Your browser doesn't support javascript.
loading
Identifying the location of locoregional recurrences after definitive radiotherapy for head and neck cancer using metabolic parameters of baseline and mid-treatment 18F-FDG-PET scans.
Aren, Ewa; Trada, Yuvnik; Lee, Mark; Deshpande, Shrikant; Jameson, Michael G; Johnston, Meredith; Berry, Megan; Estall, Vanessa; Fowler, Allan.
Affiliation
  • Aren E; Cancer Therapy Centre, Liverpool Hospital, Sydney, New South Wales, Australia.
  • Trada Y; Calvary Mater Newcastle, Newcastle, New South Wales, Australia.
  • Lee M; Faculty of Medicine, The University of Sydney, Sydney, New South Wales, Australia.
  • Deshpande S; Cancer Therapy Centre, Liverpool Hospital, Sydney, New South Wales, Australia.
  • Jameson MG; Cancer Therapy Centre, Liverpool Hospital, Sydney, New South Wales, Australia.
  • Johnston M; Faculty of Medicine, The University of New South Wales, Sydney, New South Wales, Australia.
  • Berry M; Faculty of Medicine, The University of New South Wales, Sydney, New South Wales, Australia.
  • Estall V; GenesisCare, Sydney, New South Wales, Australia.
  • Fowler A; Cancer Therapy Centre, Liverpool Hospital, Sydney, New South Wales, Australia.
J Med Imaging Radiat Oncol ; 67(1): 89-97, 2023 Feb.
Article in En | MEDLINE | ID: mdl-36300564
ABSTRACT

INTRODUCTION:

Tumour recurrences after treatment of head and neck squamous cell carcinoma (HNSCC) are more likely to originate from regions of high-baseline FDG-PET uptake. Mid-treatment functional imaging can potentially predict for higher risk of tumour recurrence. The aim of this study is to correlate the location of locoregional tumour recurrence with baseline FDG-PET metabolic volumes and mid-treatment FDG-PET metabolic volumes in patients with HNSCC following definitive radiotherapy.

METHODS:

A total of 23 patients with 26 local and/or regional recurrences underwent baseline (W0-PET) and mid-treatment (W3-PET) 18F-FDG PET scans as part of their radiotherapy. FDG-PET-based metabolic volumes (MTV20%, MTV40%, MTV60%, MTV80%, SUV2.5, SUVpeak and PET_EDGE) were delineated onto the FDG-PET scans. The recurrence nidus was identified on FDG-PET at the time of recurrence (REC-PET). DIR-based fusion was performed for REC-PET to W0-PET, and REC-PET to W3-PET. The location of the recurrence nidus was correlated with the FDG-PET volumes. Further analysis included a comparison of the recurrence density to FDG-PET metabolic volumes.

RESULTS:

Most recurrences occurred within the MTV20%, MTV40% and SUV 2.5 volumes. Sixty-nine per cent of recurrences (18 of 26) occurred within both the W0 MTV40% and W3 MTV40% volumes. A higher recurrence density was seen for iso-SUV contours closer to the maximum SUV for both W0 and W3. For a number of the FDG-PET volumes, including MTV20%, MTV40% and SUV2.5, the recurrence density was improved for W3 compared to W0, however, this improvement was small in magnitude. The average volume of MTV40% contours was considerably smaller than MTV20% and SUV2.5 contours.

CONCLUSION:

The metabolic parameters of SUV2.5, MTV20% and MTV40% delineated on the baseline and mid-treatment FDG-PET scans encompassed the majority of recurrences. The MTV40% is significantly smaller, hence, we prefer this volume for future dose escalation studies.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Fluorodeoxyglucose F18 / Head and Neck Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Fluorodeoxyglucose F18 / Head and Neck Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Year: 2023 Type: Article