Department of Radiology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa 236-0004, Japan.
Radiology. 2012 Apr;263(1):53-63. doi: 10.1148/radiol.12111177.
To clarify whether fluorine 18 ((18)F) fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) and dynamic contrast-enhanced (DCE) magnetic resonance (MR) imaging performed after two cycles of neoadjuvant chemotherapy (NAC) can be used to predict pathologic response in breast cancer.
Institutional human research committee approval and written informed consent were obtained. Accuracy after two cycles of NAC for predicting pathologic complete response (pCR) was examined in 142 women (mean age, 57 years: range, 43-72 years) with histologically proved breast cancer between December 2005 and February 2009. Quantitative PET/CT and DCE MR imaging were performed at baseline and after two cycles of NAC. Parameters of PET/CT and of blood flow and microvascular permeability at DCE MR were compared with pathologic response. Patients were also evaluated after NAC by using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 based on DCE MR measurements and European Organization for Research and Treatment of Cancer (EORTC) criteria and PET Response Criteria in Solid Tumors (PERCIST) 1.0 based on PET/CT measurements. Multiple logistic regression analyses were performed to examine continuous variables at PET/CT and DCE MR to predict pCR, and diagnostic accuracies were compared with the McNemar test.
Significant decrease from baseline of all parameters at PET/CT and DCE MR was observed after NAC. Therapeutic response was obtained in 24 patients (17%) with pCR and 118 (83%) without pCR. Sensitivity, specificity, and accuracy to predict pCR were 45.5%, 85.5%, and 82.4%, respectively, with RECIST and 70.4%, 95.7%, and 90.8%, respectively, with EORTC and PERCIST. Multiple logistic regression revealed three significant independent predictors of pCR: percentage maximum standardized uptake value (%SUV(max)) (odds ratio [OR], 1.22; 95% confidence interval [CI]: 1.11, 1.34; P < .0001), percentage rate constant (%k(ep)) (OR, 1.07; CI: 1.03, 1.12; P = .002), and percentage area under the time-intensity curve over 90 seconds (%AUC(90)) (OR, 1.04; CI: 1.01, 1.07; P = .048). When diagnostic accuracies are compared, PET/CT is superior to DCE MR for the prediction of pCR (%SUV(max) [90.1%] vs %κ(ep) [83.8%] or %AUC(90) [76.8%]; P < .05).
The sensitivities of %SUV(max) (66.7%), %k(ep) (51.7%), and %AUC(90) (50.0%) at (18)F-FDG PET/CT and DCE MR after two cycles of NAC are not acceptable, but the specificities (96.4%, 92.0%, and 95.2%, respectively) are high for stratification of pCR cases in breast cancer.
阐明氟 18(18F)氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)/计算机断层扫描(CT)和动态对比增强(DCE)磁共振(MR)成像在两个周期新辅助化疗(NAC)后是否可用于预测乳腺癌的病理反应。
本研究获得了机构人类研究委员会的批准和书面知情同意。2005 年 12 月至 2009 年 2 月期间,对 142 名经组织学证实患有乳腺癌的女性(平均年龄 57 岁:范围 43-72 岁)进行了两个周期 NAC 后预测病理完全缓解(pCR)的准确性检查。基线和两个周期 NAC 后进行定量 PET/CT 和 DCE MR 成像。比较 PET/CT 和 DCE MR 的血流和微血管通透性参数与病理反应。根据 DCE MR 测量的实体肿瘤反应评估标准(RECIST)1.1 和欧洲癌症研究与治疗组织(EORTC)标准以及基于 PET/CT 测量的实体肿瘤 PET 反应标准(PERCIST)1.0,在 NAC 后对患者进行评估。采用多变量逻辑回归分析评估 PET/CT 和 DCE MR 上的连续变量,以预测 pCR,并通过 McNemar 检验比较诊断准确性。
NAC 后,所有 PET/CT 和 DCE MR 上的参数均从基线显著下降。24 名患者(17%)获得 pCR,118 名患者(83%)未获得 pCR。RECIST 和 EORTC 及 PERCIST 的灵敏度、特异性和准确性分别为 45.5%、85.5%和 82.4%,70.4%、95.7%和 90.8%。多变量逻辑回归显示 pCR 的三个独立预测因子:最大标准化摄取量百分比(%SUV(max))(比值比[OR],1.22;95%置信区间[CI]:1.11,1.34;P<0.0001)、速率常数百分比(%k(ep))(OR,1.07;CI:1.03,1.12;P=0.002)和 90 秒时时间-强度曲线下面积百分比(%AUC(90))(OR,1.04;CI:1.01,1.07;P=0.048)。当比较诊断准确性时,PET/CT 优于 DCE MR 预测 pCR(%SUV(max)[90.1%]与 %k(ep)[83.8%]或 %AUC(90)[76.8%];P<0.05)。
氟 18 FDG PET/CT 和 DCE MR 在两个周期 NAC 后测量的%SUV(max)(66.7%)、%k(ep)(51.7%)和 %AUC(90)(50.0%)的灵敏度不可接受,但特异性(96.4%、92.0%和 95.2%)很高,可用于分层乳腺癌的 pCR 病例。