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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 

Tumor hypoxia imaging with [f-18] fluoromisonidazole positron emission tomography in head and neck cancer.

PURPOSE: Advanced head and neck cancer shows hypoxia that results in biological changes to make the tumor cells more aggressive and less responsive to treatment resulting in poor survival. [F-18] fluoromisonidazole (FMISO) positron emission tomography (PET) has the ability to noninvasively quantify regional hypoxia. We investigated the prognostic effect of pretherapy FMISO-PET on survival in head and neck cancer. EXPERIMENTAL DESIGN: Seventy-three patients with head and neck cancer had pretherapy FMISO-PET and 53 also had fluorodeoxyglucose (FDG) PET under a research protocol from April 1994 to April 2004. RESULTS: Significant hypoxia was identified in 58 patients (79%). The mean FMISO tumor/blood(max) (T/B(max)) was 1.6 and the mean hypoxic volume (HV) was 40.2 mL. There were 28 deaths in the follow-up period. Mean FDG standard uptake value (SUV)(max) was 10. 8. The median time for follow-up was 72 weeks. In a univariate analysis, T/B(max) (P = 0.002), HV (P = 0.04), and the presence of nodes (P = 0.01) were strong independent predictors. In a multivariate analysis, including FDG SUV(max), no variable was predictive at P < 0.05. When FDG SUV(max) was removed from the model (resulting in n = 73 with 28 events), nodal status and T/B(max) (or HV) were both highly predictive (P = 0.02, 0.006 for node and T/B(max), respectively; P = 0.02 and 0.001 for node and HV, respectively). CONCLUSIONS: Pretherapy FMISO uptake shows a strong trend to be an independent prognostic measure in head and neck cancer.[1]

References

  1. Tumor hypoxia imaging with [f-18] fluoromisonidazole positron emission tomography in head and neck cancer. Rajendran, J.G., Schwartz, D.L., O'sullivan, J., Peterson, L.M., Ng, P., Scharnhorst, J., Grierson, J.R., Krohn, K.A. Clin. Cancer Res. (2006) [Pubmed]
 
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