Abrogation of the negative influence of opioids on IL-2 immunotherapy of renal cell cancer by melatonin

Citation
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
Citations number
12
Categorie Soggetti
Urology & Nephrology
Journal title
EUROPEAN UROLOGY
ISSN journal
03022838 → ACNP
Volume
38
Issue
1
Year of publication
2000
Pages
115 - 118
Database
ISI
SICI code
0302-2838(200007)38:1<115:AOTNIO>2.0.ZU;2-W
Abstract
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.