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$^{18}F$-FDG PET/CT with Contrast Enhancement for Evaluation of Axillary Lymph Node Involvement in T1 Breast Cancer
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  • $^{18}F$-FDG PET/CT with Contrast Enhancement for Evaluation of Axillary Lymph Node Involvement in T1 Breast Cancer
  • $^{18}F$-FDG PET/CT with Contrast Enhancement for Evaluation of Axillary Lymph Node Involvement in T1 Breast Cancer
저자명
Kong. Eun-Jung,Chun. Kyung-Ah,Cho. Ihn-Ho,Lee. Soo-Jung
간행물명
Nuclear medicine and molecular imaging : NMMI
권/호정보
2010년|44권 3호|pp.170-176 (7 pages)
발행정보
대한핵의학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Background $^{18}F$-fluorodeoxyglucose ($^{18}F$-FDG) positron emission tomography ((PET) safely predicts axillary status in patients with breast cancer, but is not sufficiently accurate in early breast cancer patients. This study analyzed the value of $^{18}F$-FDG PET/computed tomography (CT) with contrast enhancement in detecting axillary lymph node involvement in T1 breast cancer patients. Methods Contrast-enhanced $^{18}F$-FDG PET/CT was performed within 20 days of surgery in 143 breast cancer patients with tumors ${leq}$2 cm in size. The patients underwent either axillary lymph node dissection (ALND) or sentinel lymph node biopsy (SLNB), and histopathology reports were used to provide the definitive diagnosis against which the contrast-enhanced $^{18}F$-FDG PET/CT study results were compared. Results The sensitivity, specificity, and negative and positive predictive values of contrast-enhanced $^{18}F$-FDG PET/CT in detecting axillary involvement were 70.0%, 92.2%, 88.8%, and 77.8%, respectively, in the entire series of 143 patients, with eight false-positive and 12 false negative results. The false-negative results were associated with the number of metastatic lymph nodes and the rate of FDG uptake. Conclusion Contrast-enhanced $^{18}F$-FDG PET/CT cannot replace histologic staging using SLNB in patients with breast cancer, but $^{18}F$-FDG PET/CT increases the sensitivity for predicting axillary node metastasis, and allows for a selective approach to either ALND or SLNB, even in patients with T1 breast cancer.