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Positron emission tomography/computed tomography imaging in Merkel cell carcinoma: A study of 270 scans in 97 patients at the Dana-Farber/Brigham and Women's Cancer Center - 21/03/13

Doi : 10.1016/j.jaad.2012.08.042 
Elena B. Hawryluk, MD, PhD a, Kevin N. O'Regan, MB, FFRRCSI b, Niall Sheehy, MB, FFRRCSI b, Ye Guo, MSc c, Andrew Dorosario, BA d, Christopher G. Sakellis, MD b, Heather A. Jacene, MD b, Linda C. Wang, MD, JD c, d,
a Department of Dermatology, Harvard Medical School, Boston, Massachusetts 
b Department of Imaging, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, Massachusetts 
c Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 
d Center for Cutaneous Oncology, Dana-Farber/Brigham and Women's Cancer Center, Harvard Medical School, Boston, Massachusetts 

Reprint requests: Linda C. Wang, MD, JD, Institute for Cancer Care at Mercy Medical Center, 301 St Paul Pl, McAuley POB, Suite 607, Baltimore, MD 21202.

Abstract

Background

Merkel cell carcinoma (MCC) is a rare and lethal cutaneous neuroendocrine carcinoma. Imaging is crucial for accurate staging, which remains a strong predictor of survival, as well as earlier detection of recurrence and progression, which are common despite aggressive management. There is no consensus on the role of initial and subsequent imaging for MCC.

Objective

We sought to evaluate the use of 2-fluoro-[18F]-deoxy-2-D-glucose (FDG)-positron emission tomography (PET)/computed tomography (CT) in the management of MCC.

Methods

In all, 270 FDG-PET/CT studies were performed in 97 patients with pathology-proven MCC at the Dana-Farber/Brigham and Women's Cancer Center, Boston, Mass, from August 2003 to December 2010.

Results

FDG-PET/CT scans were obtained as part of the initial (61 scans in 61 patients) and subsequent (209 scans in 79 patients) treatment strategies. MCCs were FDG-avid with a mean maximum standardized uptake value of primary lesions of 6.5 (range 1.3-12.9) and a mean maximum standardized uptake value of regional and distant metastases of 7.2 (range 1.5-9.9). FDG-PET/CT upstaged 16% of patients who underwent baseline scans. FDG-PET/CT studies showed that bone and bone-marrow metastases were more common than previously reported, and were often undetected by CT.

Limitations

Our study is limited by its retrospective design, and potential referral bias associated with a tertiary care center.

Conclusions

FDG-PET/CT performed as part of the initial management strategy tended to upstage patients with more advanced disease. FDG-PET/CT performed as part of the subsequent treatment strategy identified metastatic disease, particularly in bone/bone marrow, which was not seen on CT. FDG-PET/CT imaging is a valuable staging and restaging tool in MCC management.

Le texte complet de cet article est disponible en PDF.

Key words : computed tomography, 2-fluoro-[18F]-deoxy-2-D-glucose, imaging, Merkel cell carcinoma, metastasis, positron emission tomography, staging

Abbreviations used : AJCC, CT, DF/BWCC, FDG, MCC, MRI, PET, SLNB, SUVmax, 18F


Plan


 Dr O'Regan is currently affiliated with the Department of Radiology, Cork University Hospital, Cork, Ireland; Dr Sheehy is currently affiliated with Department of Radiology, St James's Hospital, Dublin, Ireland; and Dr Wang is currently affiliated with the Institute for Cancer Care at Mercy Medical Center, Baltimore, Maryland.
 Funding sources: None.
 Conflicts of interest: None declared.


© 2012  American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
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