Awachana Jiamsakul, Iskandar Azwa, Fujie Zhang, Evy Yunihastuti, Rossana Ditangco, Nagalingeswaran Kumarasamy, Oon Tek Ng, Yu-Jiun Chan, Penh Sun Ly, Jun Yong Choi, Man-Po Lee, Sanjay Pujari, Sasisopin Kiertiburanakul, Romanee Chaiwarith, Tuti Parwati Merati, Shashikala Sangle, Suwimon Khusuwan, Benedict Lh Sim, Anchalee Avihingsanon, Cuong Duy, Junko Tanuma, Jeremy Ross, Matthew Law, Treat Asia Hiv Observational Database Of IeDEA Asia-Pacific
{"title":"Treatment modification after second-line failure among people living with HIV in the Asia-Pacific.","authors":"Awachana Jiamsakul, Iskandar Azwa, Fujie Zhang, Evy Yunihastuti, Rossana Ditangco, Nagalingeswaran Kumarasamy, Oon Tek Ng, Yu-Jiun Chan, Penh Sun Ly, Jun Yong Choi, Man-Po Lee, Sanjay Pujari, Sasisopin Kiertiburanakul, Romanee Chaiwarith, Tuti Parwati Merati, Shashikala Sangle, Suwimon Khusuwan, Benedict Lh Sim, Anchalee Avihingsanon, Cuong Duy, Junko Tanuma, Jeremy Ross, Matthew Law, Treat Asia Hiv Observational Database Of IeDEA Asia-Pacific","doi":"10.3851/IMP3388","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The World Health Organization recommends continuation with the failing second-line regimen if third-line option is not available. We investigated treatment outcomes among people living with HIV in Asia who continued with failing second-line regimens compared with those who had treatment modifications after failure.</p><p><strong>Methods: </strong>Treatment modification was defined as a change of two antiretrovirals, a drug class change or treatment interruption (TI), all for >14 days. We assessed factors associated with CD4 changes and undetectable viral load (UVL <1,000 copies/ml) at 1 year after second-line failure using linear and logistic regression, respectively. Survival time was analysed using competing risk regression.</p><p><strong>Results: </strong>Of the 328 patients who failed second-line ART in our cohorts, 208 (63%) had a subsequent treatment modification. Compared with those who continued the failing regimen, the average CD4 cell increase was higher in patients who had a modification without TI (difference =77.5, 95% CI 35.3, 119.7) while no difference was observed among those with TI (difference =-5.3, 95% CI -67.3, 56.8). Compared with those who continued the failing regimen, the odds of achieving UVL was lower in patients with TI (OR=0.18, 95% CI 0.06, 0.60) and similar among those who had a modification without TI (OR=1.97, 95% CI 0.95, 4.10), with proportions of UVL 60%, 22% and 75%, respectively. Survival time was not affected by treatment modifications.</p><p><strong>Conclusions: </strong>CD4 cell improvements were observed in those who had treatment modification without TI compared with those on the failing regimen. When no other options are available, maintaining the same failing ART combination provided better VL control than interrupting treatment.</p>","PeriodicalId":8364,"journal":{"name":"Antiviral Therapy","volume":"25 7","pages":"377-387"},"PeriodicalIF":2.3000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275121/pdf/nihms-1717472.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Antiviral Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3851/IMP3388","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 1
Abstract
Background: The World Health Organization recommends continuation with the failing second-line regimen if third-line option is not available. We investigated treatment outcomes among people living with HIV in Asia who continued with failing second-line regimens compared with those who had treatment modifications after failure.
Methods: Treatment modification was defined as a change of two antiretrovirals, a drug class change or treatment interruption (TI), all for >14 days. We assessed factors associated with CD4 changes and undetectable viral load (UVL <1,000 copies/ml) at 1 year after second-line failure using linear and logistic regression, respectively. Survival time was analysed using competing risk regression.
Results: Of the 328 patients who failed second-line ART in our cohorts, 208 (63%) had a subsequent treatment modification. Compared with those who continued the failing regimen, the average CD4 cell increase was higher in patients who had a modification without TI (difference =77.5, 95% CI 35.3, 119.7) while no difference was observed among those with TI (difference =-5.3, 95% CI -67.3, 56.8). Compared with those who continued the failing regimen, the odds of achieving UVL was lower in patients with TI (OR=0.18, 95% CI 0.06, 0.60) and similar among those who had a modification without TI (OR=1.97, 95% CI 0.95, 4.10), with proportions of UVL 60%, 22% and 75%, respectively. Survival time was not affected by treatment modifications.
Conclusions: CD4 cell improvements were observed in those who had treatment modification without TI compared with those on the failing regimen. When no other options are available, maintaining the same failing ART combination provided better VL control than interrupting treatment.
背景:世界卫生组织建议,如果没有三线方案,则继续使用失败的二线方案。我们调查了亚洲继续使用失败的二线治疗方案的艾滋病病毒感染者的治疗结果,与失败后修改治疗方案的患者进行了比较。方法:治疗改变定义为两种抗逆转录病毒药物的改变,药物类别的改变或治疗中断(TI),均大于14天。我们评估了与CD4变化和无法检测到的病毒载量相关的因素(UVL)。结果:在我们的队列中,328名二线抗逆转录病毒治疗失败的患者中,208名(63%)患者随后进行了治疗修改。与继续失败方案的患者相比,没有TI的患者的平均CD4细胞增加更高(差异=77.5,95% CI 35.3, 119.7),而有TI的患者没有差异(差异=-5.3,95% CI -67.3, 56.8)。与继续失败方案的患者相比,有TI的患者实现UVL的几率较低(OR=0.18, 95% CI 0.06, 0.60),而没有TI的患者实现UVL的几率相似(OR=1.97, 95% CI 0.95, 4.10), UVL的比例分别为60%,22%和75%。生存时间不受治疗改变的影响。结论:与失败的治疗方案相比,在没有TI的治疗方案中观察到CD4细胞的改善。当没有其他选择时,维持同样失败的抗逆转录病毒治疗组合比中断治疗提供更好的VL控制。
期刊介绍:
Antiviral Therapy (an official publication of the International Society of Antiviral Research) is an international, peer-reviewed journal devoted to publishing articles on the clinical development and use of antiviral agents and vaccines, and the treatment of all viral diseases. Antiviral Therapy is one of the leading journals in virology and infectious diseases.
The journal is comprehensive, and publishes articles concerning all clinical aspects of antiviral therapy. It features editorials, original research papers, specially commissioned review articles, letters and book reviews. The journal is aimed at physicians and specialists interested in clinical and basic research.