Search Results - "IYEVLEVA, Aglaya G"
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High response rates to neoadjuvant platinum-based therapy in ovarian cancer patients carrying germ-line BRCA mutation
Published in Cancer letters (28-12-2015)“…Highlights • Ovarian carcinomas arising in BRCA1/2 germ-line mutation carriers show high sensitivity to platinum-based neoadjuvant therapy. • Chemonaive…”
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Somatic loss of the remaining allele occurs approximately in half of CHEK2-driven breast cancers and is accompanied by a border-line increase of chromosomal instability
Published in Breast cancer research and treatment (01-04-2022)“…Purpose Germline mutations in CHEK2 gene represent the second most frequent cause of hereditary breast cancer (BC) after BRCA1/2 lesions. This study aimed to…”
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Molecular profiles of BRCA1‐associated ovarian cancer treated by platinum‐based therapy: Analysis of primary, residual and relapsed tumors
Published in International journal of cancer (01-04-2020)“…Our study aimed to analyze the evolution of molecular portraits of BRCA1‐driven ovarian cancer (OC) during treatment. BRCA1 loss‐of‐heterozygosity status (LOH)…”
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Cost-Efficient Detection of NTRK1/2/3 Gene Fusions: Single-Center Analysis of 8075 Tumor Samples
Published in International journal of molecular sciences (17-09-2023)“…The majority of NTRK1, NTRK2, and NTRK3 rearrangements result in increased expression of the kinase portion of the involved gene due to its fusion to an…”
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Discrimination between Complete versus Non-Complete Pathologic Response to Neoadjuvant Therapy Using Ultrasensitive Mutation Analysis: A Proof-of-Concept Study in BRCA1 -Driven Breast Cancer Patients
Published in International journal of molecular sciences (18-01-2023)“…Neoadjuvant chemotherapy (NACT) for breast cancer (BC) often results in pathologic complete response (pCR), i.e., the complete elimination of visible cancer…”
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Molecular testing and targeted therapy for non-small cell lung cancer: Current status and perspectives
Published in Critical reviews in oncology/hematology (01-01-2021)“…[Display omitted] •There are approved targeted drugs for NSCLCs carrying EGFR, BRAF and MET mutations.•NSCLC testing guidelines include the analysis of ALK,…”
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BRAF-mutated clear cell sarcoma is sensitive to vemurafenib treatment
Published in Investigational new drugs (01-10-2015)“…Summary We report a patient with a metastatic relapse of clear cell sarcoma, whose tumor harbored BRAF V600E mutation. Standard chemotherapy with doxorubicin…”
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Efficacy of lorlatinib in lung carcinomas carrying distinct ALK translocation variants: The results of a single-center study
Published in Translational oncology (01-08-2021)“…•In patients with ALK-rearranged NSCLC who received lorlatinib within the compassionate use program, the objective tumor response (OR) and disease control (DC)…”
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High level of miR-21, miR-10b, and miR-31 expression in bilateral vs. unilateral breast carcinomas
Published in Breast cancer research and treatment (01-02-2012)“…We analyzed the expression of several microRNAs (miRs) implicated in breast cancer (BC) pathogenesis (miR-21, miR-10b, miR17-5p, mir-31, miR-155, miR-200c,…”
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Detection of EGFR mutations and EML4‐ALK rearrangements in lung adenocarcinomas using archived cytological slides
Published in Cancer cytopathology (01-07-2013)“…BACKGROUND Although the molecular analysis of epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) in archived lung cancer tissues is…”
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Molecular tests for prediction of tumor sensitivity to cytotoxic drugs
Published in Cancer letters (01-02-2022)“…Chemotherapy constitutes the backbone of cancer treatment. Several predictive assays assist personalized administration of cytotoxic drugs and are recommended…”
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Lack of Response to Imatinib in Melanoma Carrying Rare KIT Mutation р.T632I
Published in Case reports in oncology (23-01-2019)“…Approximately 15% of acral and mucous melanomas carry activating mutations in KIT oncogene. There is a diversity of spectrum of KIT mutations, with some of…”
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Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia
Published in Familial cancer (01-01-2007)“…Previous studies indicate that founder mutations may play a noticeable role in breast cancer (BC) predisposition in Russia. Here we performed a systematic…”
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Cytotoxic and targeted therapy for hereditary cancers
Published in Hereditary cancer in clinical practice (23-08-2016)“…There is a number of drugs demonstrating specific activity towards hereditary cancers. For example, tumors in BRCA1/2 mutation carriers usually arise via…”
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Novel ALK fusion partners in lung cancer
Published in Cancer letters (28-06-2015)“…Highlights • Combination of two distinct PCR assays is a highly reliable approach for detection of both known and new ALK translocations. • Two novel ALK…”
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EGFR mutation in kidney carcinoma confers sensitivity to gefitinib treatment: A case report
Published in Urologic oncology (01-09-2009)“…Abstract Mutations of the epidermal growth factor receptor (EGFR) gene are known to be associated with the pronounced tumor response to EGFR tyrosine kinase…”
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KRAS, NRAS, BRAF, HER2 and MSI Status in a Large Consecutive Series of Colorectal Carcinomas
Published in International journal of molecular sciences (02-03-2023)“…This study aimed to analyze clinical and regional factors influencing the distribution of actionable genetic alterations in a large consecutive series of…”
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Gene rearrangements in consecutive series of pediatric inflammatory myofibroblastic tumors
Published in Pediatric blood & cancer (01-05-2020)“…Background Inflammatory myofibroblastic tumors (IMTs) are exceptionally rare neoplasms, which are often driven by rearranged tyrosine kinases. Methods This…”
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Rapid and Cost-Efficient Detection of RET Rearrangements in a Large Consecutive Series of Lung Carcinomas
Published in International journal of molecular sciences (23-06-2023)“…-kinase-activating gene rearrangements occur in approximately 1-2% of non-small-cell lung carcinomas (NSCLCs). Their reliable detection requires…”
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