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BMC Cancer. 2011;11:452.

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

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제1저자 김범석 · 교신저자 임석아

소속 (1)
  1. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

Abstract

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.

Figures

Figure 1
Figure 1 Schematic flow of the neoadjuvant chemotherapy and response assessed by FDG PET/CT, breast MRI and chest CT. Abbreviations: DD, docetaxel+doxorubicin; FDG PET, fluorine-18 fluorodeoxyglucose positron emission tomography; CT, computed tomography; MRI, magnetic resonance imaging; USG, ultrasonography.
Figure 2
Figure 2 Receiver-operating characteristics (ROC) analysis, determine optimal cut-off values of ΔSUV%; Area under the curve ROC was 0.79 (95% confidence interval 0.64-0.93).
Figure 3
Figure 3 Box flows comparing serial FDG PET/CT results according to molecular phenotypes based on immunohistochemistry. ER negative phenotype showed higher pre-SUV (A) and Δ SUV% (B) than ER positive phenotype. In patients with high Ki-67 expression, a similar phenomenon was observed in that pre-SUV (C) and Δ SUV% (D) was higher than the low Ki-67 expression group. In triple negative breast cancer (TNBC), pre-SUV (E) was higher than non-TNBC; however, Δ SUV% (F) was not different.

그림 출처: PubMed Central 공개 논문 (PMC3224348)

그 밖의 정보
출판 형태
Clinical Trial, Phase II, Journal Article, Research Support, Non-U.S. Gov't
저널
BMC cancer · eISSN 1471-2407
전자 출판
2011-10-20
MeSH
Adult · Aged · Antineoplastic Agents / therapeutic use · Biomarkers, Tumor / metabolism · Breast Neoplasms / diagnostic imaging / drug therapy / metabolism · Female · Fluorodeoxyglucose F18* · Humans · Middle Aged · Multimodal Imaging* · Neoadjuvant Therapy · Neoplasm Staging · Phenotype* · Positron-Emission Tomography* · Tomography, X-Ray Computed*
Substances
Antineoplastic Agents · Biomarkers, Tumor · Fluorodeoxyglucose F18
데이터
ClinicalTrials.gov: NCT01396655
참고문헌
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