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Rivista di Medicina Nucleare e Imaging Molecolare

A Journal on Nuclear Medicine and Molecular Imaging
Affiliated to the Society of Radiopharmaceutical Sciences and to the International Research Group of Immunoscintigraphy
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The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2014 Dec 12

lingua: Inglese

Staging of locally advanced breast cancer and the prediction of response to neoadjuvant chemotherapy: complementary role of scintimammography and 18F-FDG PET/CT

Evangelista L. 1, Cervino A. R. 1, Michieletto S. 2, Saibene T. 2, Orvieto E. 3, Bozza F. 2, Ghiotto C. 4

1 Radiotherapy and Nuclear Medicine Unit, Oncological Institute of Veneto IOV, IRCCS, Padua, Italy;
2 Breast Unit, Oncological Institute of Veneto IOV, IRCCS, Padua, Italy;
3 Department of Pathology, University Hospital of Padua, Padua, Italy;
4 Medical Oncology 2 Unit, Oncological Institute of Veneto IOV, IRCCS, Padua, Italy


INTRODUCTION: The primary end-­point of the study was to established the role of sestamibi scintimammography and PET/CT findings in locally advanced breast cancer (LABC) before neoadjuvant systemic therapy (NST) in different histological subtypes. The secondary end-­point was to determine the role of FDG PET/CT as multi drug resistance marker.
METHODS: From January 2012, we prospectively enrolled 51 consecutive women (median age: 49 years; range: 27-­76 yrs) with a biopsy-­proven LABC. All patients underwent both sestamibi scintimammography and FDG PET/CT within one week before to start NST. Both examinations were qualitatively and semiquantitatively analysed. For scintimammography we calculated the tumor to background ratio (T/B) and the most intense uptake of the tumor to background ratio (I/B) according the following formula: T/B=[cntsT-­cntsB]/ [cntsB] and I/B [cntsI-­cntsB]/ [cntsB]. Furthermore, the percentage washout index (WO) for T and I were obtained, according to: WOT,I= [cntsT,I]early image-­[cntsT,I]delayed image/[cntsT,I]early image. Maximum and average (avg) standardized uptake value (SUV) was computed by PET/CT, using a region of interest. Patients who had an evidence of systemic metastases or a second active cancer at imaging scans, were excluded. At the end of pre-­operative therapy, the response to therapy was assessed by the analysis of surgical specimen and then correlated with both scintimammographic and PET/CT data.
RESULTS: Based on the inclusion criteria, the final analysis was performed in 49 patients. Scintimammography and PET/CT showed a sensitivity of 100% for the evaluation of primary cancer, while PET/CT showed a slightly higher detection rate for axillary lymph node than scintimammography. According to the biological pattern, SUVmax and SUVavg resulted significantly different among histological subtypes, whereas scintimammographic data did not. At the end of neo-­adjuvant therapy, pathological complete response was obtained in 12 (24.4%) patients, while 37 had a partial or no response to NST (identified as no-­responders). On the basis of histopathological response to NST, median WOI resulted significantly lower in responders than no-­responders, (30.5 vs. 44%; p=0.027). Conversely, SUVmax and SUVavg were significantly higher in responders than no-­responders (all p<0.05). In this latter subset of patients, high WOTs were associated with low SUVs. On the contrary, in responder group, high SUVs were reported particularly for high WOT values.
CONCLUSIONS: Scintimammography with sestamibi did not accurately determine the responsiveness to therapy. FDG PET/CT is more accurate in the prediction of response to therapy, particularly in the aggressive LABC subtype. Moreover, semiquantitative data by FDG PET seems to be linked with the chemosensitivity to NST.

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