Brennan Alana T, Davies Mary-Ann, Bor Jacob, Wandeler Gilles, Stinson Kathryn, Wood Robin, Prozesky Hans, Tanser Frank, Fatti Geoffrey, Boulle Andrew, Sikazwe Izukanji, Wool-Kaloustian Kara, Yuannoutsos Constantin, Leroy Valériane, de Rekeneire Nathalie, Fox Matthew P
aDepartment of Global Health, Boston University, Boston, Massachusetts, USA bHealth Economics and Epidemiology Research Office, Department of Internal Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa cDepartment of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA dCentre for Infectious Disease Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa eDepartment of Infectious Diseases, Bern University Hospital, University of Bern fInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland gThe Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town hDivision of Infectious Diseases, Department of Medicine, University of Stellenbosch & Tygerberg Academic Hospital, Cape Town iAfrica Center for Health and Population Studies, University of Kwazulu-Natal jKheth'Impilo AIDS Free Living, Cape Town kDepartment of Health, Provincial Government of the Western Cape, Cape Town, South Africa lCenter for Infectious Disease Research in Zambia, Lusaka, Zambia mIndiana University School of Medicine, Indianapolis nRichard M. Fairbanks School of Public Health, Indiana University, Indianapolis, Indiana, USA oINSERM U1027, Université Paul Sabatier Toulouse 3, Toulouse pUniversité Bordeaux, ISPED, Centre INSERM U1219 Epidémiologie-Biostatistique, Bordeaux, France.
AIDS. 2017 Jan 2;31(1):147-157. doi: 10.1097/QAD.0000000000001307.
We assessed the relationship between phasing out stavudine in first-line antiretroviral therapy (ART) in accordance with WHO 2010 policy and single-drug substitutions (SDS) (substituting the nucleoside reverse transcriptase inhibitor in first-line ART) in sub-Saharan Africa.
Prospective cohort analysis (International epidemiological Databases to Evaluate AIDS-Multiregional) including ART-naive, HIV-infected patients aged at least 16 years, initiating ART between January 2005 and December 2012. Before April 2010 (July 2007 in Zambia) national guidelines called for patients to initiate stavudine-based or zidovudine-based regimen, whereas thereafter tenofovir or zidovudine replaced stavudine in first-line ART.
We evaluated the frequency of stavudine use and SDS by calendar year 2004-2014. Competing risk regression was used to assess the association between nucleoside reverse transcriptase inhibitor use and SDS in the first 24 months on ART.
In all, 33 441 (8.9%; 95% confience interval 8.7-8.9%) SDS occurred among 377 656 patients in the first 24 months on ART, close to 40% of which were amongst patients on stavudine. The decrease in SDS corresponded with the phasing out of stavudine. Competing risks regression models showed that patients on tenofovir were 20-95% less likely to require a SDS than patients on stavudine, whereas patients on zidovudine had a 75-85% decrease in the hazards of SDS when compared to stavudine.
The decline in SDS in the first 24 months on treatment appears to be associated with phasing out stavudine for zidovudine or tenofovir in first-line ART in our study. Further efforts to decrease the cost of tenofovir and zidovudine for use in this setting is warranted to substitute all patients still receiving stavudine.
我们评估了按照世界卫生组织2010年政策在撒哈拉以南非洲地区一线抗逆转录病毒治疗(ART)中逐步淘汰司他夫定与单药替代(SDS,即在一线ART中替换核苷类逆转录酶抑制剂)之间的关系。
前瞻性队列分析(国际评估艾滋病多区域流行病学数据库),纳入2005年1月至2012年12月期间开始接受ART治疗的至少16岁、未接受过ART的HIV感染患者。2010年4月之前(赞比亚为2007年7月),国家指南要求患者开始使用基于司他夫定或齐多夫定的治疗方案,而此后替诺福韦或齐多夫定在一线ART中取代了司他夫定。
我们评估了2004 - 2014年各日历年司他夫定的使用频率和单药替代情况。采用竞争风险回归分析来评估在接受ART治疗的前24个月中核苷类逆转录酶抑制剂的使用与单药替代之间的关联。
在接受ART治疗的前24个月中,377656例患者中共发生了33441例(8.9%;95%置信区间8.7 - 8.9%)单药替代,其中近40%发生在使用司他夫定的患者中。单药替代的减少与司他夫定的逐步淘汰相对应。竞争风险回归模型显示,与使用司他夫定的患者相比,使用替诺福韦的患者需要进行单药替代的可能性降低了20% - 95%,而与司他夫定相比,使用齐多夫定的患者单药替代风险降低了75% - 85%。
在我们的研究中,治疗前24个月单药替代的减少似乎与一线ART中用齐多夫定或替诺福韦逐步淘汰司他夫定有关。有必要进一步努力降低替诺福韦和齐多夫定在这种情况下的使用成本,以替代所有仍在使用司他夫定的患者。