Erschienen in:
17.09.2015 | Breast
Early prediction of response to neoadjuvant chemotherapy in breast cancer patients: comparison of single-voxel 1H-magnetic resonance spectroscopy and 18F-fluorodeoxyglucose positron emission tomography
verfasst von:
Nariya Cho, Seock-Ah Im, Keon Wook Kang, In-Ae Park, In Chan Song, Kyung-Hun Lee, Tae-Yong Kim, Hyunjong Lee, In Kook Chun, Hai-Jeon Yoon, Woo Kyung Moon
Erschienen in:
European Radiology
|
Ausgabe 7/2016
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Abstract
Objectives
To prospectively compare performances of single-voxel proton magnetic resonance spectroscopy (1H-MRS) and 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) in predicting pathologic response to neoadjuvant chemotherapy (NAC) in breast cancer patients.
Methods
Thirty-five breast cancer patients who received NAC and subsequent surgery were prospectively enrolled. MRS and FDG-PET were performed before and after the 1st NAC cycle. Percentage changes of total choline-containing compounds (tCho) via MRS, and maximum and peak standardized uptake values (SUVmax, SUVpeak) and total lesion glycolysis (TLG) via FDG-PET were measured, and their performances in predicting pathologic complete response (pCR) were compared.
Results
Of the 35 patients, 6 showed pCR and 29 showed non-pCR. Mean % reductions of tCho, SUVmax, SUVpeak, and TLG of the pCR group were larger than those of the non-pCR group (-80.3 ± 13.9 % vs. -32.1 ± 49.4 %, P = 0.025; -54.7 ± 22.1 % vs. -26.3 ± 33.7 %, P = 0.058; -60.7 ± 18.3 % vs. -32.3 ± 23.3 %, P = 0.009; -89.5 ± 8.5 % vs. -52.6 ± 36.2 %, P = 0.020). Diagnostic accuracy (area under ROC curve; Az, 0.911) of the % reduction of tCho was comparable to those of %SUVmax (0.822), SUVpeak (0.862), and TLG (0.879) in distinguishing pCR from non-pCR (all P > 0.05).
Conclusion
MRS showed comparable performance to FDG-PET in early prediction of pCR in breast cancer patients.
Key points
• MRS can predict response to NAC in breast cancer post-1
st
cycle.
• Changes in tCho and SUV after NAC reflect tumour cellularity changes.
• MRS can be an alternative to FDG-PET in predicting response to NAC.