Respiratory-gated (4D) FDG-PET detects tumour and normal lung response after stereotactic radiotherapy for pulmonary metastases

Authors

  • Shankar Siva Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia; Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
  • Jason W. Callahan Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
  • Tomas Kron Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia; Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
  • Brent Chesson Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
  • Stephen A. Barnett Division of Cancer Surgery, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
  • Michael P. Macmanus Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia; Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
  • Rodney J. Hicks Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia; Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia
  • David L. Ball Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia; Division of Radiation Oncology and Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia

DOI:

https://doi.org/10.3109/0284186X.2015.1027409

Abstract

Background. Response assessment after stereotactic ablative body radiotherapy (SABR) in lung can be confounded by radiation-induced inflammation, fibrosis and subsequent alteration of tumour motion. The purpose of this prospective pilot study was to evaluate the utility of four-dimensional (4D) FDG-PET/CT for post-SABR tumour and normal lung response assessment in pulmonary oligometastases.

Material and methods. Patients enrolled from February 2010 to December 2011 in this prospective ethics approved study had 1–2 pulmonary metastases on staging FDG-PET. Serial contemporaneous 3D and 4D FDG-PET/CT scans were performed at baseline, 14 days and 70 days after a single fraction of 26 Gy SABR. Tumour response was evaluated in 3D and 4D using SUVmax, RECIST and PERCIST criteria. Normal lung radiotoxicity was evaluated using SUVmean within 0–2 Gy, 2–5 Gy, 5–10 Gy, 10–20 Gy and 20 + Gy isodose volumes.

Results. In total, 17 patients were enrolled of which seven were ineligible due to interval progression from staging PET to baseline 4D-PET. The mean time between scans was 62 days. At a median follow-up of 16 months, 10 patients with 13 metastases received SABR, with no patient having local progression. The vector of tumour motion was larger in patients with discordant 3D and 4D PET PERCIST response (p < 0.01), with a mean (± SEM) motion of 10.5 mm (± 0.96 mm) versus 6.14 mm (± 0.81 mm) in those patients with concordant 3D and 4D response. Surrounding normal lung FDG uptake at 70 days was strongly correlated to delivered radiation dose (r2 = 0.99, p < 0.01), with significant elevations across all dose levels (p ≤ 0.05), except the < 2 Gy volume (p = 0.30).

Conclusions. We demonstrate high rates of interval progression between staging PET scans in patients with oligometastases. We found that tumour response on conventional 3D PET is not concordant with 4D PET for tumours with large motion. Normal lung metabolic uptake is strongly dose dependent after SABR, a novel finding that should be further validated.

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Published

2015-09-14

How to Cite

Siva, S., Callahan, J. W., Kron, T., Chesson, B., Barnett, S. A., Macmanus, M. P., … Ball, D. L. (2015). Respiratory-gated (4D) FDG-PET detects tumour and normal lung response after stereotactic radiotherapy for pulmonary metastases. Acta Oncologica, 54(8), 1105–1112. https://doi.org/10.3109/0284186X.2015.1027409