허승재 교수
Seung Jae Heo
성균관대학교 의학과 · 의학
연구실 소개
허승재 교수의 연구실은 난소암, 자궁경부암 등 소견암의 정밀 방사선 치료 기법 개발에 초점을 맞추고 있으며, 특히 FDG-PET/CT 기반 3차원 보조치료 계획 및 인체 내 장기의 변형 영향을 분석하는 고도화된 방사선 치료 기술을 연구하고 있습니다. 뿌리 깊은 암 생물학적 기전 탐색과 함께, 방사선 감수성 향상제 및 고용량 방사선 치료 전략의 임상적 유효성도 함께 탐구하고 있습니다. 특히, 방사선 치료의 정밀도와 안전성을 높이기 위한 영상 유도 치료 기법과 조직 반응 분석이 핵심 연구 주제입니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Lymph node metastasis was a poor prognostic factor and adjuvant RT may be useful in patients with microscopic residual tumor. However, because there were high loco-regional recurrences, additional study is needed to determine more effective RT such as increased RT dose or use of radiosensitizers.
The use of IMRT is steadily increasing to treat cancer and is concentrated in metropolitan areas.
Patterns of cancer incidence, use of radiotherapy and infrastructure, and national HIS are very similar between Korea and Japan. However, there are some differences in health insurance management systems for advanced radiation technologies.
This study sought to evaluate the differential effects of bladder distention on point A-based (AICBT) and three-dimensional conformal intracavitary brachytherapy (3D-ICBT) planning for cervical cancer. Two sets of CT scans were obtained for ten patients to evaluate the effect of bladder distention. After the first CT scan, with an empty bladder, a second set of CT scans was obtained with the bladder filled. The clinical target volume (CTV), bladder, rectum, and small bowel were delineated on eac
The aim of the study was to evaluate the treatment outcomes in cervical cancer patients treated with 18F-fluorodeoxyglucose (FDG)-positron emission tomography (PET)/computed tomography (CT)-guided 3-dimensional brachytherapy (3D-BT) planning for the first brachytherapy session.We retrospectively analyzed 87 patients with cervical cancer who received definitive radiotherapy (RT). Primary tumor size was ≤4 cm in 22 patients (25.3%), >4 cm and ≤6 cm in 45 patients (51.7%), and >6 cm in 20 patients
BACKGROUND: A putative tumor suppressor gene at chromosome 10p15, which contains KLF6 and other genes, is predicted to be lost during melanoma development, and its identity is unknown. In this study, we investigated the biological roles and identity of this tumor suppressor gene. METHODS: The human UACC 903 melanoma cell line containing introduced DNA fragments from the 10p15 region with (10E6/3, 10E6/11, and 10E6/18) and without (10ER4S.2/1) the tumor suppressor gene was used. Xenograft tumors
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