T. Lerede et al., THERAPEUTIC IMPACT OF ADULT-TYPE ACUTE LYMPHOBLASTIC-LEUKEMIA REGIMENS IN B-CELL L(3) ACUTE-LEUKEMIA AND ADVANCED-STAGE BURKITTS-LYMPHOMA/, Haematologica, 81(5), 1996, pp. 442-449
Background. Adult B/L(3)-ALL is a rare disease subset characterized by
an aggressive clinical course and a poor response to conventional adu
lt ALL-type chemotherapy. Recent data from the GMALL Group showed that
prognosis can be improved with an innovative treatment regimen. In th
e current retrospective survey we focus on therapeutic results obtaine
d at our Institutions during a 15-year period with ALL-type regimens i
n 34 adults with either B/L(3)-ALL or advanced-stage Burkitt's lymphom
a. Methods. Five successive ALL treatment programs were developed. The
y included a homogeneous induction phase with early intrathecal chemop
rophylaxis, multidrug postremission consolidation followed by cranial
irradiation (4 trials), high-dose chemotherapy plus autografting (2 tr
ials), late consolidation (2 trials), and variable-length maintenance
(4 trials). Early response and prolonged disease-free survival rates w
ere analyzed according to selected clinical and therapeutic variables.
Results. Overall, a complete remission was achieved in 62%, with a me
dian duration of 1.6 years and a 10-year remission rate of 49%. A diag
nosis of B/L(3)-ALL (p=0.007), the use of idarubicin instead of adriam
ycin during induction (p=0.018), a serum creatinine <1.6 mg/dL, and an
uninvolved central nervous system were associated with higher respons
e rates. As regards long-term disease-free survival, results were sign
ificantly better in patients with <1 x 10(9)/L L(3)/blast cells in the
peripheral blood (p=0.0029) and/or aged <50 years (p=0.04), and in th
ose consolidated with the most recent rotational high-dose plus periph
eral blood stem cell autotransplant regimen. Conclusions. According to
the results presented, ALL-Like regimens may still represent a worthw
hile therapeutic choice. The use of idarubicin during induction, the p
rognostic subclassification of patients, a careful control of dysmetab
olic complications, the selection of the proper chemo-radioprevention
for meningeal disease and perhaps the introduction of high-dose chemot
herapy supported by autologous stem cell rescue appear to be the mains
tay of further improvements.