Yuen Courtney M, Kurbatova Ekaterina V, Tupasi Thelma, Caoili Janice Campos, Van Der Walt Martie, Kvasnovsky Charlotte, Yagui Martin, Bayona Jaime, Contreras Carmen, Leimane Vaira, Ershova Julia, Via Laura E, Kim HeeJin, Akksilp Somsak, Kazennyy Boris Y, Volchenkov Grigory V, Jou Ruwen, Kliiman Kai, Demikhova Olga V, Vasilyeva Irina A, Dalton Tracy, Cegielski J Peter
Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Tropical Disease Foundation, Manila, Philippines.
PLoS Med. 2015 Dec 29;12(12):e1001932. doi: 10.1371/journal.pmed.1001932. eCollection 2015 Dec.
For treating multidrug-resistant tuberculosis (MDR TB), the World Health Organization (WHO) recommends a regimen of at least four second-line drugs that are likely to be effective as well as pyrazinamide. WHO guidelines indicate only marginal benefit for regimens based directly on drug susceptibility testing (DST) results. Recent evidence from isolated cohorts suggests that regimens containing more drugs may be beneficial, and that DST results are predictive of regimen effectiveness. The objective of our study was to gain insight into how regimen design affects treatment response by analyzing the association between time to sputum culture conversion and both the number of potentially effective drugs included in a regimen and the DST results of the drugs in the regimen.
We analyzed data from the Preserving Effective Tuberculosis Treatment Study (PETTS), a prospective observational study of 1,659 adults treated for MDR TB during 2005-2010 in nine countries: Estonia, Latvia, Peru, Philippines, Russian Federation, South Africa, South Korea, Thailand, and Taiwan. For all patients, monthly sputum samples were collected, and DST was performed on baseline isolates at the US Centers for Disease Control and Prevention. We included 1,137 patients in our analysis based on their having known baseline DST results for at least fluoroquinolones and second-line injectable drugs, and not having extensively drug-resistant TB. These patients were followed for a median of 20 mo (interquartile range 16-23 mo) after MDR TB treatment initiation. The primary outcome of interest was initial sputum culture conversion. We used Cox proportional hazards regression, stratifying by country to control for setting-associated confounders, and adjusting for the number of drugs to which patients' baseline isolates were resistant, baseline resistance pattern, previous treatment history, sputum smear result, and extent of disease on chest radiograph. In multivariable analysis, receiving an average of at least six potentially effective drugs (defined as drugs without a DST result indicating resistance) per day was associated with a 36% greater likelihood of sputum culture conversion than receiving an average of at least five but fewer than six potentially effective drugs per day (adjusted hazard ratio [aHR] 1.36, 95% CI 1.09-1.69). Inclusion of pyrazinamide (aHR 2.00, 95% CI 1.65-2.41) or more drugs to which baseline DST indicated susceptibility (aHR 1.65, 95% CI 1.48-1.84, per drug) in regimens was associated with greater increases in the likelihood of sputum culture conversion than including more drugs to which baseline DST indicated resistance (aHR 1.33, 95% CI 1.18-1.51, per drug). Including in the regimen more drugs for which DST was not performed was beneficial only if a minimum of three effective drugs was present in the regimen (aHR 1.39, 95% CI 1.09-1.76, per drug when three effective drugs present in regimen). The main limitation of this analysis is that it is based on observational data, not a randomized trial, and drug regimens varied across sites. However, PETTS was a uniquely large and rigorous observational study in terms of both the number of patients enrolled and the standardization of laboratory testing. Other limitations include the assumption of equivalent efficacy across drugs in a category, incomplete data on adherence, and the fact that the analysis considers only initial sputum culture conversion, not reversion or long-term relapse.
MDR TB regimens including more potentially effective drugs than the minimum of five currently recommended by WHO may encourage improved response to treatment in patients with MDR TB. Rapid access to high-quality DST results could facilitate the design of more effective individualized regimens. Randomized controlled trials are necessary to confirm whether individualized regimens with more than five drugs can indeed achieve better cure rates than current recommended regimens.
为治疗耐多药结核病(MDR-TB),世界卫生组织(WHO)推荐使用至少四种可能有效的二线药物以及吡嗪酰胺组成的治疗方案。WHO指南指出,直接基于药敏试验(DST)结果的治疗方案仅具有边际效益。来自孤立队列的最新证据表明,包含更多药物的治疗方案可能有益,并且DST结果可预测治疗方案的有效性。我们研究的目的是通过分析痰培养转阴时间与治疗方案中潜在有效药物数量以及方案中药物的DST结果之间的关联,深入了解治疗方案设计如何影响治疗反应。
我们分析了“保留有效结核病治疗研究”(PETTS)的数据,这是一项前瞻性观察性研究,在2005年至2010年期间对爱沙尼亚、拉脱维亚、秘鲁、菲律宾、俄罗斯联邦、南非、韩国、泰国和台湾九个国家的1659名接受MDR-TB治疗的成年人进行了研究。对于所有患者,每月收集痰样本,并在美国疾病控制与预防中心对基线分离株进行DST。我们纳入了1137名患者进行分析,这些患者至少有氟喹诺酮类和二线注射药物的已知基线DST结果,且没有广泛耐药结核病。这些患者在开始MDR-TB治疗后中位随访20个月(四分位间距16 - 23个月)。感兴趣的主要结局是初始痰培养转阴。我们使用Cox比例风险回归,按国家分层以控制与环境相关的混杂因素,并对患者基线分离株耐药的药物数量、基线耐药模式、既往治疗史、痰涂片结果和胸部X线片上的疾病范围进行调整。在多变量分析中,每天平均接受至少六种潜在有效药物(定义为DST结果未显示耐药的药物)与每天平均接受至少五种但少于六种潜在有效药物相比,痰培养转阴的可能性高36%(调整后风险比[aHR] 1.36,95% CI 1.09 - 1.69)。治疗方案中包含吡嗪酰胺(aHR 2.00,95% CI 1.65 - 2.41)或基线DST显示敏感的更多药物(每种药物aHR 1.65,95% CI 1.48 - 1.84)与痰培养转阴可能性的增加幅度大于包含基线DST显示耐药的更多药物(每种药物aHR 1.33,95% CI 1.18 - 1.51)相关。仅当治疗方案中至少有三种有效药物时,在治疗方案中纳入更多未进行DST的药物才有益(当治疗方案中有三种有效药物时,每种药物aHR 1.39,95% CI 1.09 - 1.76)。该分析的主要局限性在于它基于观察性数据而非随机试验,并且不同地点的药物治疗方案有所不同。然而,就纳入的患者数量和实验室检测的标准化而言,PETTS是一项独特的大型且严谨的观察性研究。其他局限性包括假设同一类药物的疗效等同、依从性数据不完整,以及该分析仅考虑初始痰培养转阴,而非复阳或长期复发。
与WHO目前推荐的至少五种药物的最低标准相比,包含更多潜在有效药物的MDR-TB治疗方案可能会促进MDR-TB患者对治疗的更好反应。快速获取高质量的DST结果有助于设计更有效的个体化治疗方案。需要进行随机对照试验以确认超过五种药物的个体化治疗方案是否确实能比当前推荐方案取得更好的治愈率。