Abstract
A new treatment program was developed in an attempt to increase the complete remission rate and survival of previously untreated patients with advanced stages of diffuse aggressive lymphomas. A flexible number of cycles of ProMACE chemotherapy (prednisone, methotrexate, doxorubicin, cyclophosphamide, and epipodophyllotoxin VP-16) was alternated with a flexible number of cycles of MOPP chemotherapy (mechlorethamine, vincristine sulfate, procarbazine, and prednisone), and finally late intensification with ProMACE therapy was given. The duration of each phase of treatment was determined by the patient''s rate of tumor response. Complete remissions were achieved in 55 of 74 patients (74%) with a median duration of follow-up exceeding 2.5 yr. Only 10 of the complete responders (18%) have had relapse. The dose-limiting toxicity is myelosuppression, and 8 patients (10%) died from sepsis. Median survival for all patients has not been reached but is predicted to exceed 4 yr with 65% of patients alive at 4 yr. Previously a 46% complete remission rate was achieved with 38% of all patients alive at 4 yr; relapse-free survival beyond 2 yr was tantamount to cure. Therefore, ProMACE-MOPP chemotherapy represents a substantial improvement in treating patients with diffuse aggressive lymphomas.