IONIZING irradiation has an important role today in cancer therapy, both as an adjunct to surgery and as a primary treatment. Methods of increasing the effectiveness of irradiation have been sought, and numerous studies have been carried out in an attempt to elucidate the factors which alter the radiosensitivity of tumor cells (1). The amount of oxygen available to tissues at the time of irradiation is recognized as an important factor in their radiosensitivity. The radiosensitizing effect of oxygen on normal tissue is well documented (3-5) (Fig. 1). The premise that anemia decreases tissue radiosensitivity has long been accepted by radiotherapists, and correction of the anemia has been recommended as a means of increasing the effectiveness of irradiation (7). This concept is based upon an assumed correlation between anemia and reduced tissue oxygen tension. The present study was undertaken to assess the effect of anemia on the radiosensitivity of animal tumor tissue. Material and Methods New Zealand white rabbits weighing between 2 and 5 kg and bearing Rous V2 sarcoma in the thigh muscle were used as our biological system. Tumor tissue from the periphery of carrier rabbit V2 sarcoma was minced, homogenized, and filtered through a 56-mesh stainless-steel screen to remove clumped cells. The filtered cells were suspended in normal saline, counted on a standard white blood cell counting slide, and injected into the subcutaneous tissue of the thigh of male New Zealand white rabbits. In all cases, approximately 2.0 X 106 cells in 2 cc of total suspension were injected. Tumors measuring 1–4 cm in diameter were palpable and visible seventeen to twenty days after injection of the cells. At this time the animals were randomly divided into anemic and control groups. For the purpose of this experiment anemia is defined as 9 to 10 g of hemoglobin per 100 ml of blood. Preliminary studies on rabbits showed a consistent relation between body weight and blood volume as measured by radioactive iodinated serum albumin technic. To induce anemia the rabbit was anesthetized with intravenous Nembutal, and a laparotomy was performed. A beveled polyethylene cannula (P.E. 60) was inserted into the inferior vena cava and 30 to 35 per cent of the rabbit's calculated blood volume was withdrawn into a heparinized syringe over a period of fifteen to thirty minutes. The withdrawn blood was centrifuged, and serum was reinjected into the vena cava to obtain a near normal volume in the intravascular compartment. The extra volume of serum was obtained from donor rabbits which were not part of the experimental group. The cannula was sutured in place, the abdomen closed with the end of the cannula protruding, and thirty minutes later the animal was irradiated. This thirty-minute delay was allowed for hemodynamic equilibration.
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