TB Surrogate Markers for Assessing Reponse to Treatment (TB SMART Study)

用于评估治疗反应的结核病替代标志物（结核病 SMART 研究）

• 批准号: 9210047
• 负责人: PAYAM NAHID
• 金额: $ 114.24万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-02-12 至 2020-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9210047
• 关键词: Algorithms; Bioinformatics; Biological Assay; Biological Markers; Blood; Catalogs; Cells; Centers for Disease Control and Prevention (U.S.); Child; Classification; Clinical; Clinical Data; Clinical Trials; Coughing; Culture Media; Data; Data Set; Databases; Detection; Development; Diagnostic; Diagnostic radiologic examination; Disease; Dose; Drug Kinetics; Drug resistance; Drug toxicity; Enrollment; Extreme drug resistant tuberculosis; Failure; Funding; Goals; Gold; Growth; HIV; HIV/TB; Human; Immunoassay; Intention; Lead; Link; Liquid substance; Logistics; Measurement; Measures; Membrane; Microbiology; Monitor; Moxifloxacin; Mycobacterium tuberculosis; National Institute of Allergy and Infectious Disease; New Agents; Outcome; Participant; Patient Noncompliance; Patients; Performance; Pharmaceutical Preparations; Pharmacodynamics; Phase; Phase II Clinical Trials; Phase II/III Trial; Phase III Clinical Trials; Probability; Proteomics; Pulmonary Tuberculosis; Randomized; Randomized Clinical Trials; Reagent; Recording of previous events; Recovery; Regimen; Relapse; Sample Size; Sampling; Scientist; Serum; Signal Transduction; Specimen; Speed; Sputum; Statistical Data Interpretation; Surrogate Markers; Testing; Time; Treatment Failure; Treatment Protocols; Tuberculosis; Validation; Vesicle; arm; bactericide; base; biomarker discovery; biomarker identification; biomarker panel; blood-based biomarker; clinical development; cost; design; drug development; drug efficacy; efficacy testing; exosome; extensive drug resistance; follow-up; improved; industry partner; liquid chromatography mass spectrometry; macromolecule; next generation; novel; novel therapeutics; outcome prediction; pathogen; programs; prospective; prototype; public health relevance; repository; resistant strain; response; rifapentine; specific biomarkers; success; tool; treatment response; treatment trial; tuberculosis drugs; tuberculosis treatment; validation studies

DESCRIPTION (provided by applicant): The current recommended 6-month treatment regimen for active tuberculosis (TB) is more than 40 years old and suffers from issues with drug toxicity and high rates of patient non-adherence, which combined have contributed to the emergence of drug resistant strains. For the first time in decades, the TB drug development pipeline is filled with several promising new agents that will soon be ready for phase 2 and phase 3 trials. However, testing the efficacy of these agents in clinical trials is a significant challenge because the conventional sputum-based, growth-based, microbiologic trial endpoints have notable technical and logistical weaknesses. For this proposal, entitled TB Surrogate Markers for Assessing Response to Treatment (TB SMART Study), our objective is to develop a blood-based, quantitative, host and pathogen-specific biomarker assay using a proven, high sensitivity, multiplexed electrochemiluminescence (ECL) platform that can, in combination with clinical data, supplant 2-month sputum culture, the current dichotomous Phase 2 trial endpoint. A non-sputum, non-growth based biomarker assay applied early in the course of a trial that could replace microbiologic intermediate endpoints, while retaining or improving upon their ability to predict outcomes, could transform the pace and scope of TB drug development, and of global TB control. It may additionally have utility for monitoring treatment of paucibacillary disease as is often seen in children, extra-pulmonary TB, and HIV/TB. To achieve this goal, we have assembled an investigative team of academics with expertise in TB drug development; industry partners with expertise in both unbiased and directed approaches to biomarker discovery; exosome scientists; and statisticians with expertise in bioinformatic approaches to prediction and surrogate marker identification. We will take advantage of specimens linked to clinical, radiographic, microbiologic, and PK/PD data from well-characterized patients with culture-confirmed pulmonary TB enrolled in four studies: three CDC-funded, TB Trials Consortium randomized, clinical trials, and one FDA-funded repository linked to Phase 3 TB trials. We will use available clinical trial data and sample sets to: 1) Identify blood-based, host and TB-specific biomarkers of treatment response using unbiased, targeted and exosome-enriched approaches 2) develop and qualify multi-parameter classifiers for predicting recognized microbiologic measures of bactericidal and sterilizing activity, using the host and pathogen biomarkers identified, and 3) develop, qualify and conduct validation studies of a finalist biomarker panel built on a multiplexed ECL platform. Upon completion of comprehensive qualification and validation studies proposed, we will be ready to release the multiplexed, ECL biomarker panel assay as "Qualified Kits" to be used and evaluated in prospective Phase 2 and 3 trials.

描述（由申请人提供）：目前推荐的针对活动性结核病（TB）的6个月治疗方案已有40多年的历史，并且存在药物毒性和患者不依从性高的问题，这些问题共同导致了耐药菌株的出现。几十年来，结核病药物开发管道第一次充满了几种有希望的新药，它们将很快准备好进行2期和3期试验。然而，在临床试验中测试这些药物的疗效是一项重大挑战，因为传统的基于痰液、基于生长、微生物学的试验终点具有明显的技术和后勤弱点。在这个名为TB SMART研究的项目中，我们的目标是开发一种基于血液的、定量的、宿主和病原体特异性的生物标志物检测方法，该方法使用经过验证的、高灵敏度的、多路电化学发光（ECL）平台，结合临床数据，取代2个月的痰培养，即目前的2期试验终点。在试验早期应用一种非痰液、非生长为基础的生物标志物测定方法，可以取代微生物中间终点，同时保留或改进其预测结果的能力，从而改变结核病药物开发和全球结核病控制的速度和范围。此外，它还可用于监测儿童、肺外结核和艾滋病毒/结核中常见的少杆菌病的治疗。为了实现这一目标，我们组建了一个由具有结核病药物开发专业知识的学者组成的调查小组；在生物标志物发现的无偏见和定向方法方面具有专业知识的行业合作伙伴；外来体科学家;以及在生物信息学方法预测和替代标记识别方面具有专业知识的统计学家。我们将利用与临床、放射学、微生物学和PK/PD数据相关的标本，这些数据来自于四项研究中纳入的具有良好特征的培养确诊肺结核患者：三项由cdc资助的结核病试验联盟随机临床试验，以及一项由fda资助的与三期结核病试验相关的存储库。我们将使用现有的临床试验数据和样本集来：1)识别基于血液的宿主

项目成果

Diagnostic accuracy of 3 urine lipoarabinomannan tuberculosis assays in HIV-negative outpatients.

• DOI: 10.1172/jci140461
• 发表时间: 2020-11-02
• 期刊: The Journal of clinical investigation
• 作者: Broger T;Nicol MP;Sigal GB;Gotuzzo E;Zimmer AJ;Surtie S;Caceres-Nakiche T;Mantsoki A;Reipold EI;Székely R;Tsionsky M;van Heerden J;Plisova T;Chikamatsu K;Lowary TL;Pinter A;Mitarai S;Moreau E;Schumacher SG;Denkinger CM
• 通讯作者: Denkinger CM

Aptamer-based proteomic signature of intensive phase treatment response in pulmonary tuberculosis.

• DOI: 10.1016/j.tube.2014.01.006
• 发表时间: 2014-05
• 期刊: Tuberculosis (Edinburgh, Scotland)
• 作者: Nahid P;Bliven-Sizemore E;Jarlsberg LG;De Groote MA;Johnson JL;Muzanyi G;Engle M;Weiner M;Janjic N;Sterling DG;Ochsner UA
• 通讯作者: Ochsner UA

Biomarkers of Tuberculosis Severity and Treatment Effect: A Directed Screen of 70 Host Markers in a Randomized Clinical Trial.

• DOI: 10.1016/j.ebiom.2017.10.018
• 发表时间: 2017-11
• 期刊: EBioMedicine
• 影响因子: 11.1
• 作者: Sigal GB;Segal MR;Mathew A;Jarlsberg L;Wang M;Barbero S;Small N;Haynesworth K;Davis JL;Weiner M;Whitworth WC;Jacobs J;Schorey J;Lewinsohn DM;Nahid P
• 通讯作者: Nahid P

Clinical and bacteriological characteristics associated with clustering of multidrug-resistant tuberculosis.

• DOI: 10.5588/ijtld.16.0510
• 发表时间: 2017-07-01
• 期刊: The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease
• 作者: Feng JY;Jarlsberg LG;Salcedo K;Rose J;Janes M;Lin SG;Osmond DH;Jost KC;Soehnlen MK;Flood J;Graviss EA;Desmond E;Moonan PK;Nahid P;Hopewell PC;Kato-Maeda M
• 通讯作者: Kato-Maeda M

Second generation multiple reaction monitoring assays for enhanced detection of ultra-low abundance Mycobacterium tuberculosis peptides in human serum.

• DOI: 10.1186/s12014-017-9156-y
• 发表时间: 2017
• 期刊: Clinical proteomics
• 影响因子: 3.8
• 作者: Mehaffy C;Dobos KM;Nahid P;Kruh-Garcia NA
• 通讯作者: Kruh-Garcia NA