A. Destefani et al., TREATMENT OF ORAL CAVITY AND OROPHARYNX SQUAMOUS-CELL CARCINOMA WITH PERILYMPHATIC INTERLEUKIN-2 - CLINICAL AND PATHOLOGICAL CORRELATIONS, Journal of immunotherapy with emphasis on tumor immunology, 19(2), 1996, pp. 125-133
Citations number
28
Categorie Soggetti
Immunology,Oncology,"Medicine, Research & Experimental
We describe the correlations between the clinical and histologic findi
ngs in an initial series of 60 patients with T2-4, NO-3, MO squamous c
ell carcinoma (SCC) of the oral cavity or oropharynx enrolled in a ran
domized trial set up to evaluate whether the disease-free interval and
survival are extended when perilymphatic injections of recombinant in
terleukin-2 (rIL-2) are combined with routine surgery and radiotherapy
. Twenty-nine patients were operated on only (controls). The other 31
received two daily injections of 2,500 U rIL-2, one near the mastoid p
rocess on the same side as the tumor and the other under the chin, for
10 days before surgery, and further injections on the nonoperated-on
side on a monthly basis for 1 year starting 4 weeks after surgery (or
radiotherapy, where necessary) in an effort to upregulate the immune s
ystem and delay recurrence. Their surgical specimens displayed a signi
ficantly greater inflammatory reaction, larger areas of necrosis, and
more intense sclerosis. The inflammatory tumor infiltration consisted
of eosinophils, plasma cells, and CD25(+) and human leukocyte antigen
(HLA)-DR(+) lymphocytes. However, no correlations were apparent with r
egard to the intensity of necrosis, eosinophil infiltration, and the n
umber of DR(+) cells and the clinical outcome. By contrast, the correl
ation between CD25(+) cells and a significantly longer disease-free su
rvival suggests that induction of T-cell reactivity, and perhaps speci
fic immunity, is the only important aspect of rIL-2-induced antitumor
reactivity.