Early metabolic response using FDG PET/CT and molecular phenotypes of breast cancer treated with neoadjuvant chemotherapy

被引:58
|
作者
Keam, Bhumsuk [1 ,2 ]
Im, Seock-Ah [1 ,2 ]
Koh, Youngil [1 ]
Han, Sae-Won [1 ,2 ]
Oh, Do-Youn [1 ,2 ]
Cho, Nariya [4 ]
Kim, Jee Hyun [1 ,2 ]
Han, Wonshik [5 ]
Kang, Keon Wook [2 ,3 ]
Moon, Woo Kyung [4 ]
Kim, Tae-You [1 ,2 ]
Park, In Ae [6 ]
Noh, Dong-Young [5 ]
Chung, June-Key [2 ,3 ]
Bang, Yung-Jue [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 151, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Nucl Med, Seoul, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Radiol, Seoul, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Surg, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 151, South Korea
来源
BMC CANCER | 2011年 / 11卷
基金
新加坡国家研究基金会;
关键词
FDG PET; breast cancer; neoadjuvant chemotherapy; molecular phenotype; POSITRON-EMISSION-TOMOGRAPHY; PATHOLOGICAL RESPONSE; F-18; FLUORODEOXYGLUCOSE; PRIMARY TUMOR; BLOOD-FLOW; PHASE-II; STAGE-II; IN-SITU; DOXORUBICIN; GUIDELINES;
D O I
10.1186/1471-2407-11-452
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This study was aimed 1) to investigate the predictive value of FDG PET/CT (fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography) for histopathologic response and 2) to explore the results of FDG PET/CT by molecular phenotypes of breast cancer patients who received neoadjuvant chemotherapy. Methods: Seventy-eight stage II or III breast cancer patients who received neoadjuvant docetaxel/doxorubicin chemotherapy were enrolled in this study. FDG PET/CTs were acquired before chemotherapy and after the first cycle of chemotherapy for evaluating early metabolic response. Results: The mean pre- and post-chemotherapy standard uptake value (SUV) were 7.5 and 3.9, respectively. The early metabolic response provided by FDG PET/CT after one cycle of neoadjuvant chemotherapy was correlated with the histopathologic response after completion of neoadjuvant chemotherapy (P = 0.002). Sensitivity and negative predictive value were 85.7% and 95.1%, respectively. The estrogen receptor negative phenotype had a higher pre-chemotherapy SUV (8.6 vs. 6.4, P = 0.047) and percent change in SUV (48% vs. 30%, P = 0.038). In triple negative breast cancer (TNBC), the pre-chemotherapy SUV was higher than in non-TNBC (9.8 vs. 6.4, P = 0.008). Conclusions: The early metabolic response using FDG PET/CT could have a predictive value for the assessment of histopathologic non-response of stage II/III breast cancer treated with neoadjuvant chemotherapy. Our findings suggest that the initial SUV and the decline in SUV differed based on the molecular phenotype.
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页数:9
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