Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Jun;9(12):4059-4068.
doi: 10.1002/cam4.3044. Epub 2020 Apr 12.

Usefulness of 18 F-fluorodeoxyglucose positron emission tomography/computed tomography for predicting the prognosis and treatment response of neoadjuvant therapy for pancreatic ductal adenocarcinoma

Affiliations

Usefulness of 18 F-fluorodeoxyglucose positron emission tomography/computed tomography for predicting the prognosis and treatment response of neoadjuvant therapy for pancreatic ductal adenocarcinoma

Takahiro Yokose et al. Cancer Med. 2020 Jun.

Abstract

Background: The Response Evaluation Criteria in Solid Tumors (RECIST) for computed tomography (CT) is preoperatively used to evaluate therapeutic effects. However, it does not reflect the pathological treatment response (PTR) of pancreatic ductal adenocarcinoma (PDAC). The Positron Emission Tomography Response Criteria in Solid Tumors (PERCIST) for positron emission tomography (PET)/CT is effective in other cancers. This study aimed to confirm the usefulness of PERCIST and the prognostic utility of PET/CT for PDAC.

Methods: Forty-two consecutive patients with PDAC who underwent neoadjuvant therapy (NAT) and pancreatectomy at our institution between 2014 and 2018 were retrospectively analyzed. We evaluated the treatment response and prognostic significance of PET/CT parameters and other clinicopathological factors.

Results: Twenty-two patients who underwent PET/CT both before and after NAT with the same protocol were included. RECIST revealed stable disease and partial response in 20 and 2 cases, respectively. PERCIST revealed stable metabolic disease, partial metabolic response, and complete metabolic response in 8, 9, and 5 cases, respectively. The PTR was G3, G2, and G1 in 8, 12, and 2 cases, respectively. For comparing the concordance rates between PTR and each parameter, PERCIST (72.7% [16/22]) was significantly superior to RECIST (36.4% [8/22]) (P = .017). The area under the curve survival values of PET/CT parameters were 0.777 for metabolic tumor volume (MTV), 0.500 for maximum standardized uptake value, 0.554 for peak standardized uptake value corrected for lean body mass, and 0.634 for total lesion glycolysis. A 50% cut-off value for the MTV reduction rate yielded the largest difference in survival between responders and nonresponders. On multivariate analysis, MTV reduction rates < 50% were independent predictors for relapse-free survival (hazard ratio [HR], 3.92; P = .044) and overall survival (HR, 14.08; P = .023).

Conclusions: PERCIST was more accurate in determining NAT's therapeutic effects for PDAC than RECIST. MTV reduction rates were independent prognostic factors for PDAC.

Keywords: MTV; PERCIST; PET/CT; pancreatic ductal adenocarcinoma.

PubMed Disclaimer

Conflict of interest statement

Masahiro Shinoda reports grants from Taiho Pharmaceutical Co., Ltd., Shionogi Co., Ltd., Eisai Co., Ltd., Novartis Pharma KK, Asahi KASEI Co., Ltd., Daiichi Sankyo Co., Ltd., outside the submitted work; Ryota Ishii reports personal fees from Kowa Company, Ltd., outside the submitted work; Shigeo Okuda reports grants from AZE Co., Ltd., outside the submitted work; Yuko Kitagawa reports grants from Taiho Pharmaceutical Co., Ltd., Chugai Pharmaceutical Co., Ltd., Yakult Honsha Co., Ltd., Daiichi Sankyo Co., Ltd., Merck Serono Co., Ltd., Asahi KASEI Co., Ltd., EA Pharma Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Otsuka Pharmaceutical Factory Inc, Shionogi Co., Ltd., Kaken Pharmaceutical Co., LTD., Kowa Pharmaceutical Co., Ltd., Astellas Pharma Inc, Medicon Inc, Dainippon Sumitomo Pharma Co., Ltd., Taisho Toyama Pharmaceutical Co., Ltd., Kyouwa Hakkou Kirin Co., Ltd., Pfizer Japan Inc, Ono Pharmaceutical CO., LTD., Nihon Pharmaceutical CO., LTD., Japan Blood Products Organization, Medtronic Japan Co., Ltd., Sanofi KK, Eisai Co., Ltd., Tsumura Co., KCI Licensing, Inc, Abbott Japan CO., LTD., Fujifilm Toyama Chemical Co., Ltd., outside the submitted work. Other authors have nothing to disclose.

Figures

Figure 1
Figure 1
Representative FDG PET/CT examination before and after neoadjuvant therapy (NAT) revealed a significant decrease in FDG uptake in the tumor (arrow)
Figure 2
Figure 2
Waterfall plot analysis for the reduction rate of each parameter: tumor size, maximum standardized uptake value (SUVmax), and peak standardized uptake value corrected for lean body mass (SULpeak)
Figure 3
Figure 3
Analysis of receiver operating characteristic (ROC) curves to determine the best indicator for predicting the pathological treatment responders. The area under the ROC curve (AUC) values for the reduction rate of tumor size, maximum standardized uptake value (SUVmax), peak standardized uptake value corrected for lean body mass (SULpeak), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were 0.478, 0.723, 0.786, 0.576, and 0.661, respectively
Figure 4
Figure 4
Analysis of receiver operating characteristic (ROC) curve to determine the best indicator for predicting recurrence (A) and prognosis (B). For recurrence, the area under the ROC curve (AUC) values for the reduction rate of tumor size, maximum standardized uptake value (SUVmax), peak standardized uptake value corrected for lean body mass (SULpeak), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were 0.678, 0.463, 0.558, 0.793, and 0.669, respectively. For survival, the AUC values for reduction rate of tumor size, SUVmax, SULpeak, MTV, and TLG were 0.643, 0.500, 0.554, 0.777, and 0.634, respectively
Figure 5
Figure 5
Survival curve using the Kaplan‐Meier method. A, The relapse‐free survival curve of patients with the metabolic tumor volume (MTV) reduction rate with a 50% cut‐off value. B, Overall survival curve of patients with the MTV reduction rate with a 50% cut‐off value

Similar articles

Cited by

References

    1. Sant M, Allemani C, Santaquilani M, Knijn A, Marchesi F, Capocaccia R. EUROCARE‐4. survival of cancer patients diagnosed in 1995–1999. Results and commentary. Eur J Cancer. 2009;45:931‐991. - PubMed
    1. Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127:2893‐2917. - PubMed
    1. Tempero MA, Malafa MP, Al‐Hawary M, et al. Pancreatic adenocarcinoma, Version 2.2017, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 2017;15:1028‐1061. - PubMed
    1. Uesaka K, Boku N, Fukutomi A, et al. Adjuvant chemotherapy of S‐1 versus gemcitabine for resected pancreatic cancer: a phase 3, open‐label, randomised, non‐inferiority trial (JASPAC 01). Lancet. 2016;388:248‐257. - PubMed
    1. Mellon EA, Strom TJ, Hoffe SE, et al. Favorable perioperative outcomes after resection of borderline resectable pancreatic cancer treated with neoadjuvant stereotactic radiation and chemotherapy compared with upfront pancreatectomy for resectable cancer. J Gastrointest Oncol. 2016;7:547‐555. - PMC - PubMed

MeSH terms

Substances