Long-term follow-up results of adult patients with acute lymphocytic leukemia or lymphoblastic lymphoma treated with short-term, alternating non-cross-resistant chemotherapy: Japan Clinical Oncology Group Study 8702
T. Kobayashi et al., Long-term follow-up results of adult patients with acute lymphocytic leukemia or lymphoblastic lymphoma treated with short-term, alternating non-cross-resistant chemotherapy: Japan Clinical Oncology Group Study 8702, JPN J CLIN, 29(7), 1999, pp. 340-348
Background: Patients with acute lymphocytic leukemia (PILL) and those with
lymphoblastic lymphoma (LBL) have overlapping clinical and immunophenotypic
features and they have been treated with the same or very similar chemothe
rapy regimens. The goal of this multi-institutional phase II trial waste ev
aluate the therapeutic efficacy of a short-term, six-drug chemotherapy regi
men for adult patients with untreated ALL or LBL.
Methods: Forty-six eligible patients, 41 with ALL and five with LBL, were t
reated with a short-term (planned total therapy duration; 36-38 weeks), sim
plified chemotherapy program; two courses of VEPA-L (vincristine, cyclophos
phamide, prednisolone, doxorubicin, I-asparaginase plus intrathecal methotr
exate and prednisolone) followed by four courses of M-VEPA (methotrexate pl
us VEPA), without the traditional maintenance therapy using daily 6-mercapt
opurine and weekly methotrexate.
Results: Thirty-six (78%; 95% confidence interval 64-89%) of the 46 eligibl
e patients achieved complete remission (CR). Among the 36 patients who achi
eved CR, four (11%) died of treatment complications, 26 (72%) relapsed and
six (17%) remain alive in continuous CR. The median survival for all 46 eli
gible patients is 14 months and the median disease-free survival (DFS) for
the 36 patients who achieved CR is II months. The estimate of the proportio
n of survival at 7 years of all 46 eligible patients is 15% at-a median fol
low-up time of 96 months and that of DFS of the. 36 patients achieving CR i
s 17% at a median follow-up time of 93 months. Subgroup analysis showed tha
t an elevated serum C-reactive protein (CRP) level, age of 30 years or olde
r, the. presence of B-symptom and T-cell phenotype were likely to be associ
ated with shortened survival. Although the observed CR rate (78%) is within
the range of satisfaction, the long-term survival rate (15%) is inferior t
o those of published programs incorporating maintenance therapy.
Conclusions: A fraction of-adult patients with ALL or LBL are curable with
a short-term, six-drug chemotherapy regimen. However, this simplified thera
py of shorter duration cannot be recommended.