Study objectives: To evaluate the usefulness of measuring sIL2R for diagnos
tic and prognostic purposes and for monitoring disease during a 6-month per
iod of chemotherapy, and to investigate the clinical significance of sIL2R
serum concentrations. Methods: The serum concentration of sIL2R, TPA and ly
mphocyte subsets CD4, CD8, CD25, CD16 were measured at diagnosis and then 1
and 6 months after the start of chemotherapy. Patients: There were 39 pati
ents (three females, 36 males; mean age 61.6 years) with lung cancer (LC),
treated with chemotherapy and 22 control subjects (six females, 16 males; m
ean age 50.1 years) with non-neoplastic lung diseases. Results: No signific
ant differences in sIL2R serum concentrations were observed at diagnosis be
tween the control and LC group or when comparing the different histotypes,
disease stages (IIIa-b vs IV) and survival (survival less than or equal to
12 vs > 12 months). On comparing the sequential variations of the examined
parameters a significant increase in sIL2R; (P < 0.007) after 1 and 6 month
s versus basal value was observed only in patients surviving less than 12 m
onths and in those who did not respond to chemotherapy. Moreover a negative
correlation was observed between sIL2R serum concentrations and CD25 + and
CD16 + lymphocyte subsets. Evaluation of survival curves of patients with
basal sIL2R > or less than or equal to 700 U/ml showed a slightly lower sur
vival rate in the former group. Conclusions: The present results, confirmin
g the poor utility of sIL2R in the diagnostic phase of the disease, show it
s usefulness in prognostic evaluation and in the clinical surveillance of p
atients with advanced lung cancer submitted to polychemotherapy. In this ca
se any variations in sIL2R serum levels are likely to relate to the spread
of the neoplasia rather than to the host immune response. (C) 1999 Elsevier
Science Ireland Ltd. All rights reserved.