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The BRAF p.V600E mutation represents the most specific marker for papillary thyroid carcinoma and is potentially related to aggressive behavior and persistent disease. alterations other than the p.V600E are less common in thyroid carcinoma and represent an alternative mechanism of BRAF activation with unclear clinical significance. The study aims to describe the frequency and clinicopathologic characteristics of non-V600E mutations in a large cohort (1654 samples) of thyroid lesions characterized by next-generation sequencing. mutations have been found in 20.3% (337/1654) of thyroid nodules, including classic (p.V600E) mutation in 19.2% (317/1654) of samples and non-V600E variants in 1.1% of cases (19/1654). BRAF non-V600E alterations include 5 cases harboring p.K601E, 2 harboring p.V600K substitutions, 2 with a p.K601G variant, and 10 cases with other non-V600E alterations. non-V600E mutations have been reported in one case of follicular adenoma, three cases of conventional papillary thyroid carcinoma, eight cases of follicular variant of papillary carcinomas, one case of columnar cell variant papillary thyroid carcinoma, one case of oncocytic follicular carcinoma, and two bone metastasis of follicular thyroid carcinoma. We confirm that non-V600E mutations are uncommon and typically found in indolent follicular-patterned tumors. Indeed, we show that non-V600E mutations can be found in tumors with metastatic potential. However, in both aggressive cases, the mutations were concomitant with other molecular alterations, such as promoter mutation.
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http://dx.doi.org/10.3390/ijms24044057 | DOI Listing |
Clin Lung Cancer
July 2025
Division of Medical Oncology, Koç University School of Medicine, Istanbul, Turkey.
Background: Real-world data on BRAF-mutant non-small cell lung cancer (NSCLC) remain limited, particularly regarding outcomes with dabrafenib plus trametinib (D + T).
Methods: This multicenter retrospective study included 88 patients with advanced BRAF-mutant NSCLC treated across 30 centers. Clinicopathologic characteristics, treatment outcomes, and safety data were collected and analyzed.
ESMO Open
August 2025
DKFZ-Hector Cancer Institute at the University Medical Center Mannheim, Mannheim, Germany; Division of Personalized Medical Oncology (A420), German Cancer Research Center (DKFZ), German Center for Lung Research (DZL), Heidelberg, Germany; Department of Personalized Oncology, University Hospital Mann
Background: Non-small-cell lung cancer patients with BRAF mutations benefit from targeted and (chemo-)immune therapy. However, treatment of BRAF mutations poses substantial challenges due to biological heterogeneity, different clinicogenomic features and limited therapy outcome data.
Materials And Methods: We conducted a retrospective analysis of BRAF mutation patients in the national Network Genomic Medicine Lung Cancer, assessing treatment outcomes upon targeted and (chemo-)immune therapy.
Front Immunol
July 2025
Department of Oncology, 920th Hospital of Joint Logistics Support Force, People's Liberation Army, Kunming, Yunnan, China.
Pulmonary adenosquamous carcinoma (ASC) is a rare and aggressive subtype of non-small cell lung cancer (NSCLC) with poorly defined molecular characteristics and therapeutic strategies. We present a 63-year-old male patient with stage IVa (cT4N3M1b) lung ASC. Next-generation sequencing (NGS) revealed co-occurring mutations in KRAS G12C, BRAF (non-V600E), PIK3CA, and FLT1.
View Article and Find Full Text PDFCancers (Basel)
June 2025
Molecular Pathology Laboratory Pathos, 400394 Cluj-Napoca, Romania.
Comprehensive molecular profiling is essential for precision oncology in non-small cell lung cancer (NSCLC). However, genomic data from Eastern European populations, including Romania, remain limited. We analyzed 398 consecutive NSCLC cases tested at the PATHOS Molecular Pathology Laboratory (Cluj-Napoca, Romania) between April 2024 and February 2025 using the Ion Torrent™ Genexus™ System and the Oncomine™ Dx Target Test, which evaluates SNVs/indels in 46 genes, fusions in 23 genes, and CNVs in 19 genes from FFPE samples.
View Article and Find Full Text PDFThorac Cancer
March 2025
Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Vrafmurine sarcoma viral oncogene homolog B (BRAF) mutations, including both V600E and non-V600E variants, are infrequent in non-small cell lung cancer (NSCLC), representing approximately 2% of lung adenocarcinomas. Activated BRAF mutations are regarded as an underappreciated oncogenic driver in NSCLC, typically occurring in a mutually exclusive manner with epidermal growth factor receptor (EGFR) mutations, as well as ALK and ROS1 rearrangements. In recent years, advancements in multiple-gene panel testing have demonstrated that EGFR mutations and BRAF mutations can coexist.
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