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Sökning: id:"swepub:oai:DiVA.org:uu-237885" > In Vivo Quantificat...

In Vivo Quantification of Hypoxic and Metabolic Status of NSCLC Tumors Using [18F]HX4 and [18F]FDG-PET/CT Imaging.

Zegers, Catharina M L (författare)
Maastricht University Medical Centre
van Elmpt, Wouter (författare)
Maastricht University Medical Centre
Reymen, Bart (författare)
Maastricht University Medical Centre
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Even, Aniek J G (författare)
Maastricht University Medical Centre
Troost, Esther G C (författare)
Maastricht University Medical Centre
Ollers, Michel C (författare)
Maastricht University Medical Centre
Hoebers, Frank J P (författare)
Maastricht University Medical Centre
Houben, Ruud M A (författare)
Maastricht University Medical Centre
Eriksson, Jonas (författare)
VU University Medical Centre, Amsterdam
Windhorst, Albert D (författare)
VU University Medical Centre, Amsterdam
Mottaghy, Felix M (författare)
Maastricht University Medical Centre
De Ruysscher, Dirk (författare)
Maastricht University Medical Centre
Lambin, Philippe (författare)
Maastricht University Medical Centre
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 (creator_code:org_t)
2014
2014
Engelska.
Ingår i: Clinical cancer research. - 1078-0432. ; 20:24, s. 6389-6397
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • PURPOSE: Increased tumor metabolism and hypoxia are related to poor prognosis in solid tumors, including non-small cell lung cancer (NSCLC). PET imaging is a noninvasive technique that is frequently used to visualize and quantify tumor metabolism and hypoxia. The aim of this study was to perform an extensive comparison of tumor metabolism using 2[(18)F]fluoro-2-deoxy-d-glucose (FDG)-PET and hypoxia using HX4-PET imaging.EXPERIMENTAL DESIGN: FDG- and HX4-PET/CT images of 25 patients with NSCLC were coregistered. At a global tumor level, HX4 and FDG parameters were extracted from the gross tumor volume (GTV). The HX4 high-fraction (HX4-HF) and HX4 high-volume (HX4-HV) were defined using a tumor-to-blood ratio > 1.4. For FDG high-fraction (FDG-HF) and FDG high-volume (FDG-HV), a standardized uptake value (SUV) > 50% of SUVmax was used. We evaluated the spatial correlation between HX4 and FDG uptake within the tumor, to quantify the (mis)match between volumes with a high FDG and high HX4 uptake.RESULTS: At a tumor level, significant correlations were observed between FDG and HX4 parameters. For the primary GTV, the HX4-HF was three times smaller compared with the FDG-HF. In 53% of the primary lesions, less than 1 cm(3) of the HX4-HV was outside the FDG-HV; for 37%, this volume was 1.9 to 12 cm(3). Remarkably, a distinct uptake pattern was observed in 11%, with large hypoxic volumes localized outside the FDG-HV.CONCLUSION: Hypoxic tumor volumes are smaller than metabolic active volumes. Approximately half of the lesions showed a good spatial correlation between the PET tracers. In the other cases, a (partial) mismatch was observed. The addition of HX4-PET imaging has the potential to individualize patient treatment. Clin Cancer Res; 1-9. ©2014 AACR.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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