Befon S, Mystakidou K, Lyra M, Tubanakis N, Vlahos L
Pain Relief and Palliative Care Unit, Areteion Hospital, University of Athens, Vas. Sofias 76, 11528, Athens, Greece.
Anticancer Res. 2000 Sep-Oct;20(5C):4039-46.
Somatostatin is a naturally occurring hormone widely identified in a number of human tissues, with a broad spectrum of physiological actions. Octreotide is a synthetic analogue of somatostatin, which seems to be promising in clinical use.
a. to evaluate the efficacy of octreotide in pain control of patients with advanced gastrointestinal cancer, as well as octreotide's outcome in the hepatic function; b. to investigate the relationship between pain intensity and beta-endorphin blood levels in the patients.
The study group consisted of 25 patients (age range: 48-89 years, 14 males, 11 females) with far advanced gastrointestinal cancer.
All the patients were under s.c. morphine administration using a continuous infusion pump. When pain intensity increased, 0.6 mg/day of octreotide was added to the therapeutic regimen in the same syringe of the continuous infusion pump. Pain intensity and beta-endorphin blood levels were measured five times: Once before octreotide administration and the other four 12, 24, 48 hours and 7 days after. A complete blood count and a biochemical screening profile were taken before the administration of octreotide as well as on the 7th and the 14th day.
24 out of 25 cases showed a reduction in pain intensity (pretreatment x = 5.3, post-treatment x = 0.6). beta-endorphin blood levels increased significantly during the study (an increase of 184.78% was observed on the 7th treatment day). In one patient pain control was achieved by increasing morphine dosage. Statistically significant changes were observed in hepatic function indices (p < 0.02). Significant side-effects were not observed.
Octreotide can be used as an adjuvant analgesic in the management of gastrointestinal cancer pain which is managed by continuous s.c. administration. Although fuither research needs to be done, octreotide's administration seemed to improve hepatic function of these patients, therefore, it could potentially have a positive effect in the patient's quality of life.
生长抑素是一种在多种人体组织中广泛存在的天然激素,具有广泛的生理作用。奥曲肽是生长抑素的合成类似物,在临床应用中似乎很有前景。
a. 评估奥曲肽对晚期胃肠道癌患者疼痛控制的疗效以及奥曲肽对肝功能的影响;b. 研究患者疼痛强度与血液中β-内啡肽水平之间的关系。
研究组由25例(年龄范围:48 - 89岁,男性14例,女性11例)晚期胃肠道癌患者组成。
所有患者均通过持续输注泵皮下注射吗啡。当疼痛强度增加时,在持续输注泵的同一注射器中,将0.6毫克/天的奥曲肽添加到治疗方案中。测量疼痛强度和血液中β-内啡肽水平5次:一次在奥曲肽给药前,另外4次分别在给药后12、24、48小时和7天。在奥曲肽给药前以及第7天和第14天进行全血细胞计数和生化筛查。
25例中有24例疼痛强度降低(治疗前x = 5.3,治疗后x = 0.6)。研究期间血液中β-内啡肽水平显著升高(在治疗第7天观察到升高184.78%)。1例患者通过增加吗啡剂量实现了疼痛控制。肝功能指标有统计学意义的变化(p < 0.02)。未观察到明显的副作用。
奥曲肽可作为辅助镇痛药用于通过持续皮下给药治疗的胃肠道癌疼痛管理。尽管需要进一步研究,但奥曲肽的给药似乎改善了这些患者的肝功能,因此,它可能对患者的生活质量产生积极影响。