A. Ballestrero et al., High-dose chemotherapy with tandem autologous transplantation as part of the initial therapy for aggressive non-Hodgkin's lymphoma, INT J ONCOL, 17(5), 2000, pp. 1007-1013
The purpose of the present study was to evaluate the feasibility and the ef
ficacy of employing a high-dose chemotherapy (HDT) regimen with tandem peri
pheral blood progenitor cells (PBPC) supported transplantation in the initi
al treatment of aggressive non-Hodgkin's lymphoma (NHL). HDT was preceded b
y a standard course of conventional dose chemotherapy in 17 out of the 25 p
atients treated, while in 8 cases it was delivered after only one or two cy
cles. HDT was a three-step procedure which included high-dose (6-7 g/m(2))
cyclophosphamide (CY) supported by haematopoietic growth factors, the first
myeloablative course with mitoxantrone (NOV) 60, 75 or 90 mg/m(2) plus mel
phalan (L-PAM) 140-180 mg/m(2) with haematopoietic rescue, and the second m
yeloablative course with etoposide (VP) and carboplatin (CARBO) given at 1.
5 g/m(2) each with haematopoietic rescue. PBPC were collected after CY admi
nistration. Twenty-two patients (88%) completed the HDT, haematological rec
onstitution was rapid and complete at each step and there were no toxic dea
ths. The activity of the treatment was high with a CR rate over 90% in the
entire patient population. The 2-year overall survival (OS) and failure-fre
e survival (FFS) rates of patients in both Age-Adjusted International Progn
ostic Index (A-AIPI) groups 2 and 3 are 79% and the disease-free survival (
DFS) rate for the CRs is 85%. In A-AIPI group 1 the 2-year OS and FFS rates
are both 91%.