Whole‐body [18F]fluoro‐2‐deoxyglucose positron emission tomography scan staging prior to planned radical hysterectomy and pelvic lymphadenectomy
. Unger JB, Ivy JJ, Ramaswamy MR, Charrier A, Connor P. Whole‐body [18F]fluoro‐2‐deoxyglucose positron emission tomography scan staging prior to planned radical hysterectomy and pelvic lymphadenectomy. Int J Gynecol Cancer 2005;15:1060–1064. The aim of the study was to determine the effectiveness o...
Gespeichert in:
Veröffentlicht in: | International journal of gynecological cancer 2005-11, Vol.15 (6), p.1060-1064 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | . Unger JB, Ivy JJ, Ramaswamy MR, Charrier A, Connor P. Whole‐body [18F]fluoro‐2‐deoxyglucose positron emission tomography scan staging prior to planned radical hysterectomy and pelvic lymphadenectomy. Int J Gynecol Cancer 2005;15:1060–1064.
The aim of the study was to determine the effectiveness of whole‐body [18F]fluoro‐2‐deoxyglucose positron emission tomography (FDG PET) imaging in properly selecting candidates for radical hysterectomy who are at low risk for subsequent chemoradiation. Retrospective study of 14 women undergoing planned radical hysterectomy and pelvic lymphadenectomy with clinically localized cervical cancer and either negative or inconclusive metastatic nodal disease by PET scan was performed. Pelvic lymph nodes were clearly negative by FDG PET scan in 12 of the 14 women. Two women had focal FDG uptake suspicious, although not definitive, for nodal metastasis, and pelvic nodes were positive at surgery in both. Computed tomography (CT) scan failed to detect nodal disease in either woman. Neither PET nor CT was effective at detecting parametrial disease, and both also failed to detect the primary tumor in some cases. Women with FDG PET scans that are clearly negative for nodal disease are good candidates for radical hysterectomy and are at low risk for subsequent chemoradiation. |
---|---|
ISSN: | 1048-891X 1525-1438 |
DOI: | 10.1111/j.1525-1438.2005.00262.x |