Tumoural perfusion as measured by dynamic computed tomography in head and neck carcinoma.

PURPOSE To investigate the intra- and interobserver variability, as well as the intra- and interpatient variability of CT-determined tumour perfusion in head and neck tumours, and to evaluate the preliminary value of this parameter as predictive factor of local failure after treatment by definitive radiotherapy. MATERIALS AND METHODS In 41 patients the perfusion of a primary head and neck squamous cell carcinoma was estimated using dynamic CT. A 40-ml intravenous bolus of a low-osmolar non-ionic contrast agent was rapidly injected over 5 s (8 ml/s), while a dynamic acquisition of image data was obtained during the first pass at the level of the largest axial tumour surface. A time-density curve was constructed for the primary tumour and the carotid artery. The perfusion in the selected tumour region of interest was calculated by dividing the slope of the tumour-time density curve by the maximal value in arterial density. Tumour volume was calculated on the CT-images and correlated with perfusion rate. RESULTS The mean perfusion rate was 86.4 ml/min per 100 g (median, 80.6; SD, 43.05; range, 31.7-239.8 ml/min per 100 g). No systematic difference was found between the measurements performed by two independent observers. The intratumoural COV was 0.22, the intertumoural COV 0.37. No correlation was found with tumour volume. Ten out of 20 patients with a perfusion rate < 80 ml/min per 100 g were not locally controlled, while nine out of 21 patients with a value > 80 ml/min per 100 g did show a local failure (P = 0.19). CONCLUSIONS CT-determined perfusion measurements of head and neck tumours are feasible. No correlation with tumour volume and a sufficiently large COV were found to consider this parameter as a possible prognostic factor for outcome after radiotherapy. More patients need to be investigated to test the hypothesis that tumours with a low CT determined perfusion rate have a higher risk of local failure.

[1]  A L Baert,et al.  Non-invasive tumour perfusion measurement by dynamic CT: preliminary results. , 1997, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[2]  M. Dewhirst,et al.  Tumor oxygenation predicts for the likelihood of distant metastases in human soft tissue sarcoma. , 1996, Cancer research.

[3]  H. Awwad,et al.  Intercapillary distance measurement as an indicator of hypoxia in carcinoma of the cervix uteri. , 1986, International journal of radiation oncology, biology, physics.

[4]  M. Bahner,et al.  Regional blood flow, capillary permeability, and compartmental volumes: measurement with dynamic CT--initial experience. , 1999, Radiology.

[5]  Beverly A. Teicher,et al.  Drug resistance in oncology , 1993 .

[6]  J. Overgaard,et al.  Modification of Hypoxia-Induced Radioresistance in Tumors by the Use of Oxygen and Sensitizers. , 1996, Seminars in radiation oncology.

[7]  J. Overgaard,et al.  Pretreatment oxygenation predicts radiation response in advanced squamous cell carcinoma of the head and neck. , 1996, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[8]  À. Rovira,et al.  31Phosphorus magnetic resonance spectroscopy in the assessment of head and neck tumors. , 1998, International journal of radiation oncology, biology, physics.

[9]  L. Révész,et al.  Variation of vascular density within and between tumors of the uterine cervix and its predictive value for radiotherapy. , 1989, International journal of radiation oncology, biology, physics.

[10]  J. W. Beck,et al.  Volume determinations using computed tomography. , 1982, AJR. American journal of roentgenology.

[11]  J C Ehrhardt,et al.  Tumor perfusion studies using fast magnetic resonance imaging technique in advanced cervical cancer: a new noninvasive predictive assay. , 1996, International journal of radiation oncology, biology, physics.

[12]  P Vaupel,et al.  Association between tumor hypoxia and malignant progression in advanced cancer of the uterine cervix. , 1996, Cancer research.

[13]  P. Okunieff,et al.  Blood flow, oxygen and nutrient supply, and metabolic microenvironment of human tumors: a review. , 1989, Cancer research.

[14]  L D Buadu,et al.  Breast lesions: correlation of contrast medium enhancement patterns on MR images with histopathologic findings and tumor angiogenesis. , 1996, Radiology.

[15]  F. Howe,et al.  The response to carbogen breathing in experimental tumour models monitored by gradient-recalled echo magnetic resonance imaging. , 1997, British Journal of Cancer.

[16]  H. Lyng,et al.  Oxygen tension and vascular density in human cervix carcinoma. , 1996, British Journal of Cancer.

[17]  P Kolstad,et al.  Intercapillary distance, oxygen tension and local recurrence in cervix cancer. , 1968, Scandinavian journal of clinical and laboratory investigation. Supplementum.

[18]  A. W. Simonetti,et al.  Characterization and validation of noninvasive oxygen tension measurements in human glioma xenografts by 19F-MR relaxometry. , 1999, International journal of radiation oncology, biology, physics.