TY - JOUR
T1 - Using biomarkers to predict TB treatment duration (Predict TB)
T2 - A prospective, randomized, noninferiority, treatment shortening clinical trial
AU - Predict TB Study Group
AU - Chen, Ray Y.
AU - Via, Laura E.
AU - Dodd, Lori E.
AU - Walzl, Gerhard
AU - Malherbe, Stephanus T.
AU - Loxton, André G.
AU - Dawson, Rodney
AU - Wilkinson, Robert J.
AU - Thienemann, Friedrich
AU - Tameris, Michele
AU - Hatherill, Mark
AU - Diacon, Andreas H.
AU - Liu, Xin
AU - Xing, Jin
AU - Jin, Xiaowei
AU - Ma, Zhenya
AU - Pan, Shouguo
AU - Zhang, Guolong
AU - Gao, Qian
AU - Jiang, Qi
AU - Zhu, Hong
AU - Liang, Lili
AU - Duan, Hongfei
AU - Song, Taeksun
AU - Alland, David
AU - Tartakovsky, Michael
AU - Rosenthal, Alex
AU - Whalen, Christopher
AU - Duvenhage, Michael
AU - Cai, Ying
AU - Goldfeder, Lisa C.
AU - Arora, Kriti
AU - Smith, Bronwyn
AU - Winter, Jill
AU - Barry, Clifton E.
AU - Lourens, Madeleine
AU - Patientia, Ramonde
AU - Mukasa, Sandra
AU - Goliath, Rene
AU - Omar-Davies, Nashreen
AU - Swanepoel, Loriane
AU - Morar, Tania
AU - Oelofse, Rachel
AU - Geldenhuys, Hennie
AU - Luabeya, Angelique
AU - Shenje, Justin
AU - Swarts, Anne
AU - Ockhuis, Rose
AU - Khomba, Gloria
AU - Mabwe, Simba
N1 - Funding Information:
Grant information: Bill and Melinda Gates Foundation [OPP1155128]; the European and Developing Countries Clinical Trials Partnership [96425], China Ministry of Science and Technology [2014DFA30340], National Natural Science Foundation of China, the Intramural Research Program of the NIAID, NIH, and the National Institutes of Health [1U01AI115619-01].
Funding Information:
Bill and Melinda Gates Foundation [OPP1155128]; the European and Developing Countries Clinical Trials Partnership [96425], China Ministry of Science and Technology [2014DFA30340], National Natural Science Foundation of China, the Intramural Research Program of the NIAID, NIH, and the National Institutes of Health [1U01AI115619-01].
Publisher Copyright:
© 2017 Chen RY et al.
PY - 2017
Y1 - 2017
N2 - Background: By the early 1980s, tuberculosis treatment was shortened from 24 to 6 months, maintaining relapse rates of 1-2%. Subsequent trials attempting shorter durations have failed, with 4-month arms consistently having relapse rates of 15-20%. One trial shortened treatment only among those without baseline cavity on chest x-ray and whose month 2 sputum culture converted to negative. The 4-month arm relapse rate decreased to 7% but was still significantly worse than the 6-month arm (1.6%, P<0.01). We hypothesize that PET/CT characteristics at baseline, PET/CT changes at one month, and markers of residual bacterial load will identify patients with tuberculosis who can be cured with 4 months (16 weeks) of standard treatment. Methods: This is a prospective, multicenter, randomized, phase 2b, noninferiority clinical trial of pulmonary tuberculosis participants. Those eligible start standard of care treatment. PET/CT scans are done at weeks 0, 4, and 16 or 24. Participants who do not meet early treatment completion criteria (baseline radiologic severity, radiologic response at one month, and GeneXpert-detectable bacilli at four months) are placed in Arm A (24 weeks of standard therapy). Those who meet the early treatment completion criteria are randomized at week 16 to continue treatment to week 24 (Arm B) or complete treatment at week 16 (Arm C). The primary endpoint compares the treatment success rate at 18 months between Arms B and C. Discussion: Multiple biomarkers have been assessed to predict TB treatment outcomes. This study uses PET/CT scans and GeneXpert (Xpert) cycle threshold to risk stratify participants. PET/CT scans are not applicable to global public health but could be used in clinical trials to stratify participants and possibly become a surrogate endpoint. If the Predict TB trial is successful, other immunological biomarkers or transcriptional signatures that correlate with treatment outcome may be identified.
AB - Background: By the early 1980s, tuberculosis treatment was shortened from 24 to 6 months, maintaining relapse rates of 1-2%. Subsequent trials attempting shorter durations have failed, with 4-month arms consistently having relapse rates of 15-20%. One trial shortened treatment only among those without baseline cavity on chest x-ray and whose month 2 sputum culture converted to negative. The 4-month arm relapse rate decreased to 7% but was still significantly worse than the 6-month arm (1.6%, P<0.01). We hypothesize that PET/CT characteristics at baseline, PET/CT changes at one month, and markers of residual bacterial load will identify patients with tuberculosis who can be cured with 4 months (16 weeks) of standard treatment. Methods: This is a prospective, multicenter, randomized, phase 2b, noninferiority clinical trial of pulmonary tuberculosis participants. Those eligible start standard of care treatment. PET/CT scans are done at weeks 0, 4, and 16 or 24. Participants who do not meet early treatment completion criteria (baseline radiologic severity, radiologic response at one month, and GeneXpert-detectable bacilli at four months) are placed in Arm A (24 weeks of standard therapy). Those who meet the early treatment completion criteria are randomized at week 16 to continue treatment to week 24 (Arm B) or complete treatment at week 16 (Arm C). The primary endpoint compares the treatment success rate at 18 months between Arms B and C. Discussion: Multiple biomarkers have been assessed to predict TB treatment outcomes. This study uses PET/CT scans and GeneXpert (Xpert) cycle threshold to risk stratify participants. PET/CT scans are not applicable to global public health but could be used in clinical trials to stratify participants and possibly become a surrogate endpoint. If the Predict TB trial is successful, other immunological biomarkers or transcriptional signatures that correlate with treatment outcome may be identified.
KW - Biomarkers
KW - Cycle threshold
KW - Drug sensitive
KW - GeneXpert
KW - MERM
KW - PET/CT
KW - Pulmonary tuberculosis
KW - Treatment shortening
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UR - http://www.scopus.com/inward/citedby.url?scp=85057752188&partnerID=8YFLogxK
U2 - 10.12688/gatesopenres.12750.1
DO - 10.12688/gatesopenres.12750.1
M3 - Article
AN - SCOPUS:85057752188
SN - 2572-4754
VL - 1
JO - Gates Open Research
JF - Gates Open Research
M1 - 9
ER -