AJR
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Eubank, W. B.
Right arrow Articles by Livingston, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Eubank, W. B.
Right arrow Articles by Livingston, R.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Impact of FDG PET on Defining the Extent of Disease and on the Treatment of Patients with Recurrent or Metastatic Breast Cancer

William B. Eubank1, David Mankoff2, Mallar Bhattacharya3, Julie Gralow4, Hannah Linden4, Georgiana Ellis4, Skyler Lindsley5, Mary Austin-Seymour5 and Robert Livingston4

1 Department of Radiology, Puget Sound Veterans Affairs Health Care System, 1660 S Columbian Way, S-113-RAD, Seattle, WA 98108.
2 Division of Nuclear Medicine, University of Washington School of Medicine, 1959 NE Pacific St., Seattle, WA 98195-7115.
3 Department of Radiology, University of Washington School of Medicine, Seattle, WA 98195-7115.
4 Division of Medical Oncology, University of Washington School of Medicine, Seattle, WA 98195-7115.
5 Department of Radiation Oncology, University of Washington School of Medicine, Seattle, WA 98195-7115.



View larger version (15K):

[in a new window]
 
Fig. 1. —Bar graph illustrates impact of FDG PET on therapeutic plan by category of referral in 125 patients with advanced breast cancer. Black bars represent patients with locoregional disease, dark gray bars represent patients being evaluated for response to therapy, light gray bars represent patients with equivocal findings on conventional imaging, and white bars represent patients with known metastases being evaluated for extent of disease. Above each category, p values from chi-square analysis of impact of FDG PET on alteration of management plan for each referral category are presented.

 


View larger version (75K):

[in a new window]
 
Fig. 2A. —42-year-old woman who developed recurrence in right mastectomy scar 21 months after surgical resection of infiltrating ductal carcinoma. Results of conventional staging studies (chest CT and bone scan) were negative (not shown). Patient was being considered for aggressive local therapy (surgery and radiation). Coronal image from FDG PET shows uptake in right axilla (arrowhead; maximum standard uptake value [SUV], 6.0).

 


View larger version (96K):

[in a new window]
 
Fig. 2B. —42-year-old woman who developed recurrence in right mastectomy scar 21 months after surgical resection of infiltrating ductal carcinoma. Results of conventional staging studies (chest CT and bone scan) were negative (not shown). Patient was being considered for aggressive local therapy (surgery and radiation). Coronal image from FDG PET shows uptake in mediastinum (arrows; maximum SUV, 2.8). Malignant nodal involvement in mediastinum was confirmed by mediastinoscopy. Because FDG PET indicated more widespread disease than conventional staging examinations, therapeutic plan was altered from primarily local with adjuvant systemic therapy to systemic therapy only.

 


View larger version (92K):

[in a new window]
 
Fig. 3A. —30-year-old woman with axillary node-positive infiltrating ductal carcinoma of left breast and skeletal metastases (midthoracic spine) at initial presentation. Coronal image from baseline FDG PET confirmed disease in thoracic spine (arrow; maximum standard uptake value, 4.5).

 


View larger version (99K):

[in a new window]
 
Fig. 3B. —30-year-old woman with axillary node-positive infiltrating ductal carcinoma of left breast and skeletal metastases (midthoracic spine) at initial presentation. Coronal image from follow-up FDG PET, performed to evaluate response to systemic chemotherapy, shows complete resolution of uptake in spine. FDG PET findings supported decision to pursue consolidation radiation therapy in this patient. She has no evidence of disease 1 year after radiation.

 


View larger version (96K):

[in a new window]
 
Fig. 4A. —54-year-old woman with axillary node-positive infiltrating lobular carcinoma of right breast. Patient had been disease-free on systemic hormonal therapy until 6 years after initial diagnosis when tumor markers became elevated. Posterior projection of restaging bone scan shows multiple foci of radiotracer uptake in spine, pelvis, and right rib, consistent with metastatic disease.

 


View larger version (85K):

[in a new window]
 
Fig. 4B. —54-year-old woman with axillary node-positive infiltrating lobular carcinoma of right breast. Patient had been disease-free on systemic hormonal therapy until 6 years after initial diagnosis when tumor markers became elevated. Posterior coronal image from FDG PET shows no increased uptake at corresponding skeletal sites. Activity in paraspinal regions is due to muscular uptake. Because of newly diagnosed skeletal recurrence, patient was started on systemic chemotherapy.

 

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the American Roentgen Ray Society.