Jeeyun Lee
Sungkyunkwan University 의과대학 · Medicine
이 교수의 연구실은 위암의 예후 예측 및 개인화된 치료 전략 개발에 초점을 맞추고 있습니다. 특히, 병행 치료(화학요법 및 방사선 치료)의 효과 분석, 유전자 발현 프로파일을 기반으로 한 예후 알고리즘 개발, 그리고 바이오마커 기반 맞춤형 치료(예: AKT, MET, MEK 억제제)의 임상 적용을 연구하고 있습니다. 또한 PD-L1, MSI, EBV 상태와 같은 면역조절 마커를 통해 면역요법의 적응 환자를 선별하는 데에도 기여하고 있습니다.
Figures are computed from collected data and may differ slightly.
Of 458 patients, 228 were randomly assigned to the XP arm and 230 to the XP/XRT/XP arm. Treatment was completed as planned by 75.4% of patients (172 of 228) in the XP arm and 81.7% (188 of 230) in the XP/XRT/XP arm. Overall, the addition of XRT to XP chemotherapy did not significantly prolong disease-free survival (DFS; P = .0862). However, in the subgroup of patients with pathologic lymph node metastasis at the time of surgery (n = 396), patients randomly assigned to the XP/XRT/XP arm experienc
The newly proposed model for extranodal NK/T-cell lymphoma demonstrated a more balanced distribution of patients into four groups with better prognostic discrimination as compared with the IPI.
The VIKTORY (targeted agent eValuation In gastric cancer basket KORea) trial was designed to classify patients with metastatic gastric cancer based on clinical sequencing and focused on eight different biomarker groups (<i>RAS</i> aberration, <i>TP53</i> mutation, <i>PIK3CA</i> mutation/amplification, <i>MET</i> amplification, MET overexpression, all negative, <i>TSC2</i> deficient, or <i>RICTOR</i> amplification) to assign patients to one of the 10 associated clinical trials in second-line (2L)
Despite the benefits from adjuvant chemotherapy or chemoradiotherapy, approximately one-third of stage II gastric cancer (GC) patients developed recurrences. The aim of this study was to develop and validate a prognostic algorithm for gastric cancer (GCPS) that can robustly identify high-risk group for recurrence among stage II patients. A multi-step gene expression profiling study was conducted. First, a microarray gene expression profiling of archived paraffin-embedded tumor blocks was used to
PD-L1 is expressed in 59.3 % of GC patients and is associated with MSI and EBV positivity. These results provide a basis for identifying GC patients who may benefit from anti-PD-1/PD-L1 therapy.
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