De Groof D, Bruneel H, Musumari T S, Ruppol J F
Med Trop (Mars). 1992 Oct-Dec;52(4):369-75.
The authors report the results of 32 patients with sleeping sickness due to Trypanosoma brucei gambiense treated with DFMO (DL-alpha-difluoromethylornithine), an inhibitor of polyamine biosynthesis. Between those patients, there were 5 new cases, 1 reinfection, and 26 cases with a primary, a secondary resistance or a relapse. 26 cases got DFMO only per os, but six others received first DFMO for two weeks by the intravenous way, followed by three weeks of DFMO per os. The secondary effects were never very severe and never prompted a definitive discontinuation of treatment. 12 cases were followed for a period of 24 months, 16 for a period between 1 and 18 months and 4 patients died during the study (3 during treatment and one 8 months afterwards), but we don't think that DFMO was the cause of death. Out of the 12 cases followed for two years, 11 were in perfect health at the end of this period (one case can be considered as a secondary resistance to DFMO, but it could have been a reinfection as well). For the 16 cases followed for a period less than two years, we found a very fast disappearance of trypanosomes from body fluids, immediately after the beginning of treatment, and a significant amelioration of clinical signs. After this study, the authors estimate that DFMO given orally provides as good results as DFMO given in a combined therapy. But the oral way seems much easier to administer and much cheaper in rural areas.(ABSTRACT TRUNCATED AT 250 WORDS)
作者报告了32例因布氏冈比亚锥虫引起的昏睡病患者接受多胺生物合成抑制剂DFMO(DL-α-二氟甲基鸟氨酸)治疗的结果。在这些患者中,有5例新发病例,1例再次感染,26例为原发性、继发性耐药或复发。26例仅口服DFMO,但另外6例先静脉注射DFMO两周,然后口服DFMO三周。副作用从未非常严重,也从未导致治疗最终中断。12例随访24个月,16例随访1至18个月,4例患者在研究期间死亡(3例在治疗期间,1例在治疗后8个月),但我们认为DFMO不是死亡原因。在随访两年的12例患者中,11例在此期间结束时身体健康(1例可视为对DFMO继发性耐药,但也可能是再次感染)。对于随访时间不到两年的16例患者,我们发现治疗开始后,体液中的锥虫很快消失,临床症状明显改善。经过这项研究,作者估计口服DFMO与联合治疗使用DFMO的效果一样好。但在农村地区,口服方式似乎更容易给药且成本更低。(摘要截取自250字)