http://www.cnr.it/ontology/cnr/individuo/prodotto/ID188617
Role of FDG-PET in the management of gestational trophoblastic neoplasia (GTN) (Abstract in rivista)
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- Label
- Role of FDG-PET in the management of gestational trophoblastic neoplasia (GTN) (Abstract in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Alternative label
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- Paola Mapelli; Maria Picchio; Elena Spinapolice; Giorgia Mangili; Margarita Kirienko; Cinzia Gentile; Elisabetta Garavaglia; Veronica Giorgione; Luigi Gianolli; Cristina Messa. (literal)
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- University of Milano-Bicocca, Milan, Italy. Nuclear Medicine Unit, Scientific Institute San Raffaele, Milan, Italy. IBFM-CNR, Milan, Italy. Gynecology and Obstetrics Unit, Scientific Institute San Raffaele, Milan, Italy. Nuclear Medicine Unit, San Gerardo Hospital, Monza, Italy. Tecnomed Foundation, University of Milano-Bicocca, Milan, Italy. (literal)
- Titolo
- Role of FDG-PET in the management of gestational trophoblastic neoplasia (GTN) (literal)
- Abstract
- Objectives: To evaluate the role of FDG-PET and PET/CT in staging, monitoring treatment efficacy and impact on patients management in GTN patients.
Methods: 38 patients referred to our institution for GTN treatment between 2004 and 2011 were retrospectively enrolled. During staging all patients underwent to ?HCG measurements, trans-vaginal ultrasound(TV-US), Chest X-ray, whole-body CT and PET/CT (n= 32) or PET (n= 6). 8 patients with positive extra-uterine PET/CT basal study were re-evaluated by a second PET/CT after ?HCG normalization. PET(n=1) or PET/CT(n=3) were repeated in patients with ?HCG resistance. TV-US and whole-body CT were used as standard of reference.
Results: Staging: PET or PET/CT correctly identified uterine disease in 22/25 patients(88%), lung metastases in 12/19(63%) patients, lymphnodal involvement in 2/2 patients, ovarian metastases in 1/1, pancreatic metastases in 1/1 and liver metastases in 2/4(50%) patients. Restaging: in 8/8 patients with extra-uterine disease during staging, PET/CT documented complete response to therapy after ?HCG normalization. PET and PET/CT identified the sites of persistent disease in all ?HCG resistance patients (n=4), leading to tailored treatment: 2/4 patients underwent to second line chemotherapy and in 2/4 patients surgical removal of resistant disease (lung and uterus) was performed.
Conclusions: During staging of GTN, PET has low sensitivity and high specificity. During treatment monitoring PET may detect a complete response to chemotherapy earlier than CT. In patients with resistant disease to chemotherapy PET may play a role in changing management and guiding treatment (literal)
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