B LEOMYCIN (BLM) is a glycoprotein antibiotic synthesized from Streptomyces verticillus that is highly effective against malignancies such as lymphomas, dysgenetic testicular tumors, and squamous cell carcinomas. It is often used in conjunction with other agents because of its low potential for bone marrow suppression or immunosuppression, thereby enhancing the antineoplastic effect at the cost of fewer side effects.’ Pulmonary toxicity that presents as an interstitial pneumonitis that may progress to fibrosis is its major side effect.* Patients more than 65 years of age and those with persisting pulmonary pathology are especially at risk. Pulmonary fibrosis occurs in 3% of patients receiving BLM. A hypersensitivity pneumonitis and fulminant respiratory failure can also occur.3 Asymptomatic changes in pulmonary function that may be construed as milder forms of toxicity are probably more common.4,5 Radiation to the chest and oxygen therapy are believed to potentiate BLM pulmonary toxicity. A high or even modestly elevated F,02 (0.33) has been thought to be responsible for postoperative respiratory failure and subsequent deaths.‘.6 In addition, exacerbations of recognized or occult pulmonary fibrosis may occur with other antineoplastic agents (eg, busulfan, methotrexate, cyclophosphamide) following 0, therapy.‘.’ The anesthesiologist may be required to manage a case for the removal of retroperitoneal lymph nodes or pulmonary metastasis following BLM chemotherapy. Even if the lymph nodes show no metastatic disease, they are large, fibrotic, sclerotic, and often attached to neighboring structures. This makes surgery technically difficult, prolonged, accompanied by considerable blood loss, and may involve the resection of the large bowel, aorta, inferior vena cava, or a kidney.6 Resection of pulmonary metastases has the potential problem of the need for one-lung anesthesia during thoracotomy, and the consequent risk of the use of an increased F,O, to avoid hypoxia. A patient who may have been at risk for reactivation of BLM lung toxicity when he underwent myocardial revascularization during hypothermic cardiopulmonary bypass (CPB) is reported. The use of an Oximetric pulmonary artery catheter (PAC) in combination with peripheral pulse oximetry ensured adequate oxygenation while the patient received restricted 0, therapy during and after surgery.