Does intensive treatment with high dose chlorambucil and prednisone as first line and cladribine as second line influence the survival of the patients with chronic lymphocytic leukemia?
T. Robak et al., Does intensive treatment with high dose chlorambucil and prednisone as first line and cladribine as second line influence the survival of the patients with chronic lymphocytic leukemia?, LEUK LYMPH, 41(5-6), 2001, pp. 545-557
Cladribine (2-CdA) and fludarabine are the new purine analogs introduced in
the treatment of chronic lymphocytic leukemia (CLL). Despite the high resp
onse rate, their influence on survival is still uncertain. The aim of this
study was a retrospective analysis and comparison of the response rate and
survival of CLL patients treated with high dose chlorambucil (HDChl) as fir
st and 2-CdA as second line, with an historical group of patients never tre
ated with purine analogs who received standard doses of chlorambucil (SDChl
). We analyzed 347 patients with CLL treated between January 1985 and Janua
ry 2000. Group A (190 patients) received HDChl (12 mg/m(2)) with prednisone
(P) 30 mg/m(2) daily for 7 days monthly as first line and in refractory or
early relapsed patients 2-CdA (0.12 mg/kg/day) for 5 days with or without
P (30mg/m(2)) as second line. Group B (157 patients) received continuous SD
Chl (4-8 mg/m(2)/day) and P as first line and COP or CHOP as second line. T
he overall response rate (OR) for the first line was 48,4% in group A and 3
8,9% in group B (p=0.09). 148 patients in group A and 52 in group B receive
d the second line treatment and the second OR was 19.6% and 13.5%, respecti
vely (p=0.4). At the time of analysis, 124 patients died in group A and 139
in group B. Median survival was 65 months and 50 months, respectively. In
group A, survival was longer in advanced Rai stage patients (p=0.001) but i
n early Rai stage was similar for both groups (p=0.4). We suggest that inte
nsive treatment with HDChl as first line and 2-CdA as second line should be
applied in more advanced rather than in less advanced stages of CLL until
the final results of randomized clinical trials are available.