Pl. Zinzani et al., ADULT LYMPHOBLASTIC LYMPHOMA - CLINICAL-FEATURES AND PROGNOSTIC FACTORS IN 53 PATIENTS, Leukemia & lymphoma, 23(5-6), 1996, pp. 577-582
Lymphoblastic lymphoma (LBL) in adult patients is recognized as a part
icular entity in the high-grade non-Hodgkin's lymphoma (HG-NHL) group
with characteristic clinical and prognostic features. Initially, polyc
hemotherapy normally used in HG-NHL failed to produce long-term relaps
e-free survival because of progression disease in the CNS and in the b
one marrow. Subsequently, the intensification of therapy using multimo
dality aggressive acute lymphoblastic leukemia (ALL) treatments led to
an increase in long-term relapse-free survival. We analyzed retrospec
tively 53 adult patients with LBL according to the Kiel classification
and the criteria by Nathwani et al. Therapeutic modifications depende
d upon the different times of diagnosis. Twenty-one patients received
the modified L17 regimen, 13 patients were treated with the L0288 regi
men, and 19 patients were submitted to the L20 protocol. There was no
significant difference in CR rates among the three protocols: 48% vs 5
4% vs 63%, respectively. Nineteen of 29 patients who achieved CR were
alive and relapse free at a median follow-up of 84 months. Ten of the
CR patients underwent autologous bone marrow transplantation (ABMT) to
consolidate the first response and 7 of them are alive and relapse-fr
ee. Early stage of disease, age <30 years, low LDH levels, the absence
of leukemic phase at diagnosis, and, in particular the attainment of
CR were all features of patients with good prognosis. Our study confir
ms the role of intensive polychemotherapeutic regimens including CNS p
rophylaxis, the significance of a score model of prognostic factors, a
nd of the role of ABMT (or allogeneic bone marrow transplantation) in
the treatment of adult LBL.