通过病毒和生化测量对daclatasvir加索非布韦治疗的埃及丙型肝炎患者的反应和无反应进行预测和比较研究

A. El-Gebaly
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引用次数: 0

摘要

世界上大多数肝脏疾病和肝细胞癌(HCC)都是由丙型肝炎病毒感染引起的。近年来开发的新药都很有前景,但患者对这些药物的反应却各不相同。因此,为了尽早发现对SOF/DCV治疗无反应的患者,以节省医疗费用,并指导他们在不浪费时间的情况下进行适当的治疗,我们在治疗期间(第4周)对100例HCV抗体阳性、肝酶升高(平均基线血清ALT(±SD 123±2.7 U/L)、RT-PCR基线355,000 IU/ ml的患者的血液样本进行了HCV RNA和生化检测,所有患者均为乙型肝炎病毒阴性。这些患者接受DAC 60mg /天加Sofosbuvir 400mg /天的治疗,以预测对该治疗的反应程度。此外,在疗程结束后(12周)进行相同的分析,以比较预测值的结果。治疗第4周的结果显示,95%的患者生化分析转移到正常范围,95%的患者病毒载量下降,而在治疗结束时(第12周)98%的患者在完全正常化范围内完全实现生化反应,病毒滴度达到以下检测限。另一方面,其余的患者样本仍然异常,被归类为无反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A PREDICTIVE AND COMPARATIVE STUDY VIA VIRAL AND BIOCHEMICAL MEASUREMENTS FOR RESPONDERS AND NON-RESPONDERS EGYPTIAN HEPATITIS C PATIENTS TO DACLATASVIR PLUS SOFOSBUVIR THERAPY
Most of the liver diseases and hepatocellular carcinoma (HCC) worldwide is due to infection with hepatitis C virus. The developed new drugs in the last few years are promising, but patients response to such drugs are different. Therefore, to identify early the non-responding patients to SOF/DCV therapy for saving of medical costs and to guide them for appropriate treatment without wasting time, HCV RNA in conjunction with biochemical tests were measured during treatment (at week 4) for 100 blood samples from patients were positive for antibodies to (HCV), elevated liver enzymes (mean baseline serum ALT (±SD 123±2.7 U/L), RT-PCR baseline 355,000 IU/ ml. All patients were negative for hepatitis B virus. These patients were under treatment with DAC 60 mg/day plus Sofosbuvir 400 mg/day to give a predictive outcome of the extent of response or not to this therapy. In addition, the same analyses were performed after the end of course therapy (12 weeks) in order to compare the results of the predictive value. The obtained results at  week 4 of treatment indicated that 95% of patients had been shifted to normal range for biochemical analysis measured in addition, viral load was decreased in 95% of patients, while at the end of treatment course (week 12) biochemical response was completely achieved in 98% of patients in a complete normalization ranges  as well as, viral titer reached to the below detection limit. On the other hand, the rest of the patient samples still abnormal and classified as non-responding.
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