Am. Gianni et al., HIGH-DOSE SEQUENTIAL CHEMORADIOTHERAPY WITH PERIPHERAL-BLOOD PROGENITOR-CELL SUPPORT FOR RELAPSED OR REFRACTORY HODGKINS-DISEASE - A 6-YEARUPDATE, Annals of oncology, 4(10), 1993, pp. 889-891
Background: Very few studies using high-dose therapy and autologous bo
ne marrow transplantation have a long (i.e., >3 years) follow-up. We r
eport here the 6-year update of a study employing high-dose sequential
chemo-radiotherapy in 25 patients with poor-risk Hodgkin's disease. P
atients and methods: All patients were either refractory (7 patients)
or partial responders (9 patients) or early relapses (9 patients) foll
owing induction chemotherapy consisting of MOPP/ABVD in 20 patients an
d MOPP/ABVD followed by salvage CEP for the remaining 5 patients. The
high-dose chemo-radiotherapy regimen employed consisted in the rapid s
equential administration of high-doses of cyclophosphamide, methotrexa
te, etoposide and total body irradiation plus melphalan. Results: As c
ompared to 4-year results, the 6-year probabilities of relapse-free su
rvival, freedom from progression and overall survival were almost supe
rimposable. In fact, during the two additional years elapsed since pri
or survey, only one event occurred (fatal cerebral hemorrhage) that wa
s unrelated to Hodgkin's disease. In particular, the proportion of pat
ients remaining event-free was 78% for those with short initial comple
te response and 31% for patients who had failed initial MOPP/ABVD. Acc
ording to previous experience, both groups have a very low or no chanc
e of long-term event-free survival when treated with standard-dose sal
vage chemotherapy. Conclusions: The very favorable long-term results o
f the high-dose sequential regimen together with its excellent tolerab
ility and lack of early or late fatal toxicities, will assist clinicia
ns in defining optimal timing for high-dose therapy in the management
of Hodgkin's disease. According to a revised cost/benefit analysis, it
would appear that, at present, the best timing of high-dose sequentia
l therapy in patients failing MOPP/ABVD is at first early relapse.