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Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET

PURPOSE: We investigated the potential of interim 4′-[methyl-(11)C]thiothymidine ([(11)C]4DST) PET for predicting the chemoradiotherapeutic response for head and neck squamous cell carcinoma (HNSCC), in comparison with 2-deoxy-2-[(18)F]fluoro-D-glucose ([(18)F]FDG) PET. METHODS: A total of 32 patien...

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Autores principales: Mitamura, Katsuya, Norikane, Takashi, Yamamoto, Yuka, Fujimoto, Kengo, Takami, Yasukage, Hoshikawa, Hiroshi, Toyohara, Jun, Nishiyama, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876213/
https://www.ncbi.nlm.nih.gov/pubmed/33566186
http://dx.doi.org/10.1186/s13550-021-00749-y
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author Mitamura, Katsuya
Norikane, Takashi
Yamamoto, Yuka
Fujimoto, Kengo
Takami, Yasukage
Hoshikawa, Hiroshi
Toyohara, Jun
Nishiyama, Yoshihiro
author_facet Mitamura, Katsuya
Norikane, Takashi
Yamamoto, Yuka
Fujimoto, Kengo
Takami, Yasukage
Hoshikawa, Hiroshi
Toyohara, Jun
Nishiyama, Yoshihiro
author_sort Mitamura, Katsuya
collection PubMed
description PURPOSE: We investigated the potential of interim 4′-[methyl-(11)C]thiothymidine ([(11)C]4DST) PET for predicting the chemoradiotherapeutic response for head and neck squamous cell carcinoma (HNSCC), in comparison with 2-deoxy-2-[(18)F]fluoro-D-glucose ([(18)F]FDG) PET. METHODS: A total of 32 patients with HNSCC who underwent both [(11)C]4DST and [(18)F]FDG PET/CT before therapy (baseline) and at approximately 40 Gy point during chemoradiotherapy (interim) were available for a retrospective analysis of prospectively collected data. The baseline was treatment-naïve PET/CT scan as part of staging. The maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV) from [(18)F]FDG PET or proliferative tumor volume (PTV) from [(11)C]4DST PET, and total lesion glycolysis (TLG) from [(18)F]FDG PET or total lesion proliferation (TLP) from [(11)C]4DST PET were measured. MTV or PTV was defined as the volume with an SUVmax greater than 2.5. The differences in SUVmax (ΔSUVmax), MTV (ΔMTV) or PTV (ΔPTV) and TLG (ΔTLG) or TLP (ΔTLP) from baseline to interim PET scans were calculated. Patients without or with evidence of residual or recurrent disease at 3 months after completion of chemoradiotherapy were classified as showing a complete response (CR) and non-CR, respectively. RESULTS: All patients showed increased uptake in primary tumor on baseline [(11)C]4DST and [(18)F]FDG PET studies. All patients showed increased uptake on interim [(18)F]FDG PET, whereas 18 patients showed no increased uptake on interim [(11)C]4DST PET. After chemoradiotherapy, 25 patients were found to be in CR group and 7 to be in non-CR group. [(11)C]4DST ΔSUVmax, ΔPTV, and ΔTLP for CR group showed significantly greater reductions than the corresponding values for non-CR group (P = 0.044, < 0.001, < 0.001, respectively). However, there were no significant differences in [(18)F]FDG ΔSUVmax, ΔMTV, or ΔTLG between CR group and non-CR group. [(11)C]4DST ΔMTV of -90 was the best cutoff value for the early identification of patients with non-CR. CONCLUSION: These preliminary results suggest that interim [(11)C]4DST PET might be useful for predicting the chemoradiotherapeutic response in patients with HNSCC, in comparison with [(18)F]FDG PET.
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spelling pubmed-78762132021-02-24 Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET Mitamura, Katsuya Norikane, Takashi Yamamoto, Yuka Fujimoto, Kengo Takami, Yasukage Hoshikawa, Hiroshi Toyohara, Jun Nishiyama, Yoshihiro EJNMMI Res Original Research PURPOSE: We investigated the potential of interim 4′-[methyl-(11)C]thiothymidine ([(11)C]4DST) PET for predicting the chemoradiotherapeutic response for head and neck squamous cell carcinoma (HNSCC), in comparison with 2-deoxy-2-[(18)F]fluoro-D-glucose ([(18)F]FDG) PET. METHODS: A total of 32 patients with HNSCC who underwent both [(11)C]4DST and [(18)F]FDG PET/CT before therapy (baseline) and at approximately 40 Gy point during chemoradiotherapy (interim) were available for a retrospective analysis of prospectively collected data. The baseline was treatment-naïve PET/CT scan as part of staging. The maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV) from [(18)F]FDG PET or proliferative tumor volume (PTV) from [(11)C]4DST PET, and total lesion glycolysis (TLG) from [(18)F]FDG PET or total lesion proliferation (TLP) from [(11)C]4DST PET were measured. MTV or PTV was defined as the volume with an SUVmax greater than 2.5. The differences in SUVmax (ΔSUVmax), MTV (ΔMTV) or PTV (ΔPTV) and TLG (ΔTLG) or TLP (ΔTLP) from baseline to interim PET scans were calculated. Patients without or with evidence of residual or recurrent disease at 3 months after completion of chemoradiotherapy were classified as showing a complete response (CR) and non-CR, respectively. RESULTS: All patients showed increased uptake in primary tumor on baseline [(11)C]4DST and [(18)F]FDG PET studies. All patients showed increased uptake on interim [(18)F]FDG PET, whereas 18 patients showed no increased uptake on interim [(11)C]4DST PET. After chemoradiotherapy, 25 patients were found to be in CR group and 7 to be in non-CR group. [(11)C]4DST ΔSUVmax, ΔPTV, and ΔTLP for CR group showed significantly greater reductions than the corresponding values for non-CR group (P = 0.044, < 0.001, < 0.001, respectively). However, there were no significant differences in [(18)F]FDG ΔSUVmax, ΔMTV, or ΔTLG between CR group and non-CR group. [(11)C]4DST ΔMTV of -90 was the best cutoff value for the early identification of patients with non-CR. CONCLUSION: These preliminary results suggest that interim [(11)C]4DST PET might be useful for predicting the chemoradiotherapeutic response in patients with HNSCC, in comparison with [(18)F]FDG PET. Springer Berlin Heidelberg 2021-02-10 /pmc/articles/PMC7876213/ /pubmed/33566186 http://dx.doi.org/10.1186/s13550-021-00749-y Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Research
Mitamura, Katsuya
Norikane, Takashi
Yamamoto, Yuka
Fujimoto, Kengo
Takami, Yasukage
Hoshikawa, Hiroshi
Toyohara, Jun
Nishiyama, Yoshihiro
Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET
title Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET
title_full Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET
title_fullStr Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET
title_full_unstemmed Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET
title_short Interim 4′-[methyl-(11)C]-thiothymidine PET for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)F]FDG PET
title_sort interim 4′-[methyl-(11)c]-thiothymidine pet for predicting the chemoradiotherapeutic response in head and neck squamous cell carcinoma: comparison with [(18)f]fdg pet
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876213/
https://www.ncbi.nlm.nih.gov/pubmed/33566186
http://dx.doi.org/10.1186/s13550-021-00749-y
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