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丙型肝炎的治疗:α干扰素再治疗

Therapy of hepatitis C: re-treatment with alpha interferon.

作者信息

Alberti A, Chemello L, Noventa F, Cavalletto L, De Salvo G

机构信息

Department of Clinical and Experimental Medicine, Clinica Medica II, University of Padova, Italy.

出版信息

Hepatology. 1997 Sep;26(3 Suppl 1):137S-142S. doi: 10.1002/hep.510260724.

Abstract

The long-term benefit of interferon therapy in chronic hepatitis C is limited. During therapy, serum alanine aminotransferase (ALT) levels decrease to normal and hepatitis C virus (HCV) RNA decreases in 40% to 60% of patients. However, most patients relapse after therapy withdrawal, so that no more than 15% to 25% achieve a sustained response. Re-treatment has been evaluated in studies using different regimens and forms of alpha interferon in different cohorts of patients at different times after initial therapy. Both end-of-treatment and sustained responses to re-treatment correlate with the type of response achieved during the initial course. Patients who do not respond or have only a partial response to the initial course of interferon have an extremely low rate of sustained response when re-treated, independently of the regimen used. Combining data from 13 studies, sustained responses occurred in no patients who were re-treated with 3 million units (MU) three times weekly for 6 months, and in only 2% to 3% of patients re-treated with higher doses and/or for longer periods. In contrast, a significant number of patients who responded during the initial course but subsequently relapsed have a sustained response when re-treated with interferon alone. Combining data from 11 published studies on patients who relapsed after an initial course, sustained responses occurred in 15% (95% confidence interval [CI], 10%-20%) of patients re-treated with 3 MU three times weekly for 6 months, in 29% (CI, 17%-40%) re-treated with a higher dose for 6 months, and in 43% (CI, 34%/50%) re-treated for at least 12 months. On the other hand, patients who relapsed after a 12-month course of interferon had only 4% rate (range, 0%-8%) of sustained response when re-treated. The best predictor of sustained response to re-treatment in patients who had relapsed was a negative serum HCV-RNA test by polymerase chain reaction at the end of the first course. These results, which have been confirmed in a recent prospective, randomized controlled trial, indicate that nonresponders to interferon should not be re-treated with interferon alone, whereas patients who relapse after a 6-month course of alpha interferon therapy have an indication to be re-treated for at least 12 months, especially if serum HCV RNA was negative at the end of the first course of treatment.

摘要

干扰素疗法对慢性丙型肝炎的长期益处有限。在治疗期间,40%至60%的患者血清丙氨酸氨基转移酶(ALT)水平降至正常,丙型肝炎病毒(HCV)RNA水平下降。然而,大多数患者在治疗停药后复发,因此只有不超过15%至25%的患者能获得持续应答。在不同时间,针对不同患者队列,使用不同方案和形式的α干扰素进行再治疗的研究已得到评估。再治疗的治疗结束时应答和持续应答均与初始疗程所达到的应答类型相关。对初始干扰素疗程无应答或仅有部分应答的患者,再治疗时获得持续应答的几率极低,与所使用的方案无关。综合13项研究的数据,每周三次、每次300万单位(MU)、共治疗6个月的再治疗患者中无一人获得持续应答,而使用更高剂量和/或更长疗程进行再治疗的患者中只有2%至3%获得持续应答。相比之下,大量在初始疗程中有应答但随后复发的患者,单独使用干扰素再治疗时可获得持续应答。综合11项已发表的关于初始疗程后复发患者的研究数据,每周三次、每次300万单位、共治疗6个月的再治疗患者中,15%(95%置信区间[CI],10% - 20%)获得持续应答;使用更高剂量治疗6个月的患者中,29%(CI,17% - 40%)获得持续应答;治疗至少12个月的患者中,43%(CI,34%/50%)获得持续应答。另一方面,接受12个月干扰素疗程后复发的患者,再治疗时获得持续应答的几率仅为4%(范围,0% - 8%)。对复发患者再治疗获得持续应答的最佳预测指标是第一个疗程结束时聚合酶链反应检测血清HCV - RNA呈阴性。这些结果在最近一项前瞻性随机对照试验中得到了证实,表明对干扰素无应答者不应单独使用干扰素进行再治疗,而接受6个月α干扰素治疗后复发的患者有指征进行至少12个月的再治疗,尤其是在第一个疗程结束时血清HCV RNA为阴性的情况下。

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