The management of patients with Hodgkin's Disease (HD) has been one of the major successes of clinical oncology in this century. Three of every four patients can be expected to be cured of this previously uniformly fatal disease [1,2]. Most patients with advanced disease achieve durable remissions and long-term survival when treated with combination chemotherapy. Patients who fail to attain a complete remission after treatment with one of the standard chemotherapy regimens have the poorest prognosis. Although they sometimes respond to a non-cross-resistant program, these remissions usually are brief. New drugs are needed to be tested in refractory patients to one or more salvage regimens and for those who are not candidate for high-dose chemotherapy with bone marrow or peripheral stem transplantation. We report a case of a patient with primary refractory HD who failed one standard and two salvage chemotherapy regimens and achieved a complete remission following treatment with paclitaxel (Taxol). A 34-year-old white man presented in March 1994 with dyspnea, bloody sputum, night sweats, and weight loss. He was found to have a 10 × 7-cm mediastinal mass on computed tomography (CT) of the chest. Mediastinoscopy and video assisted thoracoscopy revealed a large tumor, which on pathologic study was consistent with nodular sclerosing HD. Following appropriate staging, he was found to have bulky stage IIB disease with mediastinal and cervical lymphadenopathy. He received the standard MOPP/ABV hybrid regimen and achieved a partial response radiographically; however, by completion of the sixth cycle his mediastinal mass demonstrated some regrowth and he was referred for radiation therapy. He received a total of 4,050 Cgy to the mediastinum and completed treatment in December 1994. His mediastinal mass failed to demonstrate any reduction in size. A gallium scan showed focal uptake within the mediastinal mass consisting with residual disease. In February 1995 he was referred to a bone marrow transplant center. It was felt that he was not a candidate for high-dose chemotherapy because of obstructive and restrictive lung disease. He then received two courses of etoposide, cisplatin, cytarabine, and methylprednisolone along with G-CSF because of postchemotherapy neutropenia. His tumor failed to respond in size and he refused any further treatment at that time. Serial chest X-rays demonstrated disease stability until late June 1996 when his mediastinal mass showed significant regrowth with the appearance of new left lung nodules. He then received two cycles of prednisone, etoposide, chlorambucil, and CCNU with 25% reduction in the mediastinal mass and 50% reduction in the lung nodules. Two additional cycles failed to produce any further response and treatment was discontinued. Within a few months later, his B symptoms recurred and by December 1997 he was found to have bilateral multiple pulmonary nodules of 1 to 2 cm each. An open lung biopsy demonstrated recurrent HD. One month later his pulmonary nodules progressed. He then re...