International Conference on Oncology and Cancer Research

Theme: Integrative Oncology: Advancing Personalized Care through Innovation, Ethics, and Global Collaboration Dates: 06 February, 2025 (Physical); 07 February, 2025 (Virtual)    Location: Hotel Holiday Inn Singapore Atrium, 317 Outram Road Singapore, 169075    About the Conference: The International Conference on Oncology and Cancer Research 2025 welcomes researchers, clinicians, academicians, industry experts, and advocates from around the globe to discuss and explore advancements in oncology and cancer research. Under the theme

08 February 2025 Singapore / Virtual
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Ying Xu
Featured Speaker

Ying Xu

Keynote Speaker

China

Biography

Doctor of Surgery Postdoctoral Fellow in Oncology Specialty: diagnosis and treatment of breast and thyroid diseases

Abstract Title

Surgeon-In-Charge, Associate Professor Doctor of Surgery Postdoctoral Fellow in Oncology Specialty: diagnosis and treatment of breast and thyroid diseases, surgical treatment of benign and malignant tumors and comprehensive treatment of malignant tumors, especially familiar with immunotherapy and targeted therapy of breast malignant tumors. Reference: The whole-exon Gene Sequence Application in Clinical Rare Cancers In our clinical working, the multiple primary cancer (MPC) in a single patient occurred increasingly. These patients always possessed particular histopathology, physiology, and clinical symptoms, implicating that the normal treatments might not be suitable for them. To explore the tumorigenesis and prognosis of MPC, we utilized the novel whole-exon gene sequence assay to detect potential mutative genes based on paraffine tumor species from two patients: one of them was diagnosed as thyroid collision tumor (TCT), the other was diagnosed as renal cancer, breast cancer and thyroid papillary cancer. The result showed that a total of 76 single nucleotide variants (SNV), 12 insertion and deletion variants (INDEL), and 99 copy number variations (CNV) were identified in TCT, while only PCMTD with the copy number variation (CNV) was associated with the MPC patient. In summary, these clustered special genes in MPC and TCT disease give us new sight to deeply understand the tumorigenesis and prognosis of rare malignant tumours of patients.