Breast cancer staging in a single session: Whole-body PET/CT mammography

被引:102
作者
Heusner, Till A. [1 ]
Kuemmel, Sherko [2 ]
Umutlu, Late [1 ]
Koeninger, Angela [2 ]
Freudenberg, Lutz S. [3 ]
Hauth, Elke A. M. [1 ]
Kimmig, Klaus R. [2 ]
Forsting, Michael [1 ]
Bockisch, Andreas [3 ]
Antoch, Gerald [1 ]
机构
[1] Univ Duisburg Essen, Dept Diagnost & Intervent Radiol & Neuroradiol, Univ Hosp Essen, Essen, Germany
[2] Univ Duisburg Essen, Dept Gynecol & Obstet, Univ Hosp Essen, Essen, Germany
[3] Univ Duisburg Essen, Dept Nucl Med, Univ Hosp Essen, Essen, Germany
关键词
breast cancer; oncology; PET/CT; whole-body imaging; mammography;
D O I
10.2967/jnumed.108.052050
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 [临床医学]; 100207 [影像医学与核医学]; 1009 [特种医学];
摘要
Our objective was to compare the diagnostic accuracy of an all-in-one protocol of whole-body F-18-FDG PET/CT and integrated F-18-FDG PET/CT mammography with the diagnostic accuracy of a multimodality algorithm for initial breast cancer staging. Methods: Forty women (mean age, 58.3 y; range, 30.8-78.4 y; SD, 12 y) with suspected breast cancer were included. For the primary tumor, we compared F-18-FDG PET/CT mammography versus MRI mammography; for axillary lymph node status, F-18-FDG PET/CT versus clinical investigation and ultrasound; and for distant metastases, F-18-FDG PET/CT versus a multimodality staging algorithm. Histopathology and clinical follow-up served as the standard of reference. The Fisher exact test evaluated the significance of differences (P < 0.05). Alterations in patient management caused by F-18-FDG PET/CT were documented. Results: No significant differences were found in the detection rate of breast cancer lesions (F-18-FDG PET/CT, 95%; MRI, 100%; P = 1). F-18-FDG PET/CT correctly classified lesion focality significantly more often than did MRI (F-18-FDG PET/CT, 79%; MRI, 73%; P < 0.001). MRI correctly defined the T stage significantly more often than did F-18-FDG PET/CT (MRI, 77%; F-18-FDG PET/CT, 54%; P = 0.001). F-18-FDG PET/CT detected axillary lymph node metastases in 80% of cases; clinical investigation/ultrasound, in 70%. This difference was not statistically significant (P = 0.067). Distant metastases were detected with F-18-FDG PET/CT in 100% of cases, and the multimodality algorithm identified distant metastases in 70%. This difference was not statistically significant (P = 1). Three patients had extraaxillary lymph node metastases that were detected only by PET/CT (cervical, retroperitoneal, mediastinal/internal mammary group). F-18-FDG PET/CT changed patient management in 12.5% of cases. Conclusion: Our data suggest that a whole-body F-18-FDG PET/CT mammography protocol may be used for staging breast cancer in a single session. This initial assessment of the F-18-FDG PET/CT protocol indicates similar accuracy to MRI for the detection of breast cancer lesions. Although MRI seems to be more accurate when assessing the T stage of the tumor, F-18-FDG PET/CT seems able to more accurately define lesion focality. Although F-18-FDG PET/CT mammography was able to detect axillary lymph node metastases with a high sensitivity, this method cannot soon be ex-pected to replace the combination of clinical examination, ultrasound, and sentinel lymph node biopsy for axillary assessment.
引用
收藏
页码:1215 / 1222
页数:8
相关论文
共 38 条
[1]
Agnese Doreen M, 2005, Surg Technol Int, V14, P51
[2]
[Anonymous], INT J RAD ONCOL BIOL
[3]
Dual-modality PET/CT scanning with negative oral contrast agent to avoid artifacts: Introduction and evaluation [J].
Antoch, G ;
Kuehl, H ;
Kanja, J ;
Lauenstein, TC ;
Schneemann, H ;
Hauth, E ;
Jentzen, W ;
Beyer, T ;
Goehde, SC ;
Debatin, JF .
RADIOLOGY, 2004, 230 (03) :879-885
[4]
Whole-body dual-modality PET/CT and whole-body MRI for tumor staging in oncology [J].
Antoch, G ;
Vogt, FM ;
Freudenberg, LS ;
Nazaradeh, F ;
Goehde, SC ;
Barkhausen, J ;
Dahmen, G ;
Bockisch, A ;
Debatin, JF ;
Ruehm, SG .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (24) :3199-3206
[5]
Breast imaging with positron emission tomography and fluorine-18 fluorodeoxyglucose:: Use and limitations [J].
Avril, N ;
Rosé, CA ;
Schelling, M ;
Dose, J ;
Kuhn, W ;
Bense, S ;
Weber, W ;
Ziegler, S ;
Graeff, H ;
Schwaiger, M .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (20) :3495-3502
[6]
Avril Norbert, 1999, Clin Positron Imaging, V2, P261, DOI 10.1016/S1095-0397(99)00032-1
[7]
FDG-PET as a "metabolic biopsy" tool in non-lung lesions with indeterminate biopsy [J].
Beggs, AD ;
Hain, SF ;
Curran, KM ;
O'Doherty, MJ .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2002, 29 (04) :542-546
[8]
Serial integrated 18F-fluorodeoxythymidine PET/CT monitoring neoadjuvant chemotherapeutic response in invasive ductal carcinoma [J].
Beresford, Mark ;
Lyburn, Iain ;
Sanghera, Bal ;
Makris, Andreas ;
Wong, Wai-Lup .
BREAST JOURNAL, 2007, 13 (04) :424-425
[9]
Diagnostic accuracy of mammography, clinical examination, US, and MR imaging in preoperative assessment of breast cancer [J].
Berg, WA ;
Gutierrez, L ;
NessAiver, MS ;
Carter, WB ;
Bhargavan, M ;
Lewis, RS ;
Ioffe, OB .
RADIOLOGY, 2004, 233 (03) :830-849
[10]
Dual-modality PET/CT imaging: the effect of respiratory motion on combined image quality in clinical oncology [J].
Beyer, T ;
Antoch, G ;
Blodgett, T ;
Freudenberg, LF ;
Akhurst, T ;
Mueller, S .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2003, 30 (04) :588-596