Imashuku S, Todo S, Nakajima F
Gan To Kagaku Ryoho. 1983 Sep;10(9):1936-43.
Neuroblastoma, one of the commonest malignant childhood tumors, arises from the adrenal glands and/or sympathetic ganglia, and metastases into lymph nodes, bone marrow, bones, etc. Patients with advanced stages of neuroblastoma are poorly responsive to current combined chemo-radiotherapy. However, neuroblastoma is known to maturate into benign ganglioneuroma spontaneously or induced by certain chemicals. In our previous studies, adenosine 3', 5'-monophosphate (cAMP) was found to play an important role in this maturational process. It was also demonstrated that long-term continuous infusion of dibutyryl cAMP and papaverine caused significant growth-inhibition and tumor differentiation of C 1300 neuroblastoma in mice. These results prompted us to apply intra-aortic PGE1 infusion to two cases of abdominal neuroblastomas with stages III and IV.PGE1 infusion (0.25-3.0 ng/kg/min, over the period of 3 to 32 weeks), combined with oral papaverine and conventional chemotherapy, was effective in decreasing tumor size and promoting tumor maturation in the infused area. However, distant osseous metastases occurred in both cases, during and after the PGE1 administration. Similar modalities should be further evaluated in order to potentiate anti-metastatic effect on neuroblastoma cells.
神经母细胞瘤是儿童最常见的恶性肿瘤之一,起源于肾上腺和/或交感神经节,并转移至淋巴结、骨髓、骨骼等部位。晚期神经母细胞瘤患者对目前的放化疗联合治疗反应不佳。然而,已知神经母细胞瘤可自发成熟为良性神经节细胞瘤,或由某些化学物质诱导成熟。在我们之前的研究中,发现3',5'-环磷酸腺苷(cAMP)在这一成熟过程中起重要作用。还证实,长期持续输注二丁酰cAMP和罂粟碱可导致小鼠C1300神经母细胞瘤显著生长抑制和肿瘤分化。这些结果促使我们对2例III期和IV期腹部神经母细胞瘤患者进行主动脉内输注前列腺素E1(PGE1)治疗。输注PGE1(0.25 - 3.0 ng/kg/分钟,持续3至32周),联合口服罂粟碱和传统化疗,在减小肿瘤大小和促进输注区域肿瘤成熟方面有效。然而,在PGE1给药期间及之后,两例患者均出现远处骨转移。应进一步评估类似方法,以增强对神经母细胞瘤细胞的抗转移作用。