The evaluation of the immunobiological changes occuring during IL-2 cancer
immunotherapy is not only Important to correlate them with the clinical res
ponse or to understand the immune mechanism Involved in tumor growth contro
l, but also to predict the efficacy of treatment itself. As far as the immu
ne status of patients prior to therapy is concerned, the evidence of the ac
tivation of the inflammatory response correlates with resistance to IL-2. T
herefore, the evidence of abnormally high pretreatment values of inflammato
ry response markers, including ESR, CRP, neopterin and SIL-2R, may predict
a lack of IL-2 efficacy. In contrast, changes in inflammatory parameters du
ring IL-2 administration have no prognostic significance. The evidence of e
levated pretreatment levers of the immunosuppressive cytokine IL-10 has als
o an unfavourable prognostic significance. At the other side, the evidence
of a marked increase in hemopoietic cells involved in tumor cell destructio
n, such as lymphocytes and eosinophils, as well as in blood levels of antit
umor cytokines, such as IL-12, correlates with efficacy of IL-2 cancer immu
notherapy. A better definition of the prognostic significance of immunoinfl
ammatory markers will allow us to manipulate and improve host biological re
sponse during cancer immunotherapy with IL-2.