Journal article
Is there a role for an FDG derived biological boost in squamous cell anal cancer?
- Abstract:
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Aim We aim to investigate the potential role for a biological boost in anal cancer by assessing whether subvolumes of high FDG avidity, identified at outset, are spatially consistent during a course of chemoradiotherapy (CRT).
Methods FDG-PET scans from 21 patients enrolled into the ART study (NCT02145416) were retrospectively analysed. A total of twenty-nine volumes including both primary tumours and involved nodes >2 cm were identified. FDG-PET scans were performed prior to treatment and day 8 or 9 of CRT. FDG subvolumes were created using a percentage of maximum FDG avidity at thresholds of 34%, 40%, 50%, on the pre-treatment scans, and 70% and 80% on the subsequent scans. Both FDG-PET scans were deformably registered to the planning CT scan. The overlap fraction (OF) and vector distance (VD) were calculated to assess spatial consistency. FDG subvolumes for further investigation had OF >0.7, as this has been defined in previous publications as a “good” correlation.
Results The median OF between the diagnostic FDG-PET subvolumes 34%, 40% and 50% of max SUV and subsequent FDG-PET subvolumes of 70% of max SUV were 0.97, 0.92 and 0.81. The median OF between the diagnostic FDG-PET subvolumes 34%, 40% and 50% and subsequent FDG-PET subvolumes of 80% were 1.00, 1.00 and 0.92. The median (range) VD values between diagnostic FDG-PET subvolumes 34%, 40% and 50% and subsequent FDG-PET subvolumes of 80% were 0.74mm (0.19-2.94) 0.74mm (0.19-3.39) and 0.71 (0.2-3.29) respectively. Twenty out of 29 volumes (69.0%) achieved a threshold of >0.7 between the FDG 50% subvolume on the diagnostic scan and the FDG 80% subvolume on the subsequent scan.
Conclusion FDG avid subvolumes identified at baseline were spatially consistent during a course of CRT treatment. The subvolume of 50% of SUVmax on the pre-treatment scan could be considered as a potential target for dose escalation.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Accepted manuscript, pdf, 3.4MB, Terms of use)
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- Publisher copy:
- 10.1016/j.clon.2018.11.034
Authors
+ Medical Research Council
More from this funder
- Funding agency for:
- Hawkins, M
- Grant:
- MC_UU_00001/2
- Publisher:
- Elsevier
- Journal:
- Clinical Oncology More from this journal
- Volume:
- 31
- Issue:
- 2
- Pages:
- 72-80
- Publication date:
- 2018-12-21
- Acceptance date:
- 2018-11-08
- DOI:
- ISSN:
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0938-7714
- Keywords:
- Pubs id:
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pubs:943643
- UUID:
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uuid:976028f9-9e47-4115-b615-dc098fac4e1b
- Local pid:
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pubs:943643
- Source identifiers:
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943643
- Deposit date:
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2018-11-27
- ARK identifier:
Terms of use
- Copyright holder:
- Elsevier Ltd
- Copyright date:
- 2018
- Notes:
- © 2018 Published by Elsevier Ltd on behalf of The Royal College of Radiologists. This is the accepted manuscript version of the article. The final version is available online from Elsevier at: https://doi.org/10.1016/j.clon.2018.11.034
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