Literature DB >> 21331930

FDG PET and PET/CT for colorectal cancer.

Dominique Delbeke1, William H Martin.   

Abstract

The evaluation of patients with known or suspected recurrent colorectal carcinoma is now an accepted indication for positron emission tomography using (18)F-fluorodeoxyglucose (FDG-PET) imaging. PET and CT are complimentary, and therefore, integrated PET/CT imaging should be performed where available. FDG-PET/CT is indicated as the initial test for diagnosis and staging of recurrence, and for preoperative staging (N and M) of known recurrence that is considered to be resectable. FDG-PET imaging is valuable for the differentiation of posttreatment changes from recurrent tumor, differentiation of benign from malignant lesions (indeterminate lymph nodes, hepatic, and pulmonary lesions), and the evaluation of patients with rising tumor markers in the absence of a known source. The addition of FDG-PET/CT to the evaluation of these patients reduces overall treatment costs by accurately identifying patients who will and will not benefit from surgical procedures. This new powerful technology provides more accurate interpretation of both CT and FDG-PET images and therefore more optimal patient care. PET/CT fusion images affect the clinical management by guiding further procedures (biopsy, surgery, and radiation therapy), excluding the need for additional procedures, and changing both inter- and intramodality therapy.

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Year:  2011        PMID: 21331930     DOI: 10.1007/978-1-61779-062-1_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  4 in total

1.  Imaging spectrum of peritoneal carcinomatosis on FDG PET/CT.

Authors:  Ameya D Puranik; Nilendu C Purandare; Archi Agrawal; Sneha Shah; Venkatesh Rangarajan
Journal:  Jpn J Radiol       Date:  2014-08-14       Impact factor: 2.374

2.  PET scans as a predictive marker of survival in advanced colorectal cancer.

Authors:  Minsig Choi; Sri Lakshmi S Kollepara; Lance K Heilbrun; Daryn Smith; Anthony F Shields; Philip A Philip
Journal:  Clin Colorectal Cancer       Date:  2014-10-23       Impact factor: 4.481

3.  Modulated electro-hyperthermia induced p53 driven apoptosis and cell cycle arrest additively support doxorubicin chemotherapy of colorectal cancer in vitro.

Authors:  Tamas Vancsik; Gertrud Forika; Andrea Balogh; Eva Kiss; Tibor Krenacs
Journal:  Cancer Med       Date:  2019-06-10       Impact factor: 4.452

4.  Butyrate decreases its own oxidation in colorectal cancer cells through inhibition of histone deacetylases.

Authors:  Anna Han; Natalie Bennett; Bettaieb Ahmed; Jay Whelan; Dallas R Donohoe
Journal:  Oncotarget       Date:  2018-06-05
  4 in total

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