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艾滋病患者的巨细胞病毒性食管炎:对更昔洛韦治疗的临床反应、复发率及长期预后的前瞻性评估

Cytomegalovirus esophagitis in AIDS: a prospective evaluation of clinical response to ganciclovir therapy, relapse rate, and long-term outcome.

作者信息

Wilcox C M, Straub R F, Schwartz D A

机构信息

Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30303.

出版信息

Am J Med. 1995 Feb;98(2):169-76. doi: 10.1016/s0002-9343(99)80400-8.

Abstract

PURPOSE

Although cytomegalovirus (CMV) esophagitis is an important complication of acquired immunodeficiency syndrome, there has been little study specifically addressing the response to currently available antiviral therapy, relapse rate without maintenance therapy, and long-term outcome.

PATIENTS AND METHODS

Over a 45-month period, 44 patients with CMV esophagitis established endoscopically and histopathologically were prospectively identified from among all human immunodeficiency virus (HIV)-infected patients undergoing endoscopy. Induction therapy consisted of intravenous ganciclovir at 10 mg/kg per day for approximately 14 days. Foscarnet was given at 60 mg/kg every 8 hours for nonresponders to ganciclovir.

RESULTS

Of these patients, 35 completed induction ganciclovir therapy, resulting in a complete response in 17 (49%) and a partial response in 10 (29%), yielding a 77% overall response rate. Seven of 8 nonresponders were subsequently treated with foscarnet, with a clinical response seen in 5 patients. In the 18 eventual complete responders to ganciclovir or foscarnet followed up without maintenance therapy, 7 (39%) relapsed at a median of 4 months (range 2 to 18 months). In all cases, relapse was manifested by recurrent odynophagia. Reinduction ganciclovir therapy yielded a complete response in 1 patient and a partial response in 2, and induction foscarnet treatment resulted in a complete response in the other treated patients. During long-term follow-up, 1 complete responder developed CMV colitis with concurrent retinitis, and 4 other patients developed retinitis. The median survival after diagnosis was 8.2 months, although survival for greater than 1 year was seen in 4 patients. No patient died as a direct result of esophageal disease, although ulcer-related bleeding may have contributed to death in 2 patients with end-stage liver diseases and hepatic encephalopathy.

CONCLUSIONS

CMV esophagitis has a favorable response to induction ganciclovir therapy, and a long-term remission may occur after induction therapy alone. Despite the favorable response to ganciclovir therapy, the long-term survival is poor, reflecting the severe immunodeficiency of these patients.

摘要

目的

尽管巨细胞病毒(CMV)食管炎是获得性免疫缺陷综合征的重要并发症,但针对目前可用抗病毒治疗的反应、无维持治疗时的复发率以及长期预后的专门研究较少。

患者与方法

在45个月期间,从所有接受内镜检查的人类免疫缺陷病毒(HIV)感染患者中前瞻性地确定了44例经内镜和组织病理学确诊为CMV食管炎的患者。诱导治疗包括静脉注射更昔洛韦,剂量为每日10mg/kg,持续约14天。对于对更昔洛韦无反应者,每8小时给予膦甲酸钠60mg/kg。

结果

这些患者中,35例完成了更昔洛韦诱导治疗,17例(49%)完全缓解,10例(29%)部分缓解,总体缓解率为77%。8例无反应者中的7例随后接受了膦甲酸钠治疗,5例出现临床反应。在18例最终对更昔洛韦或膦甲酸钠完全缓解且未接受维持治疗的患者中,7例(39%)复发,中位复发时间为4个月(范围2至18个月)。所有病例中,复发均表现为复发性吞咽痛。再次诱导更昔洛韦治疗使1例患者完全缓解,2例部分缓解,诱导膦甲酸钠治疗使其他接受治疗的患者完全缓解。在长期随访中,1例完全缓解者发生了CMV结肠炎并伴有视网膜病变,另外4例患者发生了视网膜病变。诊断后的中位生存期为8.2个月,尽管4例患者生存期超过1年。没有患者因食管疾病直接死亡,尽管溃疡相关出血可能导致2例终末期肝病和肝性脑病患者死亡。

结论

CMV食管炎对更昔洛韦诱导治疗反应良好,单独诱导治疗后可能出现长期缓解。尽管对更昔洛韦治疗反应良好,但长期生存率较低,反映了这些患者严重的免疫缺陷。

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