D. Cunningham et al., A RANDOMIZED TRIAL OF MAINTENANCE INTERFERON FOLLOWING A HIGH-DOSE CHEMOTHERAPY IN MULTIPLE-MYELOMA - LONG-TERM FOLLOW-UP RESULTS, British Journal of Haematology, 102(2), 1998, pp. 495-502
High-dose chemotherapy (melphalan) with autologous marrow stem cell su
pport (AMSCS) results in high response rates in multiple myeloma (MM),
with up to 50% of patients achieving complete remission, However, the
se remissions are generally not durable, As the cytokine interferon al
pha has been shown to prolong partial response following conventional
chemotherapy, this trial was conducted to evaluate its role following
high-dose chemotherapy, 85 patients were randomly assigned to maintena
nce treatment with interferon alpha, 3x10(6) units/m(2) subcutaneously
three times weekly until relapse or no further treatment following re
covery from high-dose chemotherapy (melphalan 140-200mg/m(2) or busulp
han 16 mg/kg) combined with AMSCS, At 5.8 years following the accrual
of the last patient in this trial, 38 patients had died, 17 in the int
erferon arm and 21 in the control arm. The median progression-free sur
vival (PFS) in the 42 patients randomized to interferon alpha was 46 m
onths versus 27 months in the controls. Both overall survival and PFS,
which were highly significant at median follow-up of 52 months, have
now ceased tc, be significant, because most patients have ultimately s
uccumbed to their disease, Interferon was tolerated by the majority of
patients with very good compliance. Toxicity consisted mainly of flu-
like symptoms and malaise which were usually self-limiting. The result
s of such a pilot study should be carefully interpreted and the benefi
ts of interferon should be confirmed in larger multicentre studies in
the setting of minimal residual disease following autologous transplan
tation.