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BIOMARKER:

RET fusion

i
Other names: RET, Ret Proto-Oncogene, Proto-Oncogene Tyrosine-Protein Kinase Receptor Ret, Cadherin-Related Family Member 16, Rearranged During Transfection, RET Receptor Tyrosine Kinase, Cadherin Family Member 12, Proto-Oncogene C-Ret, CDHF12, CDHR16, PTC, Ret Proto-Oncogene (Multiple Endocrine Neoplasia And Medullary Thyroid Carcinoma 1, Hirschsprung Disease), Multiple Endocrine Neoplasia And Medullary Thyroid Carcinoma 1, Hirschsprung Disease 1, RET-ELE1, HSCR1, MEN2A, MEN2B, RET51, MTC1
Entrez ID:
Related tests:
1d
The correlation between fine needle aspiration diagnosis and postoperative histopathological results of pediatric thyroid nodules based on the Bethesda system. (PubMed, Front Endocrinol (Lausanne))
The Bethesda system provides high diagnostic accuracy for definitive cytological categories in pediatric thyroid nodules. Even indeterminate categories carry elevated malignancy risk, supporting careful surgical consideration and the value of BRAF V600E testing for preoperative risk stratification.
Retrospective data • Journal
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BRAF (B-raf proto-oncogene) • RET (Ret Proto-Oncogene) • TERT (Telomerase Reverse Transcriptase) • RAS (Rat Sarcoma Virus)
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BRAF V600E • BRAF V600 • RET fusion • RAS mutation • RET mutation
2d
Phase III Study of SY-5007, a RET Inhibitor, in Patients With Locally Advanced or Metastatic RET Fusion-positive NSCLC (clinicaltrials.gov)
P3, N=120, Active, not recruiting, Shouyao Holdings (Beijing) Co. LTD | Recruiting --> Active, not recruiting
Enrollment closed
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RET (Ret Proto-Oncogene)
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RET fusion • RET positive
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soxataltinib (SY-5007)
2d
Study of SNH-118110 in Advanced Solid Tumors (clinicaltrials.gov)
P1, N=240, Not yet recruiting, ScinnoHub Pharmaceutical Co., Ltd.
New P1 trial
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RET (Ret Proto-Oncogene)
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RET fusion
6d
Observed RET-Positive Findings Across Routine Comprehensive Genomic Profiling Platforms in Japan: A Nationwide Descriptive Benchmark. (PubMed, Cancers (Basel))
This nationwide analysis benchmarks how RET-positive findings are surfaced to clinicians across heterogeneous routine CGP implementations in Japan. The data support platform-aware interpretation of RET results in practice, but should not be construed as biologic prevalence estimates or comparative assay performance.
Journal
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RET (Ret Proto-Oncogene)
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RET fusion • RET positive
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FoundationOne® CDx • FoundationOne® Liquid CDx • OncoGuide™ NCC Oncopanel System
6d
Performance of Seven-Gene Panel Testing for Risk Stratification of Thyroid Nodules with Indeterminate Cytology Results. (PubMed, Int J Mol Sci)
Depending on the Bethesda category, the positive predictive value for malignancy of the seven-gene panel ranged between 18.18% (Bethesda III) and 91.07% (Bethesda V), while the negative predictive value ranged between 93.92% (Bethesda III) and 24.14% (Bethesda V). In conclusion, molecular testing with the seven-gene panel can improve ROM estimation in cytopathologically indeterminate thyroid nodules, but its clinical utility depends on the detected gene alteration.
Journal
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KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • NRAS (Neuroblastoma RAS viral oncogene homolog) • RET (Ret Proto-Oncogene) • HRAS (Harvey rat sarcoma viral oncogene homolog) • RAS (Rat Sarcoma Virus) • NCOA4 (Nuclear Receptor Coactivator 4) • PPARG (Peroxisome Proliferator Activated Receptor Gamma) • PAX8 (Paired box 8)
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BRAF V600E • KRAS mutation • NRAS mutation • BRAF V600 • RET fusion • RAS mutation • RET mutation • HRAS mutation
6d
Association of common genetic alterations with tumor recurrence in papillary thyroid cancer. (PubMed, J Natl Cancer Inst)
RET fusions and genetic alteration combination are independent prognostic markers for tumor recurrence of PTC, integrating tumors' genetic status into the 2025 ATA RSS system improves the accuracy of risk stratification for PTC.
Journal
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BRAF (B-raf proto-oncogene) • RET (Ret Proto-Oncogene) • RAS (Rat Sarcoma Virus) • NTRK (Neurotrophic receptor tyrosine kinase)
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BRAF V600E • BRAF V600 • RET fusion • RAS mutation • NTRK fusion
7d
New P2 trial
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EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • PD-L1 (Programmed death ligand 1) • BRAF (B-raf proto-oncogene) • ALK (Anaplastic lymphoma kinase) • MET (MET proto-oncogene, receptor tyrosine kinase) • RET (Ret Proto-Oncogene) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS) • NTRK (Neurotrophic receptor tyrosine kinase)
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PD-L1 expression • BRAF V600E • BRAF V600 • EGFR L858R • HER-2 mutation • RET fusion • MET exon 14 mutation • ALK fusion • RET mutation • ROS1 fusion • HER-2 exon 20 mutation • NTRK fusion
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Focus V (anlotinib) • Andewei (benmelstobart)
10d
SX-682 and Atezolizumab for the Treatment of Advanced or Metastatic, Recurrent Non-small Cell Lung Cancer (clinicaltrials.gov)
P2, N=32, Not yet recruiting, University of Washington | Initiation date: Jun 2026 --> Sep 2026
Trial initiation date • Checkpoint inhibition
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ALK (Anaplastic lymphoma kinase) • RET (Ret Proto-Oncogene) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS) • CXCL8 (Chemokine (C-X-C motif) ligand 8)
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RET fusion • ALK fusion • ROS1 fusion
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SX-682 • Tecentriq Hybreza (atezolizumab and hyaluronidase-tqjs)
13d
Targeted therapy combined with local consolidative surgery for oligometastatic stage IVA lung adenocarcinoma with CCDC6-RET fusion: a case report. (PubMed, Front Oncol)
This case demonstrates that for selected patients with advanced lung adenocarcinoma harboring a CCDC6-RET fusion and oligometastatic disease, initial systemic therapy with selpercatinib followed by local consolidative surgery is a feasible multimodal strategy. This is not a routine recommendation for stage IV lung cancer but requires individualized decision-making after multidisciplinary discussion in specific oligometastatic cases.
Journal
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RET (Ret Proto-Oncogene) • CCDC6 (Coiled-Coil Domain Containing 6)
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RET fusion • CCDC6-RET fusion
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Retevmo (selpercatinib)
14d
RET Fusion-Positive Solid Tumor (PubMed, Gan To Kagaku Ryoho)
Selpercatinib, a RET inhibitor, is covered by insurance for all solid tumors that are positive for the RET fusion gene...In other solid tumors, positivity is less than 0.5%. However, if positive, treatment is expected to be effective, so it is desirable to actively perform cancer gene panel testing.
Journal
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RET (Ret Proto-Oncogene)
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RET fusion • RET positive
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Retevmo (selpercatinib)
14d
Durable response to selpercatinib in HOOK3-RET fusion positive, α-fetoprotein producing metastatic pancreatic ductal adenocarcinoma with intestinal-type differentiation. (PubMed, Oncol Lett)
The patient did not respond to gemcitabine and cisplatin-based systemic chemotherapy. Selpercatinib, a selective inhibitor of receptor tyrosine kinase RET, blocks RET kinase activity by binding to its adenosine triphosphate-binding site, thus preventing the kinase from phosphorylating substrates and halting oncogenic signaling. The patient was treated with selpercatinib, which produced a durable response lasting over 15 months in this chemotherapy-refractory patient, highlighting the efficacy of selpercatinib in HOOK3-RET fusion-positive pancreatic cancer.
Journal
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RET (Ret Proto-Oncogene) • AFP (Alpha-fetoprotein)
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RET fusion • RET positive
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cisplatin • gemcitabine • Retevmo (selpercatinib)
14d
RET fusion partners dictate oncogenic potential in undifferentiated spindle cell sarcomas. (PubMed, Cancer Biol Ther)
Continuous genomic monitoring is essential for identifying resistance mechanisms and guiding precision therapy. Future studies should explore the impact of different fusion partners on tumor behavior and therapeutic response.
Journal
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RET (Ret Proto-Oncogene) • NTRK1 (Neurotrophic tyrosine kinase, receptor, type 1) • CCDC6 (Coiled-Coil Domain Containing 6) • NTRK (Neurotrophic receptor tyrosine kinase)
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RET fusion • RET rearrangement