大剂量松果体激素褪黑素对淋巴细胞减少性无法治疗的转移性癌症患者淋巴细胞-单核细胞比率改善动力学的2期研究

Lissoni Paolo, Porro Giorgio, Cenaj Vezika, Aymerich Tiziana, Lissoni Arianna, Di Fede Giuseppe
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引用次数: 0

摘要

众所周知,淋巴细胞减少症是癌症患者最负性的生物标志物之一,是癌症相关免疫抑制的一种表达。目前已知抗肿瘤免疫虽然复杂,但主要由树突状细胞-T淋巴细胞系统介导,并受巨噬细胞调节性T淋巴细胞系统抑制。因此,淋巴细胞与单核细胞比率(LMR)已被证明是比单纯的淋巴细胞减少症更合适的预后临床指标。由于淋巴细胞在介导肿瘤细胞破坏中的基础性作用,肿瘤相关性淋巴细胞减少症的纠正可影响肿瘤疾病的临床病史。目前,在体内唯一能明确诱导淋巴细胞凋亡的细胞因子是IL-2。然而,已经证明免疫系统在生理上是受神经内分泌控制的,松果体激素MLT可能刺激T淋巴细胞的增殖和活化。在此基础上,我们评估了高剂量MLT治疗持续性淋巴细胞减少和LMR异常低值转移性实体瘤患者的效果。该研究包括14名患者,结果与对照组的20名淋巴细胞减少性无法治疗的转移性癌症患者进行了比较,这些患者仅接受了最好的支持治疗。患者接受MLT治疗,剂量为100mg /天,晚间口服,连续3个月。MLT治疗后淋巴细胞平均计数增加,治疗2个月后淋巴细胞计数明显高于治疗前,4/14(29%)患者淋巴细胞计数恢复正常,而对照组淋巴细胞无自发升高。另一方面,单核细胞计数在MLT治疗后迅速减少,治疗仅一个月后观察到的LMR平均值显著高于治疗前,而对照组则显著降低。本初步研究表明,大剂量MLT可改善肿瘤患者的免疫状态,可有效治疗弥漫性肿瘤相关淋巴细胞减少症。
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A Phase-2 Study on the Kinetics of the Improvement in Lymphocyte-toMonocyte Ratio by High-Dose Pineal Hormone Melatonin in Lymphocytopenic Untreatable Metastatic Cancer Patients
It is known that lymphocytopenia is one of the most negative biomarkers in cancer patients, being an expression of cancer-related immunosuppression. Today it is known that, despite its complexity, the antitumor immunity is mainly mediated by dendritic cell-T lymphocyte system and suppressed by the macrophage-regulatory T lymphocyte system. Then, lymphocyte-to-monocyte ratio (LMR) has been proven to represent a more appropriate prognostic clinical index than the simple lyphocytopenia alone. Because of the fundamental role of lymphocytes in mediating tumor cell destruction, the correction of cancer-related lymphocytopenia could influence the clinical history of the neoplastic disease. At present, the only cytokine able to induce a clear in vivo lymphocytosisis IL-2. However, it has been demonstrated that the immune system is physiologically under a neuroendocrine control, and that the pineal hormone MLT may stimulate T lymphocyte proliferation and activation. On these bases, we have evaluated the effect of highdose MLT therapy in metastatic solid tumor patients with persistent lymphocytopenia and abnormally low values of LMR. The study included 14 patients, and the results were compared to those found in a control group of 20 lymphocytopenic untreatable metastatic cancer patients treated with the only best supportive care alone. Patients received MLT at a dose of 100 mg/day orally in the evening for 3 consecutive months. Lymphocyte mean count increases on MLT therapy, and the values observed after two months of therapy were significantly higher than the pretreatment ones, with a normalization of lymphocyte number in 4/14 (29%) patients, whereas no spontaneous lymphocyte rise occurred in the control group. On the other hand, monocyte count rapidly diminished on MLT therapy, and LMR mean values observed after only one month of treatment was significantly higher than that found prior to therapy, whereas it significantly decreases in controls. This preliminary study shows that high-dose MLT may improve the immune status of cancer patients, and be effective in the treatment of disseminated cancer-related lymphocytopenia.
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