18 F-FLT PET/CT as an imaging tool for early prediction of pathological response in patients with locally advanced breast cancer treated with neoadjuvant chemotherapy: a pilot study

Purpose We evaluated whether 18 F-3′-deoxy-3′-fluorothymidine positron emission tomography (FLT PET) can predict the final postoperative histopathological response in primary breast cancer after the first cycle of neoadjuvant chemotherapy (NCT). Methods In this prospective cohort study of 15 patients with locally advanced operable breast cancer, FLT PET evaluations were performed before NCT, after the first cycle of NCT, and at the end of NCT. All patients subsequently underwent surgery. Variables from FLT PET examinations were correlated with postoperative histopathological results. Results At baseline, median of maximum standardized uptake values (SUV max ) in the groups showing a complete pathological response (pCR) + residual cancer burden (RCB) I, RCB II or RCB III did not differ significantly for the primary tumour (5.0 vs. 2.9 vs. 8.9, p = 0.293) or for axillary nodes (7.9 vs. 1.6 vs. 7.0, p = 0.363), whereas the Spearman correlation between SUV max and Ki67 proliferation rate index was significant ( r = 0.69, p < 0.001). Analysis of the relative percentage change of SUV max in the primary tumour (∆SUVT max ( t 1 )) and axillary nodes (∆SUVN max ( t 1 )) after the first NCT cycle showed that the power of ∆SUVT max ( t 1 ) to predict pCR + RCB I responses (AUC = 0.91, p < 0.001) was statistically significant, whereas ∆SUVN max ( t 1 ) had a moderate ability (AUC = 0.77, p = 0.119) to separate subjects with ΔSUVT max ( t 1 ) > −52.9 % into two groups: RCB III patients and a heterogeneous group that included RCB I and RCB II patients. A predictive score μ based on ΔSUVT max ( t 1 ) and ΔSUVN max ( t 1 ) parameters is proposed. Conclusion The preliminary findings of the present study suggest the potential utility of FLT PET scans for early monitoring of response to NCT and to formulate a therapeutic strategy consistent with the estimated efficacy of NCT. However, these results in a small patient population need to be validated in a larger independent cohort.