Cardiac Metabolic Changes on FDG-PET after Thoracic Chemoradiation Predict for Dose-response in Esophageal Cancer Patients

Author(s):  
S.J. Zakem ◽  
B.L. Jones ◽  
M. Miften ◽  
T. Schefter ◽  
C.G. Rusthoven ◽  
...  
2021 ◽  
Vol 20 ◽  
pp. 153303382110246
Author(s):  
Seokmo Lee ◽  
Yunseon Choi ◽  
Geumju Park ◽  
Sunmi Jo ◽  
Sun Seong Lee ◽  
...  

Background and Aims: This study evaluated the prognostic value of 18F-fluorodeoxyglucose positron emission tomography with integrated computed tomography (18F-FDG PET/CT) performed before and after concurrent chemoradiotherapy (CCRT) in esophageal cancer. Methods: We analyzed the prognosis of 50 non-metastatic squamous cell esophageal cancer (T1-4N0-2) patients who underwent CCRT with curative intent at Inje University Busan Paik Hospital and Haeundae Paik Hospital from 2009 to 2019. Median total radiation dose was 54 Gy (range 34-66 Gy). Our aim was to investigate the relationship between PET/CT values and prognosis. The primary end point was progression-free survival (PFS). Results: The median follow-up period was 9.9 months (range 1.7-85.7). Median baseline maximum standard uptake value (SUVmax) was 14.2 (range 3.2-27.7). After treatment, 29 patients (58%) showed disease progression. The 3-year PFS and overall survival (OS) were 24.2% and 54.5%, respectively. PFS was significantly lower ( P = 0.015) when SUVmax of initial PET/CT exceeded 10 (n = 22). However, OS did not reach a significant difference based on maximum SUV ( P = 0.282). Small metabolic tumor volume (≤14.1) was related with good PFS ( P = 0.002) and OS ( P = 0.001). Small total lesion of glycolysis (≤107.3) also had a significant good prognostic effect on PFS ( P = 0.009) and OS ( P = 0.025). In a subgroup analysis of 18 patients with follow-up PET/CT, the patients with SUV max ≤3.5 in follow-up PET/CT showed longer PFS ( P = 0.028) than those with a maximum SUV >3.5. Conclusion: Maximum SUV of PET/CT is useful in predicting prognosis of esophageal cancer patients treated with CCRT. Efforts to find more effective treatments for patients at high risk of progression are still warranted.


2012 ◽  
Vol 51 (5) ◽  
pp. 645-652 ◽  
Author(s):  
Shuichiro Nakaminato ◽  
Akira Toriihara ◽  
Tomoko Makino ◽  
Tatsuyuki Kawano ◽  
Seiji Kishimoto ◽  
...  

2012 ◽  
Vol 3 (4) ◽  
pp. 330-344 ◽  
Author(s):  
J. M. T. Omloo ◽  
M. van Heijl ◽  
O. S. Hoekstra ◽  
M. I. van Berge Henegouwen ◽  
J. J. B. van Lanschot ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (11) ◽  
pp. e0133690 ◽  
Author(s):  
Maarten C. J. Anderegg ◽  
Elisabeth J. de Groof ◽  
Suzanne S. Gisbertz ◽  
Roel J. Bennink ◽  
Sjoerd M. Lagarde ◽  
...  

2014 ◽  
Vol 23 (1) ◽  
pp. 12-15 ◽  
Author(s):  
Çiğdem Soydal ◽  
Cabir Büte Yüksel ◽  
Özlem N. Küçük ◽  
İlker Ökten ◽  
Elgin Özkan ◽  
...  

2004 ◽  
Vol 22 (14_suppl) ◽  
pp. 4055-4055 ◽  
Author(s):  
C. P. Duong ◽  
R. J. Hicks ◽  
L. Weih ◽  
A. Thompson ◽  
E. Drummond ◽  
...  

2004 ◽  
Vol 22 (14_suppl) ◽  
pp. 4055-4055
Author(s):  
C. P. Duong ◽  
R. J. Hicks ◽  
L. Weih ◽  
A. Thompson ◽  
E. Drummond ◽  
...  

2019 ◽  
Vol 21 (9) ◽  
pp. 1159-1167
Author(s):  
E. Jimenez-Jimenez ◽  
P. Mateos ◽  
I. Ortiz ◽  
N. Aymar ◽  
R. Roncero ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document