2024)
- Year: 2024
- Articles: 19
- URL: https://journals.eco-vector.com/2073-4034/issue/view/10228
Reviews
Review of new clinical guidelines of the European Thyroid Association from the perspective of an ultrasound diagnostician. Our experience
Abstract
The article analyzes literature and own authors’ data on the use of the EU-TIRADS and Bethesda classification. Thyroid nodules are widespread in the population. Due to the unfavorable environmental situation, the spread of radiation methods for the treatment of tumors in other localizations, an increase in the incidence of thyroid cancer is noted. Having modern ultrasound machines with advanced auxiliary techniques (elastography, contrast-enhanced ultrasound, Doppler modes), the doctor often faces difficulties in interpreting the results of the study and making a decision on further patient management tactics. The TIRADS classification for thyroid nodules has been widely implemented abroad, according to which the management tactics for each group of patients are determined. In our country, doctors use various, sometimes contradictory, versions of the TIRADS classification. The purpose of the classification is to determine the risk of malignancy of the node and the choice of further tactics for patient management. According to statistics, the majority of thyroid nodes are benign. If malignancy is suspected, the patient undergo biopsy. Fine-needle aspiration biopsy (FNAB) with cytological examination is a fairly highly informative diagnostic method and allows for reliable interpretation of the ultrasound characteristics of thyroid nodes, as well as the choice of the necessary tactics for managing a specific patient. But like any interventional procedure, FNAB has complications and may have an uninformative result. The question arises about the need for a repeat biopsy and its timing. The article provides an overview of the latest clinical guidelines for the management of patients with thyroid nodules, published in August 2023 by the European Thyroid Association, from the point of view of an ultrasound diagnostic physician. It also presents data on 848 patients with thyroid nodules who underwent examination and treatment at the Chelyabinsk Regional Center for Oncology and Nuclear Medicine in 2023.



Cases of mycosis fungoides in children, adolescents and young adults (literature review)
Abstract
Mycosis fungoides is the most common form of primary cutaneous T-cell lymphomas diagnosed in adult patients aged 55–60 years and older. However, in foreign and domestic literature there are publications on cases of mycosis fungoides in children, adolescents and young adults. Before pathomorphological verification of the diagnosis, patients are usually followed-up for a long time by a dermatovenerologist with various chronic dermatoses.
This article provides literature review and description of own authors’ clinical observations confirming the development of the onset of the disease at a younger age, including in children and adolescents, which emphasizes the importance of cancer alertness in dermatovenerologists when conducting differential diagnostics of dermatoses of unknown genesis, as well as timely assignment of pathomorphological and immunohistochemical studies of skin biopsy.



Modern methods of thrombosis prevention and treatment in cancer patients with atrial fibrillation: focus on apixaban
Abstract
Recent studies confirm that endothelial dysfunction is an important pathogenetic mechanism in both atrial fibrillation and cancer-associated thromboses. It promotes inflammation, activation of coagulation and development of thrombosis, which requires the development of new therapeutic approaches to reduce the risk of thromboembolic complications (TEC) in such patients. The ongoing trials support the use of apixaban for the treatment of venous TEC in patients with active oncopathology in combination with atrial fibrillation, which confirms its efficacy and safety. This allows apixaban to be used both in outpatient settings and for long-term treatment with minimal risks of major bleeding, which is an important step in improving the quality of life of cancer patients.



Cardiotoxicity and chronic heart failure in the treatment of patients with gastric cancer: pathogenesis, methods of prevention and therapy
Abstract
Chronic heart failure (CHF) is a serious complication of chemotherapy in cancer patients, including patients with gastric cancer (GC). With the increase in overall survival of such patients, the relevance of diagnosis and treatment of concomitant cardiovascular complications increases, which has led to the formation of a new discipline – cardiooncology. This survey research analyzes the mechanisms of pathogenesis, modern approaches to the prevention and treatment of CHF in the context of cardiotoxicity caused by chemotherapy for GC. An important role in the management of cardiac complications is played by timely diagnostics and a risk-adapted approach to the appointment of cardioprotectors, taking into account both standard risk factors for heart disease and the side effects of antitumor drugs. Therapeutic approaches to the treatment of type I and type II cardiotoxicity may differ; in the latter case, sometimes it is enough to discontinue the chemotherapeutic drug to restore cardiac function. Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers are usually considered as first-line drugs and/or in combination with β-blockers. In general, therapy for CHF in patients with gastric cancer should comply with the general principles of international clinical guidelines for cardiology and cardiooncology and be carried out in close cooperation between an oncologist and a cardiologist.



New trends in kidney tumor diagnostics (literature review)
Abstract
Renal cell carcinoma (RCC) is one of the most common oncourological diseases and ranks 10th among malignant neoplasms in the world and 3rd among malignant neoplasms of the genitourinary system (EAU Guidelines, 2017). According to B.P. Matveev (2011), over the past decades, there has been a tendency to increase RCC by 2–4% per year in all population groups. This is attributable to both a true increase in a number of oncourological patients and the improvement of modern diagnostic capabilities. However, despite a significant number of patients with early identified tumor process, the mortality rate from the disease remains high. The only effective method of treating RCC is surgery, which involves nephrectomy or resection of the kidney with the tumor, but in 68.1% of patients with localized and locally advanced forms of the disease, according to B.P. Matveev (2011), tumor process progresses after radical treatment at various times. High incidence rate, large number of relapses, variability of the course of the tumor process after surgery and the lack of a single prognostic system with high accuracy determine the relevance of the problem and indicate the need to create a prognostic panel of factors that can accurately predict the course of the disease after surgery for RCC. The objective of the review is to determine the diagnostic value of CT angiography and CT perfusion in optimizing surgical treatment tactics and assessing the functional capacity of the renal parenchyma in RCC. The search results in the PubMed, Medline, Web of Science scientific databases for the queries «renal parenchyma cancer», «diagnosis of kidney tumors» were analyzed. The review provides detailed consideration and illustration of prognostic factors for the course of the disease in locally advanced renal cancer and the diagnostic value of CT angiography and CT perfusion in determining tumor invasion of intrarenal vessels.
Conclusion. Despite the long history of studying renal parenchymal cancer, there are still no reliable data on the diagnosis of kidney tumors and various prognostic factors for the course of RCC, therefore, the article analyzes and collects the results of recent studies.



Clinical experience
Algorithm for diagnostics and systemic therapy of metastatic hormone-sensitive HER2-negative breast cancer
Abstract
Modern methods of systemic therapy of metastatic breast cancer (mBC) include the use of various combinations of chemotherapy, hormonal therapy, targeted and immunotherapy. The development and introduction of new therapeutic agents continue to change the standards of treatment and open new horizons for an individualized approach to therapy. This article considers the features of diagnostics, available treatment options for hormone-sensitive HER2-negative mBC and promising new treatment methods.



Possibility of de-escalation of adjuvant chemotherapy in patients with colorectal cancer taking into account the ctDNA determination
Abstract
Background. The role of adjuvant chemotherapy in patients with stage IIA colorectal cancer (CRC) remains questionable, since this treatment strategy does not lead to an increase in overall survival. However, if at least one unfavorable prognosis factor is present, postoperative chemotherapy is still recommended. Currently, the global oncology community recognizes that this approach is not reliable and has a low level of evidence. Thus, the search for new predictive factors that can become a reliable tool when deciding whether to prescribe or refuse adjuvant chemotherapy continues. Determination of circulating tumor DNA (ctDNA) is one of the most promising areas. The article presents current literature data on the possibility and feasibility of determining ctDNA in patients with stage IIA colorectal cancer, which will allow optimizing postoperative treatment tactics.
Conclusion. Today, the ctDNA determination has become an important prognostic marker, which in the future can influence the management strategy of cancer patients both in the direction of escalation and de-escalation of treatment, protect some patients from overtreatment and, conversely, accurately select patients for more intensive treatment options.



Nasopharyngeal cancer. ESMO 2024 news
Abstract
Nasopharyngeal cancer (NPC) belongs to the group of orphan malignant neoplasms. This nosology is characterized by a modest arsenal of treatment options for both localized and widespread forms. The above facts explain the extremely unsatisfactory results of treatment of patients with nasopharyngeal carcinoma. Major recent international conferences have not presented breakthrough studies in this area beyond the Chinese protocols using chemo-immunotherapy for recurrent/metastatic forms of the disease. The exception was the latest congress of the European Society of Medical Oncology (ESMO), which was held from September 13 to 17 in Barcelona, Spain. In this review article, we discuss the most significant studies on the treatment of patients with nasopharyngeal carcinoma that were reported at ESMO 2024 and may change the routine practice of an oncologist in the near future.



Original articles
Efficacy of ramucirumab in the second-line treatment of patients with disseminated gastric cancer in routine clinical practice in Russia (RAMSELGA observational study)
Abstract
Background. Currently, ramucirumab, an inhibitor of type 2 vascular endothelial growth factor receptors, in combination with paclitaxel is the most effective second-line treatment regimen for disseminated gastric cancer (DGC). The experience of successful use of ramucirumab in real clinical practice in various countries of the world is widely presented in the literature.
Objective. Evaluation of the effectiveness of ramucirumab as monotherapy or in combination with chemotherapy as a second-line treatment for patients with DGC in routine clinical practice in Russia.
Methods. The analysis included data from 163 patients with GC from 11 oncology institutions in Russia who received ramucirumab as part of the second-line treatment: 17 patients were prescribed ramucirumab as a monotherapy, 104 – in combination with paclitaxel, 42 – in combination with irinotecan-based regimens. The treatment efficacy was assessed.
Results. The efficacy of ramucirumab as a monotherapy was: disease stabilization – 47.1%, median progression-free survival (mPFS) – 2.2 months, median overall survival (mOS) – 5.6 months. When treating with ramucirumab in combination with paclitaxel, the objective response rate (ORR) was 24.0% (3,8% complete response), disease control – 76.9%. The median PFS and OS were 6.1 and 10.6 months, respectively. As a result of treatment with ramucirumab in combination with irinotecan-based regimens, the ORR was 26.2% (4.8% complete response), disease control was 88.1%. The median PFS and OS were 7.5 and 13.3 months, respectively.
Conclusion. According to the obtained results, ramucirumab in combination with paclitaxel or the FOLFIRI regimen is an effective option for second-line therapy in DGC. The results of using ramucirumab alone or in combinations in real clinical practice in Russia are not inferior to and even numerically surpass the data from international studies and are comparable with the practical experience of other countries.



Results of therapy of acute lymphoblastic leukemia in children depending on the mutational status of the ABCB1 gene
Abstract
Background. Despite significant evidence of clinical efficacy of modern protocols for the treatment of acute lymphoblastic leukemia (ALL) in children, methotrexate (MTX) in high doses (HD-MTX>1000 mg/m2) is still one of the main components of therapy; significant interindividual variability of disease outcomes have been noted, which determines the possible role of pharmacogenetics (PG) in the identification of polymorphisms in candidate genes.
Objective. To evaluate the efficacy of MTX therapy for pediatric ALL by identifying possible associations of ABCB1 (ATP-binding cassette subfamily B member 1) gene polymorphisms with treatment outcomes.
Methods. A prospective analysis of a database of pediatric patients with ALL in an observational (cohort) single-center study. The study included 124 children diagnosed with ALL who received therapy according to ALL BFM 2002/2009 protocols using HD-MTX. Real-time PCR (polymerase chain reaction) method was used to study ABCB1 gene polymorphisms. The study material was peripheral blood. The material was sampled once regardless of the duration of MTX therapy. SNPs (single nucleotide polymorphisms) selection criteria: minor allele frequency >5%, genes that corresponded to Hardy–Weinberg equilibrium (HWE, Hardy–Weinberg equilibrium) and finally the level of evidence of previously published studies. SPSS Statistics 26.0 (USA). program was used for statistical processing of the results. Survival analysis was performed by the Kaplan-Meier method. In all statistical analysis procedures, the critical level of significance was taken as p<0.05.
Results. Significant associations of increased risk of delayed-onset events were found in carriers of the GG allele of the ABCB1 gene rs2032582 (OR=2.5, 95% CI 1.12–5.5; p=0.023) and the TT polymorphism of the ABCB1 gene rs4148738 (OR=2.4, 95% СI 1.07–5.3; p=0.031). Event-free and relapse-free survival rates were significantly higher in the TT, TC carrier group than in the group of carriers of the CC «wild type» allele of the ABCB1 C3435T rs1045642 gene (p=0.018 and p=0.026 respectively). All three types of estimated survival (EFS, RFS, OS) were higher in the group of patients receiving MTX at a dose of more than 1000 mg/m2 (p<0.001, p<0.001, p=0.047 respectively).
Conclusion. The need for innovative approaches, including the determination of polymorphisms of genes providing transport and metabolism of cytostatics, to further increase patient survival while reducing adverse effects of antitumor treatment is undoubted.



Analysis of pharmacotherapy in patients with HR+HER2- metastatic breast cancer with PIK3CA mutations in real clinical practice
Abstract
Background. The most common type of breast cancer (BC) is hormone receptor-positive HER2-negative (HR+ HER2-) tumors, approximately 40% of which have mutations in the PIK3CA oncogene encoding the catalytic subunit of the PI3K protein. The most effective pharmacotherapy for such neoplasms is the use of a combination of PI3Kα-specific inhibitors alpelisib and fulvestrant. However, in real clinical practice, the use of this combination did not become available immediately.
Objective. Retrospective analysis of the efficacy of various drug therapy options in the study cohort of patients in real clinical practice.
Methods. The study included 34 patients with HR+/HER2- metastatic breast cancer with PIK3CA mutation, who received treatment at the Primorsky Regional Oncology Dispensary.
Results. The median EFS in the group receiving CDk4/6 inhibitors was 27.00 months (95% CI: 18.00–78.00), and in the group not receiving CDk4/6 inhibitors it was 8.00 months (95% CI: 3.00–39.00), P=0.020. The median EFS in the alpelisib group was 65.00 months (95% CI: 19.00–78.00), the median EFS in the other therapy group (not receiving alpelisib) was 9.00 months (95% CI: 7.00–27.00). The differences in EFS were statistically significant (P=0.025).
Conclusion. Effective pharmacotherapy options for the study group of patients include the use of both CDk4/6 inhibitors and the PIK3 inhibitor alpelisib in combination with fulvestrant. Despite a number of limitations, the RWD study demonstrated improved survival outcomes for patients who were prescribed any CDk4/6 inhibitor and alpelisib.



Potentials for endoscopic and magnetic resonance diagnostic methods in assessing the radicality of chemoradiotherapy in patients with rectal cancer
Abstract
Background. One of the treatment options for patients with a histologically verified diagnosis of rectal cancer (RC) after chemoradiotherapy (CRT) at the first stage with a complete clinical response is an organ-preserving method consisting in follow-up. Given the possible risks of choosing this observation method, including continued tumor growth, high accuracy in assessing the response to CRT is required. The response of the rectum to CRT is assessed based on the results of a set of physical and instrumental diagnostic methods, including digital rectal examination, rectoscopy, and magnetic resonance imaging (MRI).
Objective. Comparison of the accuracy of the endoscopic examination method, supplemented by mandatory biopsy material collection, and MRI in assessing the complete clinical response after CRT.
Methods. In the period from 2017 to 2023, 117 patients with verified cancer of the middle and lower ampullar parts of the rectum were examined and treated at the N.N. Trapeznikov Research Institute of Cancer Research, N.N. Blokhin National Medical Research Center of Oncology. All patients underwent neoadjuvant CRT at the first stage of complex therapy.
Results. The effectiveness of the therapy was assessed based on the results of a clinical examination, including MRI and colonoscopy with biopsy. The reference standard for assessing the accuracy of the examination results was the conclusion of a histological examination based on the material taken during colonoscopy from the site of a previously localized tumor.
Conclusion. Clinical assessment of the performed CRT using a combination of MRI and endoscopy (+ biopsy) is the most accurate and effective strategy for identifying patients with a residual tumor or patients with a likelihood of continued growth, especially in some cases where it is possible to delay surgical treatment and maintain the patient’s functional status. The addition of MRI (including DWI) to an endoscopic examination improves diagnostic indicators and their combination can be recommended as a diagnostic algorithm after CRT.



Markers of kidney damage in children with acute leukemia after completion of polychemotherapy
Abstract
Background. Long-term consequences of polychemotherapy (PCT) for acute lymphoblastic leukemia (ALL), adversely affecting the kidneys, require study in pediatric practice.
Objective. Evaluation of the markers of kidney damage in children with acute lymphoblastic leukemia after completion of polychemotherapy.
Methods. A cross-sectional study of kidney damage markers in the serum (creatinine and cystatin C) and urine (neutrophil gelatinase-associated lipocalin (NGAL), β2-microglobulin, kidney injury molecule-1 (KIM-1), and interleukin 18 (IL-18)) was conducted in 38 children aged 3–18 years with ALL in the period from 2 weeks to 6.5 years after the end of chemotherapy. The control group included 50 children of the corresponding age and sex, II health group. The data are presented as median and interquartiles (Me [25; 75]), comparison of groups – according to the Mann-Whitney criterion.
Results. A higher serum cystatin C level was found in children with ALL, regardless of the renal filtration function in all studied periods after the end of chemotherapy (p < 0.001). In the first two years after the end of chemotherapy, children with ALL had an increased urine KIM-1 level compared to the control group (p =0.009). In children with ALL after chemotherapy, who have a decrease in eGFR <90 ml/min/1.73 m2 based on the CKiD U25 formula for serum cystatin C using an age-dependent coefficient, an increased urine KIM-1 level (p=0.005) and its normalized value – urine KIM-1/ creatinine ratio (p=0.016) were observed.
Conclusion. An increase in the serum cystatin C levels for 6.5 years after chemotherapy and urine KIM-1 levels in the first two years after the end of therapy may indicate persistent changes in the glomeruli and tubules of the kidneys and serve as predictors of the development of CKD in children.



Алгоритмы
Algorithm for diagnosis and treatment of small-cell lung cancer (SCLC)



Clinical case
The potential of SPECT/CT examination in detecting benign bone changes using clinical cases as an example
Abstract
Bone scintigraphy is a highly sensitive but low-specific diagnostic method. It is noted that single-photon emission computed tomography combined with computed tomography (SPECT/CT) has greater sensitivity and accuracy compared to planar scintigraphy. The article presents differential diagnostics of focal bone changes detected by planar bone scintigraphy using clinical cases, carried out using the hybrid diagnostic method SPECT/CT, due to which benign changes in the skeletal system were detected. Thus, SPECT/CT examination allows to detect not only foci of malignant neoplasms, but also changes of benign nature, which is especially important in differential diagnostics of malignant and benign neoplasms.



A rare clinical case: treatment of a mediastinal tumor without organospecificity
Abstract
The incidence of malignant neoplasms is steadily increasing every year. In addition to common localizations, oncologists encounter non-standard tumors that require a personalized approach to treatment depending on the clinical situation. In recent decades, there has been significant progress in the creation of pharmacological drugs that are successfully used in the treatment of cancer, which selectively affect various targets in tumor cells. The article presents a clinical case of diagnosis and treatment of an anterior mediastinal tumor without organospecificity. An effective option for drug therapy aimed at targets found in tumor cells is described. The presented example demonstrates an individualized approach to the choice of treatment for a cancer patient and the effectiveness of its use.



Case report: long-term response to osimertinib in metastatic non-small cell lung cancer with a rare mutation in EGFR gene exon 20
Abstract
Mutations in the epidermal growth factor receptor (EGFR) gene are present in more than 15–20% of patients with non-small cell lung cancer (NSCLC). These are mostly classical activating mutations – deletions in exon 19 and L858R point mutations in exon 21. Both mutations are sensitive to EGFR tyrosine kinase inhibitors (TKIs), which have become the accepted standard of first-line treatment for advanced EGFR-mutated NSCLC. However, 10 to 20% of EGFR-positive NSCLC cases have less common mutations, including exon 20 mutations, for which the response to EGFR TKI therapy can vary significantly depending on the type of mutation, and the choice of optimal therapy remains a challenge. Here, we present a description of a clinical case of successful and durable response to first-generation (within a year) and then third-generation (more than 7 years) TKI therapy in metastatic NSCLC with a rare EGFR exon 20 mutation. Treatment is still ongoing.



Cardiotoxicity of doxorubicin in a child with acute leukemia
Abstract
The introduction of innovative drug therapy regimens for blood cancers in children has increased life expectancy and event-free survival. An integral component of most modern antitumor therapy regimens used in pediatric oncology are anthracycline antibiotics, the effectiveness of which has been clinically proven. The use of drugs in this group is associated with the development of side effects, such as cardiotoxicity. Clinical manifestations of cardiotoxicity manifest as impaired myocardial contractile function and cardiomyopathy with congestive heart failure, arrhythmias and can lead to a reduction in life expectancy. The article presents a clinical case of cardiotoxicity of an anthracycline drug with the development of dilated cardiomyopathy and heart failure in a patient with acute lymphoblastic leukemia. Timely detection of clinical signs of cardiotoxicity and the use of cardioprotective therapy improved the prognosis of the disease and the patient’s quality of life.



Chemotherapy in patients with advanced gastrointestinal tumors and end-stage chronic kidney disease. Brief literature review and clinical case reports
Abstract
Background. Patients with chronic kidney disease (CKD) on hemodialysis (HD) often face difficulties in the use of chemotherapy (CT), since most antitumor drugs have nephrotoxicity, which can worsen the condition of the kidneys. At the same time, there are no clear recommendations for the management of patients in this category. The article presents current information on the management of patients receiving CT against the background of HD, assesses the possibility of CT in patients with gastrointestinal tract (GIT) tumors against the background of the end-stage CKD receiving HD, and gives recommendations for individual treatment adjustment using the example of two clinical cases of patients with end-stage CKD receiving HD and CT.
Results. Both patients showed positive dynamics: the first patient had a partial tumor response to treatment, the second patient had stabilization of the process. However, the treatment was accompanied by various manifestations of toxicity, including stomatitis, asthenia and diarrhea, which required further dose adjustment. An important role was played by the pharmacokinetics of antitumor drugs, which was taken into account when prescribing CT in the conditions of program HD.
Discussion. CT in patients with CKD on HD can be successful if the pharmacokinetics of the drugs, regular monitoring and dose adjustment are taken into account. Platinum derivatives and 5-fluorouracil, used in the treatment of gastrointestinal tumors, require special attention in conditions of renal failure. Nevertheless, dose adjustment and HD before and after drug administration provide achieving therapeutic efficacy while minimizing side effects.
Conclusion. The end-stage CKD and the need for program HD are not an absolute contraindication to CT in patients with gastrointestinal tumors. An individual approach to each patient, dose adjustment and careful monitoring of the patient’s condition provide achieving positive results in antitumor treatment.


