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dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorManoussakis, M. N.en
dc.contributor.authorGermanidis, Georgios S.en
dc.contributor.authorMoutsopoulos, H. M.en
dc.creatorPavlidis, Nicholasen
dc.creatorManoussakis, M. N.en
dc.creatorGermanidis, Georgios S.en
dc.creatorMoutsopoulos, H. M.en
dc.date.accessioned2018-06-22T09:54:17Z
dc.date.available2018-06-22T09:54:17Z
dc.date.issued1992
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42282
dc.description.abstractThe levels of soluble interleukin‐2 receptors (sIL‐2R) were determined in the serum of 53 patients with B‐cell lymphoproliferative malignancies, including 31 patients with non‐Hodgkin lymphomas (NHL), 16 with chronic lymphocytic leukemia (CLL), and 6 with multiple myeloma. In addition, serum samples from 40 patients with various solid tumors as well as from 53 healthy individuals were used as controls. It was found that the mean serum levels of sIL‐2R were significantly increased (P < 0.001) in NHL (mean ± standard error of the mean 2,327 ± 320 units/ml) and CLL patients (2517 ± 451 units/ml) as compared to normal controls (207 ± 17 units/ml). No such difference was observed when the serum sIL‐2R levels of patients with multiple myeloma or solid tumors were analyzed. Serum sIL‐2R levels were closely related to the clinical stage, the presence of B‐symptoms, and the disease activity of patients with NHL and CLL. In fact, response to chemotherapy was followed by marked decrease or normalization of sIL‐2R levels, while in a number of patients sIL‐2R values were even able to predict disease relapse. Finally, no association with histologic grade in NHL patients, could be demonstrated. We conclude that serum sIL‐2R (1) are increased only in B‐NHL and B‐CLL but not in myeloma patients, (2) are related to the tumor burden, and (3) can serve as a valuable tumor marker for the monitoring of patients treatment. Copyright © 1992 Wiley‐Liss, Inc., A Wiley Companyen
dc.language.isoengen
dc.sourceMedical and pediatric oncologyen
dc.subjectArticleen
dc.subjectAntineoplastic agenten
dc.subjectHumanen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectFemaleen
dc.subjectNeoplasm stagingen
dc.subjectPriority journalen
dc.subjectClinical articleen
dc.subjectLocalen
dc.subjectNeoplasm recurrenceen
dc.subjectNonhodgkin lymphomaen
dc.subjectSolid tumoren
dc.subjectMaleen
dc.subjectInterleukin-2en
dc.subjectLymphomaen
dc.subjectMonoclonal antibodyen
dc.subjectReceptorsen
dc.subjectInterleukin 2 receptoren
dc.subjectTumor markeren
dc.subjectNon-hodgkinen
dc.subjectLeukemiaen
dc.subjectChronicen
dc.subjectLymphocyticen
dc.subjectAcute lymphocytic leukemiaen
dc.subjectB lymphocyteen
dc.subjectCllen
dc.subjectEnzyme linked immunosorbent assayen
dc.subjectMultiple myelomaen
dc.subjectMyelomaen
dc.subjectNhlen
dc.subjectNon-u.s. gov'ten
dc.subjectSil‐2ren
dc.subjectSupporten
dc.titleSerum‐soluble interleukin‐2 receptors in B‐cell lymphoproliferative malignanciesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/mpo.2950200106
dc.description.volume20
dc.description.issue1
dc.description.startingpage26
dc.description.endingpage31
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.contributor.orcidMoutsopoulos, H. M. [0000-0003-3287-4821]
dc.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0003-3287-4821


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