J. Fleury et al., HIGH-DOSE THERAPY AND AUTOLOGOUS BONE-MARROW TRANSPLANTATION IN FIRSTCOMPLETE OR PARTIAL REMISSION FOR POOR-PROGNOSIS HODGKINS-DISEASE, Leukemia & lymphoma, 20(3-4), 1996, pp. 259-266
We report the experience of three French centres which evaluated high-
dose therapy (HDT) as consolidation therapy for poor prognosis Hodgkin
's disease (HD). From March 1986 to April 1990, 23 consecutive patient
s with poor prognosis stage IV HD underwent HDT followed by autologous
bone marrow transplantation (AB MT) after achieving either complete r
emission (CR 1) or good partial response (GPR1) (reduction mass > 75%)
. The median age was 31 years (range 18 to 55 years), 14 were male. Ai
l patients except one initially had at least 2 poor prognosis factors
such as: systemic symptoms (n = 19), bulky tumor (n = 16), more than o
ne extranodal site (n = 9), bone marrow involvement (n = 5), lymphocyt
e count less than or equal to 1.10(9)/1 (n = 8) and biological stage b
(n = 21). All patients had previously been treated with alternating M
OPP/ABVD. Ten patients were in GPR1 and 13 in CR1 before transplant. T
he conditioning regimens were: CBV (n = 17), BEAM (n = 5), BEAC (n = 1
) followed by bone marrow rescue. Radiotherapy was introduced just bef
ore the conditioning regimen for 6 patients or after ABMT for 5 patien
ts. Nine of 10 patients in GPR1 achieved CR after ABMT but one died ea
rly of treatment-related toxicity. Five of 22 patients who were in CR
posttransplant, relapsed (3, 4, 4, 18, 36 months). Seventeen patients
remain alive in continuous CR with a median follow-up of 60 months (ra
nge: 30-100 months). The overall survival (OS) and disease-free surviv
al (DFS) projected at 5 years are 92% and 77% respectively. Consolidat
ion by HDT and ABMT proved to be well tolerated. An international tria
l is currently underway to attempt to demonstrate a clear benefit on s
urvival for this subset of poor prognosis HD patients.