P. Lissoni et al., Abrogation of the negative influence of opioids on IL-2 immunotherapy of renal cell cancer by melatonin, EUR UROL, 38(1), 2000, pp. 115-118
IL-2 immunotherapy has been proven to be effective in the treatment of meta
static renal cell cancer (RCC). However, several drugs commonly used in the
palliative therapy of cancer may potentially influence IL-2 efficacy, sinc
e the anticancer immunity has appeared to depend on complex interactions be
tween immune system and psychoneuroimmunomodulation. In particular, experim
ental studies and preliminary clinical investigations have shown that the o
pioid substances, namely morphine, may suppress the anticancer immunity and
the efficacy of IL-2 itself. In contrast, other neuroactive substances, in
particular the pineal hormone melatonin (MLT), have been proven to stimula
te the immune response, including the anticancer immunity, and to abrogate
opioid-induced immunosuppression. On this basis, a study was planned to eva
luate the effect of a concomitant MLT administration on the efficacy of IL-
2 immunotherapy in advanced cancer patients chronically treated with morphi
ne for cancer-related pain. The study was carried out in 30 metastatic RCC
patients under chronic therapy with morphine at oral doses ranging from 60
to 120 mg/day. Patients were randomized to receive morphine alone or morphi
ne plus MLT (20 mg/day orally in the evening). The immunotherapeutic cycle
consisted of IL-2 subcutaneous administration at a dose of 6 million IU/day
for 6 days/week for 4 consecutive weeks. In nonprogressing patients, a sec
ond cycle was planned after a 21-day rest period. The percent of partial re
sponses achieved in patients treated with morphine alone was significantly
lower than that observed in patients concomitantly treated with MLT (1/16 v
s. 4/14, p<0.05). Moreover, the 3-year percent of survival was significantl
y higher in patients concomitantly treated with MLT(p<0.01). In contrast, n
o diminished analgesic efficacy of morphine occurred in patients concomitan
tly treated with MLT. This preliminary study seems to suggest that the nega
tive influence of morphine therapy for cancer-related pain on the clinical
efficacy of IL-2 cancer immunotherapy may be abrogated by the concomitant a
dministration of the immunomodulating pineal neurohormone MLT. Copyright (C
) 2000 S. Karger AG. Basel.