Powerful prognostic stratification by [18F] fluorodeoxyglucose positron emission tomography in patients with metastatic breast cancer treated with high-dose chemotherapy

被引:64
作者
Cachin, Florent
Prince, H. Miles
Hogg, Annette
Ware, Robert E.
Hicks, Rodney J.
机构
[1] Peter MacCallum Canc Inst, Ctr Mol Imaging, Melbourne, Vic 3002, Australia
[2] Peter MacCallum Canc Inst, Div Haematol & Med Oncol, Melbourne, Vic 3002, Australia
[3] Univ Melbourne, Parkville, Vic 3052, Australia
[4] Canc Ctr Jean Perrin, Dept Nucl Med, Clermont Ferrand, France
关键词
D O I
10.1200/JCO.2005.04.6326
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose This study examines the use of [F-18]fluorodeoxyglucose positron emission tomography (FDG-PET) for the evaluation of the therapeutic response for patients treated with high-dose chemotherapy (HDC) with autologous stem cell transplantation for metastatic breast cancer (MBC) focusing on prognostic stratification. Patients and Methods Forty-seven patients with MBC were treated with a maximum of three cycles of HDC. Therapeutic response was assessed with conventional imaging (Clmg; including a computed tomography in all cases and ultrasound, mammography, and bone scanning as clinically indicated) and by FDG-PET study performed after the last cycle of HDC. Parameters analyzed for predicting survival were FDG-PET and Clmg results, pattern of disease, prior treatment, and HDC regimen. Results Complete responses were observed in 16 patients (37%) with Clmg and 34 patients (72%) with FDG-PET. The FDG-PET result was the most powerful and independent predictor of survival; patients with a negative post-treatment FDG-PET had a longer median survival than patients with a positive FDG-PET (24 months v 10 months; P <.001). By multivariate analysis the relative risk (BR) of death was higher in patients with FD6-PET-positive disease (RR, 5.3), prior anthracycline treatment (RR, 3.3), or with visceral metastasis (RR, 2.4). Conclusion A single FDG-PET study performed after completion of HDC for MBC can powerfully stratify for survival. This may have implications for how we should assess outcome after conventional-dose therapy for MBC and warrants additional study.
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页码:3026 / 3031
页数:6
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