6683 ABVD is the standard treatment of advanced Hodgkin’s disease(HD). However two of the components,Bleomycin and DTIC have significant toxcicities such as lung fibrosis and emesis,and also uncertain single agent activity. The EVA regimen (VP16,Vinblastine and Doxurubicin) is an attempt to substitute a known active agent ie:VP16 for Bleo and DTIC. A series of 26 pts with advanced HD and a history of prior lung disease or radiation treatment were selected for this study. They included 7 stage2/bulky mediastinal tumors and all received consolidation XRT. The remaining pts recieved EVA only. The median F/U was 108n months. EVA: Etoposide 100mg/m2 days 1–3,VBL 6mg/m2 day-1 and Doxurubicin 50mg/m2 day-1. All drugs given iv. Cycles repeated Q.3 wk x 6 cycles. Results: Complete response(CR) was achieved in 25/26(96%). Of these 25 responders 8 pts relapsed in a median of 10 months(range 3–22). In F/U 17/26 pts had no evidence of recurrent HD, resulting in progression-free survival for the entire group of 65% at 108 mo. Five of the 8 relapsers achieved a 2nd-CR and were alive and disease-free at F/U at 108 mo. In the entire series 4 pts(15%) died of HD (one patient was induction failure and 3 pts relapsed post 1st CR). 22/26(85%) of pts continued free of disease. There was no pulmonary toxicity. Toxicities in general was comparable to ABVD. Conclusion: The EVA regimen has an overall survival comparable to standard ABVD in our study with the added advantage of lacking lung toxicity in this susceptible group of pts. No significant financial relationships to disclose.