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NEOadjuvant therapy monitoring with PET and CT in Esophageal Cancer (NEOPEC-trial).

Authors :
Heijl, M. van
Omloo, J.M.
Berge Henegouwen, M.I. van
Busch, O.R.
Tilanus, H.W.
Bossuyt, P.M.
Hoekstra, O.S.
Stoker, J.
Hulshof, M.C.C.
Gaast, A. van der
Nieuwenhuijzen, G.A.P
Bonenkamp, J.J.
Plukker, J.T.
Bilgen, E.J.
Kate, F.J. ten
Boellaard, R.
Pruim, J.
Sloof, G.W.
Lanschot, J.J. van
Heijl, M. van
Omloo, J.M.
Berge Henegouwen, M.I. van
Busch, O.R.
Tilanus, H.W.
Bossuyt, P.M.
Hoekstra, O.S.
Stoker, J.
Hulshof, M.C.C.
Gaast, A. van der
Nieuwenhuijzen, G.A.P
Bonenkamp, J.J.
Plukker, J.T.
Bilgen, E.J.
Kate, F.J. ten
Boellaard, R.
Pruim, J.
Sloof, G.W.
Lanschot, J.J. van
Source :
BMC Medical Physics; 3; 3; 1756-6649; 31-07-2008; vol. 8; ~BMC Medical Physics~3~3~~~1756-6649~31-07-2008~8~~
Publication Year :
2008

Abstract

Contains fulltext : 70883.pdf (publisher's version ) (Open Access)<br />BACKGROUND: Surgical resection is the preferred treatment of potentially curable esophageal cancer. To improve long term patient outcome, many institutes apply neoadjuvant chemoradiotherapy. In a large proportion of patients no response to chemoradiotherapy is achieved. These patients suffer from toxic and ineffective neoadjuvant treatment, while appropriate surgical therapy is delayed. For this reason a diagnostic test that allows for accurate prediction of tumor response early during chemoradiotherapy is of crucial importance. CT-scan and endoscopic ultrasound have limited accuracy in predicting histopathologic tumor response. Data suggest that metabolic changes in tumor tissue as measured by FDG-PET predict response better. This study aims to compare FDG-PET and CT-scan for the early prediction of non-response to preoperative chemoradiotherapy in patients with potentially curable esophageal cancer. METHODS/DESIGN: Prognostic accuracy study, embedded in a randomized multicenter Dutch trial comparing neoadjuvant chemoradiotherapy for 5 weeks followed by surgery versus surgery alone for esophageal cancer. This prognostic accuracy study is performed only in the neoadjuvant arm of the randomized trial. In 6 centers, 150 consecutive patients will be included over a 3 year period. FDG-PET and CT-scan will be performed before and 2 weeks after the start of the chemoradiotherapy. All patients complete the 5 weeks regimen of neoadjuvant chemoradiotherapy, regardless the test results. Pathological examination of the surgical resection specimen will be used as reference standard. Responders are defined as patients with < 10% viable residual tumor cells (Mandard-score).Difference in accuracy (area under ROC curve) and negative predictive value between FDG-PET and CT-scan are primary endpoints. Furthermore, an economic evaluation will be performed, comparing survival and costs associated with the use of FDG-PET (or CT-scan) to predict tumor response with survival and

Details

Database :
OAIster
Journal :
BMC Medical Physics; 3; 3; 1756-6649; 31-07-2008; vol. 8; ~BMC Medical Physics~3~3~~~1756-6649~31-07-2008~8~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1298877791
Document Type :
Electronic Resource