Journal of Clinical Oncology, Vol 5, 1262-1274, Copyright © 1987 by American Society of Clinical Oncology
Soluble interleukin-2 receptor levels in patients with undifferentiated and lymphoblastic lymphomas: correlation with survival
DK Wagner, J Kiwanuka, BK Edwards, LA Rubin, DL Nelson and IT Magrath
We have been able to detect soluble interleukin-2 receptors (IL-2R) in
pretreatment sera from 80 patients with undifferentiated lymphoma
(predominantly Burkitt's lymphoma) and lymphoblastic lymphoma. The
demonstration of IL-2R in lymphoma-derived cell lines by
immunoprecipitation and direct staining indicates that IL-2R is synthesized
by the tumor cells. Comparisons were made with two other subject groups: 42
sarcoma patients and 17 normal individuals. The distribution of soluble
IL-2R values for lymphoma patients (geometric mean, 1,132 U/mL) was
significantly greater than that of sarcoma patients (geometric mean, 332
U/mL; P = .0001) or normal individuals (geometric mean, 238 U/mL; P =
.0001). Patients with undifferentiated lymphoma stages B, C, and D had
significantly higher soluble IL-2R values (geometric mean, 1,648 U/mL) than
stages A and AR (geometric mean, 706 U/mL; P = .0001) or lymphoblastic
lymphoma (geometric mean, 826 U/mL; P = .0002). Within the lymphoma group,
the soluble IL-2R level was found to be the most significant prognostic
indicator of disease-free interval and survival when compared with other
previously recognized factors such as histology, stage, bone marrow
involvement at presentation, lactic dehydrogenase (LDH), uric acid (UA),
and age. No factor was significantly associated with response to therapy,
ie, the initial achievement of complete remission (CR) status, although
small numbers of patients with a partial response limit interpretation.
Soluble IL-2R levels were measured serially in two patients and were found
to be elevated at presentation or relapse and to decrease to normal levels
during periods of disease remission. IL-2R appears to reflect tumor burden
and may prove to be a useful and specific marker for lymphoid tumors.

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