Prediction of response to neoadjuvant chemotherapy in osteosarcoma using dual-phase super(18)F-FDG PET/CT

Objectives: We evaluated the ability of dual-phase super(18)F-FDG PET/CT to predict the histological response after neoadjuvant chemotherapy (NAC) in osteosarcoma. Methods: Thirty-one patients with osteosarcoma treated with NAC and surgery were prospectively enrolled. After injection of super(18)F-F...

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Veröffentlicht in:European radiology 2015-07, Vol.25 (7), p.2015-2024
Hauptverfasser: Byun, Byung Hyun, Kim, Sung Hoon, Lim, Sang Moo, Lim, Ilhan, Kong, Chang-Bae, Song, Won Seok, Cho, Wan Hyeong, Jeon, Dae-Geun, Lee, Soo-Yong, Koh, Jae-Soo, Chung, Soo Kyo
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container_end_page 2024
container_issue 7
container_start_page 2015
container_title European radiology
container_volume 25
creator Byun, Byung Hyun
Kim, Sung Hoon
Lim, Sang Moo
Lim, Ilhan
Kong, Chang-Bae
Song, Won Seok
Cho, Wan Hyeong
Jeon, Dae-Geun
Lee, Soo-Yong
Koh, Jae-Soo
Chung, Soo Kyo
description Objectives: We evaluated the ability of dual-phase super(18)F-FDG PET/CT to predict the histological response after neoadjuvant chemotherapy (NAC) in osteosarcoma. Methods: Thirty-one patients with osteosarcoma treated with NAC and surgery were prospectively enrolled. After injection of super(18)F-FDG, both early (~60 min) and delayed (~150 min) PET were acquired before and after the completion of NAC. SUVmax, early/delayed SUVmax change (RImax), and early/delayed SUVmean change (RImean) of tumour were measured before (SUV1, RImax1, and RImean1) and after NAC (SUV2, RImax2, and RImean2). Then, we calculated the percentage changes between SUV1 and SUV2 (%SUV). Results: Twelve patients (39 %) exhibited good histological response after NAC. SUVmax, RImax, and RImean significantly decreased after NAC. Before NAC, only RImean1 predicted good histological response with the optimal criterion of < 10 %, sensitivity of 92 %, specificity of 57 %, and accuracy of 71 %. After NAC, %SUV, SUV2, and RImax2 predicted histological response. By using combined criterion of %SUV and RImax2 or SUV2 and RImean1 or SUV2 and RImax2, accuracies were 81 %, 77 %, and 77 %, respectively. Conclusions: The histological response after NAC could be predicted by using RImean1 before the initiation of NAC in osteosarcoma. The combined use of SUV and RI values may provide a better prediction. Key Points : times Pretreatment dual-phase FDG-PET was useful to predict histological response in osteosarcoma. times A combination of early and delayed PET may increase the predictive value. times Early/delayed SUV change of tumours significantly decreased after neoadjuvant chemotherapy.
doi_str_mv 10.1007/s00330-015-3609-3
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Methods: Thirty-one patients with osteosarcoma treated with NAC and surgery were prospectively enrolled. After injection of super(18)F-FDG, both early (~60 min) and delayed (~150 min) PET were acquired before and after the completion of NAC. SUVmax, early/delayed SUVmax change (RImax), and early/delayed SUVmean change (RImean) of tumour were measured before (SUV1, RImax1, and RImean1) and after NAC (SUV2, RImax2, and RImean2). Then, we calculated the percentage changes between SUV1 and SUV2 (%SUV). Results: Twelve patients (39 %) exhibited good histological response after NAC. SUVmax, RImax, and RImean significantly decreased after NAC. Before NAC, only RImean1 predicted good histological response with the optimal criterion of &lt; 10 %, sensitivity of 92 %, specificity of 57 %, and accuracy of 71 %. After NAC, %SUV, SUV2, and RImax2 predicted histological response. By using combined criterion of %SUV and RImax2 or SUV2 and RImean1 or SUV2 and RImax2, accuracies were 81 %, 77 %, and 77 %, respectively. Conclusions: The histological response after NAC could be predicted by using RImean1 before the initiation of NAC in osteosarcoma. The combined use of SUV and RI values may provide a better prediction. 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Methods: Thirty-one patients with osteosarcoma treated with NAC and surgery were prospectively enrolled. After injection of super(18)F-FDG, both early (~60 min) and delayed (~150 min) PET were acquired before and after the completion of NAC. SUVmax, early/delayed SUVmax change (RImax), and early/delayed SUVmean change (RImean) of tumour were measured before (SUV1, RImax1, and RImean1) and after NAC (SUV2, RImax2, and RImean2). Then, we calculated the percentage changes between SUV1 and SUV2 (%SUV). Results: Twelve patients (39 %) exhibited good histological response after NAC. SUVmax, RImax, and RImean significantly decreased after NAC. Before NAC, only RImean1 predicted good histological response with the optimal criterion of &lt; 10 %, sensitivity of 92 %, specificity of 57 %, and accuracy of 71 %. After NAC, %SUV, SUV2, and RImax2 predicted histological response. By using combined criterion of %SUV and RImax2 or SUV2 and RImean1 or SUV2 and RImax2, accuracies were 81 %, 77 %, and 77 %, respectively. Conclusions: The histological response after NAC could be predicted by using RImean1 before the initiation of NAC in osteosarcoma. The combined use of SUV and RI values may provide a better prediction. 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Methods: Thirty-one patients with osteosarcoma treated with NAC and surgery were prospectively enrolled. After injection of super(18)F-FDG, both early (~60 min) and delayed (~150 min) PET were acquired before and after the completion of NAC. SUVmax, early/delayed SUVmax change (RImax), and early/delayed SUVmean change (RImean) of tumour were measured before (SUV1, RImax1, and RImean1) and after NAC (SUV2, RImax2, and RImean2). Then, we calculated the percentage changes between SUV1 and SUV2 (%SUV). Results: Twelve patients (39 %) exhibited good histological response after NAC. SUVmax, RImax, and RImean significantly decreased after NAC. Before NAC, only RImean1 predicted good histological response with the optimal criterion of &lt; 10 %, sensitivity of 92 %, specificity of 57 %, and accuracy of 71 %. After NAC, %SUV, SUV2, and RImax2 predicted histological response. By using combined criterion of %SUV and RImax2 or SUV2 and RImean1 or SUV2 and RImax2, accuracies were 81 %, 77 %, and 77 %, respectively. Conclusions: The histological response after NAC could be predicted by using RImean1 before the initiation of NAC in osteosarcoma. The combined use of SUV and RI values may provide a better prediction. Key Points : times Pretreatment dual-phase FDG-PET was useful to predict histological response in osteosarcoma. times A combination of early and delayed PET may increase the predictive value. times Early/delayed SUV change of tumours significantly decreased after neoadjuvant chemotherapy.</abstract><doi>10.1007/s00330-015-3609-3</doi></addata></record>
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title Prediction of response to neoadjuvant chemotherapy in osteosarcoma using dual-phase super(18)F-FDG PET/CT
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