PROGNOSTIC FACTORS IN PURGED MARROW FROM PATIENTS WITH NEUROBLASTOMA RECEIVING MYELOABLATIVE TREATMENT - TUMOR-CELL NUMBER, N-MYC PROTEIN, N-MYC GENE AMPLIFICATION AND RATE OF HEMATOLOGIC RECOVERY
Y. Gazitt et al., PROGNOSTIC FACTORS IN PURGED MARROW FROM PATIENTS WITH NEUROBLASTOMA RECEIVING MYELOABLATIVE TREATMENT - TUMOR-CELL NUMBER, N-MYC PROTEIN, N-MYC GENE AMPLIFICATION AND RATE OF HEMATOLOGIC RECOVERY, International journal of oncology, 3(4), 1993, pp. 755-761
We have previously reported on a study of a small number of patients w
ith advanced neuroblastoma (NBL) receiving myeloablative treatment and
autologous marrow rescue in which occult NBL cells were found in the
marrow of almost every transplanted patient. In addition, we have show
n that the incidence of later relapse correlated better with the N-myc
protein level in the harvested marrow than with the presence of N-myc
gene amplification. We have now analyzed the characteristics of marro
w harvested from 60 patients in remission and correlated survival time
with the following variables: number of NBL cells, expression of N-my
c and c-myc protein, N-myc gene amplification, expression of MDR-1, DN
A index, and rate of the patients' engraftment after myeloablation. Th
e results of this retrospective study indicate a marginally significan
t association between survival time and the level of N-myc protein (p=
0.053) or N-myc gene amplification (p=0.063). On the other hand, the n
umber of NBL cells recovered from the purged marrow was significantly
associated with survival time (p=0.019). Similarly, the number of nucl
eated cells reinfused into the patients (p=0.003), and their rate of e
ngraftment (p=0.008) were strongly associated with survival time. The
expression of c-myc protein and perhaps of MDR-1 protein, and the DNA
index were not associated with survival, in this particular group of p
atients. Prospective studies will be needed to substantiate the result
s of this retrospective study. Detailed evaluation of marrow purgates
harvested from NBL patients undergoing myeloablative treatment and bon
e marrow rescue can potentially provide valuable information on the bi
ology of the disease and may eventually help in the improvement of tre
atment.