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Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy

Neoadjuvant chemotherapy (NAC) has become a standard therapy for patients with advanced breast cancer. Pathological complete response (pCR) after NAC is an important prognostic indicator, but some patients with pCR continue to experience recurrence. So new predictive and prognostic markers in additi...

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Autores principales: Ishiba, Toshiyuki, Nakagawa, Tsuyoshi, Sato, Takanobu, Nagahara, Makoto, Oda, Goshi, Sugimoto, Hitoshi, Kasahara, Mai, Hosoya, Tokuko, Kubota, Kazunori, Fujioka, Tomoyuki, Danenberg, Peter, Danenberg, Kathleen, Uetake, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690821/
https://www.ncbi.nlm.nih.gov/pubmed/26722637
http://dx.doi.org/10.1186/s40064-015-1634-y
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author Ishiba, Toshiyuki
Nakagawa, Tsuyoshi
Sato, Takanobu
Nagahara, Makoto
Oda, Goshi
Sugimoto, Hitoshi
Kasahara, Mai
Hosoya, Tokuko
Kubota, Kazunori
Fujioka, Tomoyuki
Danenberg, Peter
Danenberg, Kathleen
Uetake, Hiroyuki
author_facet Ishiba, Toshiyuki
Nakagawa, Tsuyoshi
Sato, Takanobu
Nagahara, Makoto
Oda, Goshi
Sugimoto, Hitoshi
Kasahara, Mai
Hosoya, Tokuko
Kubota, Kazunori
Fujioka, Tomoyuki
Danenberg, Peter
Danenberg, Kathleen
Uetake, Hiroyuki
author_sort Ishiba, Toshiyuki
collection PubMed
description Neoadjuvant chemotherapy (NAC) has become a standard therapy for patients with advanced breast cancer. Pathological complete response (pCR) after NAC is an important prognostic indicator, but some patients with pCR continue to experience recurrence. So new predictive and prognostic markers in addition to pCR are needed following NAC for breast cancer. Fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) can evaluate metastases in the entire body simultaneously, and has several potential advantages over conventional imaging modalities. The purpose of this study was to evaluate whether FDG-PET/CT can determine NAC response and whether FDG-PET/CT can be a new prognostic marker. We imaged 83 breast cancer tumors with FDG-PET/CT, ultrasound (US), and magnetic resonance imaging (MRI) to evaluate NAC efficacy. As we previously analyzed 110 breast cancers with FDG PET/CT, we defined a threshold of >1.7 maximum standardized uptake value (SUV(max)) as abnormal fluorodeoxyglucose (FDG) uptake. After NAC, 16 (19.3 %) tumors had a complete response, 54 (65.1 %) had a partial response, 11 (13.3 %) showed stable disease, and 2 (2.4 %) showed progressive disease. One of the two patients with progressive disease had bone metastasis detected by FDG-PET/CT and was not operated on. Remote metastases were evident in 2.4 % of patients after NAC as determined by FDG-PET/CT. Overall, 17 patients had pathological complete response (pCR). The sensitivity of abnormal FDG uptake after NAC for non-pCR was 20.3 % and the specificity was 94.7 %. Patients with abnormal FDG uptake after NAC experienced significantly more recurrences (P = 0.004) and more of them died (P = 0.010). Moreover, the difference in disease-free survival was more significant in the estrogen receptor (ER)-negative group. FDG-PET after NAC may be more effective for predicting prognosis than for evaluating treatment response. This tendency was particularly remarkable in ER-negative breast cancer tumors. FDG-PET/CT is useful for reevaluating surgical applicability after NAC.
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spelling pubmed-46908212015-12-31 Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy Ishiba, Toshiyuki Nakagawa, Tsuyoshi Sato, Takanobu Nagahara, Makoto Oda, Goshi Sugimoto, Hitoshi Kasahara, Mai Hosoya, Tokuko Kubota, Kazunori Fujioka, Tomoyuki Danenberg, Peter Danenberg, Kathleen Uetake, Hiroyuki Springerplus Research Neoadjuvant chemotherapy (NAC) has become a standard therapy for patients with advanced breast cancer. Pathological complete response (pCR) after NAC is an important prognostic indicator, but some patients with pCR continue to experience recurrence. So new predictive and prognostic markers in addition to pCR are needed following NAC for breast cancer. Fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) can evaluate metastases in the entire body simultaneously, and has several potential advantages over conventional imaging modalities. The purpose of this study was to evaluate whether FDG-PET/CT can determine NAC response and whether FDG-PET/CT can be a new prognostic marker. We imaged 83 breast cancer tumors with FDG-PET/CT, ultrasound (US), and magnetic resonance imaging (MRI) to evaluate NAC efficacy. As we previously analyzed 110 breast cancers with FDG PET/CT, we defined a threshold of >1.7 maximum standardized uptake value (SUV(max)) as abnormal fluorodeoxyglucose (FDG) uptake. After NAC, 16 (19.3 %) tumors had a complete response, 54 (65.1 %) had a partial response, 11 (13.3 %) showed stable disease, and 2 (2.4 %) showed progressive disease. One of the two patients with progressive disease had bone metastasis detected by FDG-PET/CT and was not operated on. Remote metastases were evident in 2.4 % of patients after NAC as determined by FDG-PET/CT. Overall, 17 patients had pathological complete response (pCR). The sensitivity of abnormal FDG uptake after NAC for non-pCR was 20.3 % and the specificity was 94.7 %. Patients with abnormal FDG uptake after NAC experienced significantly more recurrences (P = 0.004) and more of them died (P = 0.010). Moreover, the difference in disease-free survival was more significant in the estrogen receptor (ER)-negative group. FDG-PET after NAC may be more effective for predicting prognosis than for evaluating treatment response. This tendency was particularly remarkable in ER-negative breast cancer tumors. FDG-PET/CT is useful for reevaluating surgical applicability after NAC. Springer International Publishing 2015-12-24 /pmc/articles/PMC4690821/ /pubmed/26722637 http://dx.doi.org/10.1186/s40064-015-1634-y Text en © Ishiba et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Ishiba, Toshiyuki
Nakagawa, Tsuyoshi
Sato, Takanobu
Nagahara, Makoto
Oda, Goshi
Sugimoto, Hitoshi
Kasahara, Mai
Hosoya, Tokuko
Kubota, Kazunori
Fujioka, Tomoyuki
Danenberg, Peter
Danenberg, Kathleen
Uetake, Hiroyuki
Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy
title Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy
title_full Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy
title_fullStr Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy
title_full_unstemmed Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy
title_short Efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy
title_sort efficiency of fluorodeoxyglucose positron emission tomography/computed tomography to predict prognosis in breast cancer patients received neoadjuvant chemotherapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690821/
https://www.ncbi.nlm.nih.gov/pubmed/26722637
http://dx.doi.org/10.1186/s40064-015-1634-y
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