Pretreatment serum markers and lymphocyte response to interleukin-2 therapy

Citation
L. Fumagalli et al., Pretreatment serum markers and lymphocyte response to interleukin-2 therapy, BR J CANC, 80(3-4), 1999, pp. 407-411
Citations number
38
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
BRITISH JOURNAL OF CANCER
ISSN journal
00070920 → ACNP
Volume
80
Issue
3-4
Year of publication
1999
Pages
407 - 411
Database
ISI
SICI code
0007-0920(199905)80:3-4<407:PSMALR>2.0.ZU;2-I
Abstract
Lymphocytosis is a marker of subcutaneous interleukin (IL)-2 therapy effica cy, whereas baseline elevated inflammatory indices were noticed in IL-2-res istant disease. The aim of this study was to analyse the relationship betwe en pretreatment circulating values of IL-6, neopterin, sIL-2R, ESR and the changes in lymphocyte number in response to IL-2 administration. Twenty met astatic renal cell cancer patients were treated with subcutaneous IL-2 immu notherapy (6 000 000 IU day(-1) for 6 days per week for 4 weeks); tumour re sponse consisted of partial response (PR) in four patients, stable disease (SD) in eight patients and progressive disease (PD) in eight patients. Abno rmally high pretreatment values of each marker were found as follows. IL-6 in seven patients, neopterin in nine patients, sIL-2R in 13 patients, In re sponse to IL-2 immunotherapy, a significantly higher mean increase in lymph ocyte number and a higher percentage of patients with tumour response or st able disease were observed when pretreatment values of IL-6, neopterin and sIL-2R were within the normal range, in comparison to patients with high va lues for these markers. The pretreatment excess of these serum inflammatory markers seems to negatively influence both the host and tumour response to IL-2 administration, by preventing the IL-2-induced lymphocytosis and resu lting in tumour progression, Further studies are requested to verify ii ove rall survival and quality of life may depend on pretreatment host immune st atus and/or lymphocyte response after IL-2 administration.