Microregional fluctuations in perfusion within human tumours detected using laser Doppler flowmetry.

PURPOSE Transient fluctations in erythrocyte flux consistent with perfusion driven hypoxia have been previously reported using experimental tumour models. The present study was designed to establish whether such changes are a common feature of human tumours. METHODS AND MATERIALS A multi-channel laser Doppler system was used to monitor microregional changes in flow in human tumours. Eight individual tumours were investigated, two primary and one locally recurrent breast carcinoma, two metastatic skin deposits and three metastatic lymph nodes. Six custom designed microprobes (diameter of 300 microns), each monitoring a nominal sampling volume of approximately 10(-2) mm3 were inserted into the tumour and perfusion monitored over a period of 60 min. RESULTS The results show that in 54% of the regions monitored there was a change in microregional blood flow by a factor of 1.5 or more. Over the whole 60-min period, 19% of the changes were reversed, with a time course of 4-44 min. CONCLUSIONS This finding demonstrates that microregional fluctuations in perfusion occur frequently in human tumours. Furthermore, the observation that 19% of the changes were reversed implies that at least some of the cells are subject to transient acute hypoxia.

[1]  M Intaglietta,et al.  Biological zero of laser Doppler fluxmetry: microcirculatory correlates in the hamster cheek pouch during flow and no flow conditions. , 1993, International journal of microcirculation, clinical and experimental.

[2]  G. Nilsson,et al.  Influence of fibre diameter and probe geometry on the measuring depth of laser Doppler flowmetry in the gastrointestinal application. , 1991, International journal of microcirculation, clinical and experimental.

[3]  L. H. Gray,et al.  The Histological Structure of Some Human Lung Cancers and the Possible Implications for Radiotherapy , 1955, British Journal of Cancer.

[4]  R. Gatenby,et al.  Oxygen distribution in squamous cell carcinoma metastases and its relationship to outcome of radiation therapy. , 1988, International journal of radiation oncology, biology, physics.

[5]  D. Chaplin,et al.  Intermittent blood flow in a murine tumor: radiobiological effects. , 1987, Cancer research.

[6]  S. Hill,et al.  Temporal heterogeneity in microregional erythrocyte flux in experimental solid tumours. , 1995, British Journal of Cancer.

[7]  Abbot Nc,et al.  Biological zero in laser Doppler measurements in normal, ischaemic and inflamed human skin. , 1993 .

[8]  M. Trotter,et al.  Effect of nicotinamide on the microregional heterogeneity of oxygen delivery within a murine tumor. , 1990, Journal of the National Cancer Institute.

[9]  P Vaupel,et al.  Intratumoral pO2 predicts survival in advanced cancer of the uterine cervix. , 1993, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[10]  J. Brown,et al.  Mechanism of action of the selective tumor radiosensitizer nicotinamide. , 1988, International journal of radiation oncology, biology, physics.

[11]  M. Trotter,et al.  The use of fluorescent probes to identify regions of transient perfusion in murine tumors. , 1989, International journal of radiation oncology, biology, physics.

[12]  M. Lemmon,et al.  Mechanism of action and clinical potential of the selective tumor radiosensitizer nicotinamide , 1987 .

[13]  J M Brown,et al.  Evidence for acutely hypoxic cells in mouse tumours, and a possible mechanism of reoxygenation. , 1979, The British journal of radiology.