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
. 2014 Mar 5:8:405.
doi: 10.3332/ecancer.2014.409. eCollection 2014.

The role of [(18)F]FDG-PET/CT in staging and treatment planning for volumetric modulated Rapidarc radiotherapy in cervical cancer: experience of the European Institute of Oncology, Milan, Italy

Affiliations

The role of [(18)F]FDG-PET/CT in staging and treatment planning for volumetric modulated Rapidarc radiotherapy in cervical cancer: experience of the European Institute of Oncology, Milan, Italy

Roberta Lazzari et al. Ecancermedicalscience. .

Abstract

Rationale: to evaluate the role of 18F-fluorodeoxyglucose positron emission tomography ([(18)F]FDG-PET) integrated with computer tomography (CT) scan [(18)F]FDG-PET/CT in the staging and target volume definition in Intensity Modulated RapidarcTM Delivery (RA-IMRT) in cervical cancer.

Methods: From June 2010 to December 2011, 66 patients affected by cervical cancer, candidates for definitive or adjuvant radiochemotherapy, underwent standard staging with CT and magnetic resonance imaging (MRI). All patients underwent [(18)F]FDG-PET/CT in order to exclude distant metastases and to define gross tumor volume (GTV). 40 and 26 patients received exclusive and adjuvant radiotherapy, respectively. RA-IMRT with simultaneous integrated boost (SIB) to the positive disease technique was employed.

Results: [(18)F]FDG-PET/CT has changed the stage, and radiotherapy treatment planning was modified in 25% and 7.7 % of patients that received definitive and adjuvant radiotherapy, respectively. Particularly [(18)F]FDG-PET/CT imaging showed metabolically active tumor in lymph nodes area, therefore the stage and the treatment planning changed for these patients.

Conclusions: [(18)F]FDG-PET/CT leads to a better staging and definition of disease and has the potential of showing lymph-node metastasis not only within the pelvis but also in the para-aortic area. In addition, [(18)F]FDG-PET/CT is useful for better definition of the target volume and to produce a 'dose painted' treatment. This might also open the field for escalation dose regimens.

Keywords: ([18F]FDG-PET/CT); IMRT; Rapidarc radiotherapy; cervical cancer.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.. Axial T2 and T1 images showing a partially necrotic left external iliac node (arrow).
Figure 2.
Figure 2.. [18F]FDG-PET/CT has a higher sensitivity than CT in depicting lymph node metastatic.

References

    1. Kidd EA, et al. Changes in cervical cancer FDG uptake during chemoradiation and association with response. Int J Radiat Oncol Biol Phys. 2013;85:116–22. doi: 10.1016/j.ijrobp.2012.02.056. - DOI - PMC - PubMed
    1. Schwarz JK, et al. 18F-fluorodeoxyglucose positron emission tomography evaluation of early metabolic response during radiation therapy for cervical cancer. Int J Radiat Oncol Biol Phys. 2008;72:1502–7. doi: 10.1016/j.ijrobp.2008.03.040. - DOI - PubMed
    1. Kidd EA, et al. Lymph node staging by positron emission tomography in cervical cancer: relationship to prognosis. J Clin Oncol. 2010;85:2108–13. doi: 10.1200/JCO.2009.25.4151. - DOI - PubMed
    1. Yildirim Y, et al. Integrated PET/CT for the evaluation of para-aortic nodal metastasis in locally advanced cervical cancer patients with negative conventional CT findings. Gynecol Oncol. 2008;108:154–9. doi: 10.1016/j.ygyno.2007.09.011. - DOI - PubMed
    1. Esthappan J, et al. Treatment planning guidelines regarding the use of CT/PET guided IMRT for cervical carcinoma with positive para-aortic lymph-nodes. Int J Radiat Oncol Biol Phys. 2004;58:1289–97. doi: 10.1016/j.ijrobp.2003.09.074. - DOI - PubMed

LinkOut - more resources