Summary:OS yet to reach a median at 8 years and a PFS of 44 months, significantly better than non IFN high-dose A single centre series of 195 consecutive newly diagpatients (P Ͻ 0.0036). However, although we showed nosed untreated myeloma patients under 70 years, seen benefit for selected patients in studies and trials between September 1986 and March 1994, were ana-(particularly with IFN) during the 8-year period of the lysed to assess the impact of current intensive treatment series, this did not translate into overall PFS benefit in methods upon remission rate, response rate and subour study for unselected cohorts of patients for 1986-sequent outcome. They were predominantly an unselec-1988 (64 patients) 1989-1992 (100 patients) and 1992-ted population based group of patients (other than by 1994 (31 patients) in spite of progressive increases in age) that could be used by purchasers of health care the proportion of patients receiving IFN (respectively 6, as a model for outcome assessment. All patients were 35 and 58%). This is likely to be due to the dilution scheduled to receive a care plan which included a of benefit to specific patients by the overall number of sequential package of treatment consisting initially of patients involved. Outcome data from unselected courses of infusional chemotherapy using vincristine, patients are now expected by purchasers and presented adriamycin and methyl prednisolone (VAMP) and 90 of in this way, help qualify the activity impact of advances these also received cyclophosphamide (C-VAMP).made from research trials for the treatment of popuThirty-eight patients received verapamil in addition to lation-based cancer problems.
C-VAMP(V-C-VAMP). After VAMP all patients wereKeywords: myeloma; induction; autologous transplanplanned to receive high-dose treatment with melphalan tation; interferon; outcome assessment; population based and an autograft (marrow or blood) and 112 received this treatment; a further 29 patients received modified high-dose treatment with melphalan alone (23) or busulfan (6) and 54 (28%) did not proceed to high-dose treatSince 1980, three important and entirely different treatment because of refusal, resistant disease, poor performments for myeloma have been developed in phase II studies ance or treatment-related death. The patients who and then been shown in controlled trials to markedly received melphalan or busulfan alone instead of highimprove outcome for selected patients with myeloma; dose melphalan/autografts did so because of increasing namely infusional induction chemotherapy, 1-3 high-dose age (P = 0.001) and a raised creatinine (P = 0.05). The consolidation chemotherapy 4,5 with autologous bone marcomplete remission rate was 53% for the whole group row rescue, 6,7 and maintenance interferon. 8,9 However, the and 74% for those receiving high-dose melphalan and nature of controlled trials, with strict entry criteria, usually an autograft. From July 1988, the sequential therapy requires that patients are selected, and further selection package in...