Ruth Moro M.D., M.P.H. Medical Epidemiologist. CDC, Division of Tuberculosis Elimination Clinical Research Branch Tuberculosis Trials Consortium

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Factors Associated with Non-completion of Latent Tuberculosis Infection (LTBI) Treatment: Reasons other than Adverse Events (AE) The TB Trials Consortium PREVENT TB Study 26 Ruth Moro M.D., M.P.H. Medical Epidemiologist CDC, Division of Tuberculosis Elimination Clinical Research Branch Tuberculosis Trials Consortium IUATLD, NAR, Boston, MA March 1, 2014 National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention Division of Tuberculosis Elimination

Background LTBI prophylactic treatment plays an important role in the US strategy for tuberculosis (TB) elimination. Treatment completion is a challenge since LTBI is asymptomatic and often not perceived as a real threat. Low completion rate of LTBI treatment compromises effectiveness and lowers protection against TB. Non-completion rate for 9INH has been reported as high as 53% by a study in 68 clinics in the US and Canada (Horsburgh et al). PREVENT TB (NEJM 2011) was a randomized open-label trial of 3 months onceweekly rifapentine (900 mg) plus isoniazid (900 mg) (3HP-(DOT)) versus 9 months daily isoniazid (300 mg, 9H-(SAT)). Overall rates of treatment non-completion were: 3HP 18 % 9H 31 %

Objectives To identify factors, other than AE, associated with non-completion of study 26 LTBI treatment, categorized by regimen. To identify potential predictors for non-completion of assigned treatment. Methods Participants enrolled, June 2001 - February 2008 (n= 8053) Participant sites: 27 clinics in USA, Canada, Brazil, and Spain a) 3HP: Directly Observed every week with monthly evaluation visits b) 9H: Self-administered daily with monthly evaluation visits Non-completion of treatment definition by regimen: a) 3HP: Failure to complete at least 11 of 12 doses in 10-16 weeks b) 9H: Failure to complete at least 240 of 270 doses in 35-52 weeks Missed early clinic visit: a) 3HP: Missing any of the first 3 of the 12 weekly DOTs b) 9H: Missing any of the first 3 of the 9 monthly visits

PREVENT TB Study Participants Included in the Analysis of Reasons for Non-completion of LTBI Treatment Total participants enrolled NEJM (n=8053)* **Study 26 ineligibles n=322 Included in the analysis n=6648 3HP=3430 9H=3218 Discontinuation due to an AE n=337 (9H=3.6% - 3HP=4.7%) Persons < 18 years of age n=632 Pregnancies n=114 Non-completion of treatment in 3HP 459/3430 = 13 % Non-completion of treatment in 9H 907/3218 = 28 % *Reported in the 2011 NEJM publication **Source case resistant to INH/RIF (50%), source case culture negative (31%), other (19%). This analysis considers adults age 18 or older.

Reasons for Non-completion of LTBI treatment, Other than AE (n=6648) 3HP (n=3430) 9H (n=3218) Frequency (n=459) %(3430) Frequency (n=907) %(3218) Lost for more than 3 months 58 1.7 280 8.7 Patient refused therapy 210 6.1 212 6.6 Non-compliant with schedule 60 1.7 121 3.8 Patient withdrew consent 52 1.5 64 2 Rx canceled by physician 17 0.5 47 1.5 *Other: 62 1.9 183 5.7 *3HP other: Moved out of state or to another country (13), incarcerated (10), unknown (39). *9H other: Moved out of state or to another country (36), incarcerated (15), error in dosages (7), schedule and legal issues (3), unknown (122).

Univariate Analysis of Factors Associated with Non-completion of LTBI Treatment - The PREVENT TB Study (n=6648) (1 of 2) OR 95% CI p-value Regimen (9H vs 3HP) 2.5 2.24, 2.88 <0.001 Age (median=37) (ref > 37) 1.1 0.97, 1.23 0.132 Sex (ref = female) 1.1 0.98, 1.24 0.118 Race (ref=white) African American Asian Other* 1.1 0.7 0.8 0.95, 1.26 0.61, 0.91 0.65, 0.95 0.236 0.004 0.012 HIV status (ref=hiv-non infected) Unknown Infected 0.8 0.9 0.73, 0.93 0.66, 1.33 0.002 0.725 Country of origin (ref=born in US) 0.8 0.67, 0.86 <0.001 Education (ref > college) < 8 grade 8 grade some college 1.1 1.4 0.92, 1.39 1.14, 1.61 0.245 0.001 > 1 month incarceration (ref=no) 2.0 1.59, 2.48 <0.001 *American Indian and others in US/non-US

Univariate Analysis of Factors Associated with Non-completion of LTBI Treatment - The PREVENT TB Study (n=6648) (2 of 2) OR 95% CI p-value Missed early clinic visit (ref=no) 6.5 5.64, 7.42 <0.001 Any unscheduled clinic visit (ref=no) 2.0 1.71, 2.24 <0.001 Homeless (ref=no)* 1.6 1.30, 1.97 <0.001 Injecting drug use ever (IDU) (ref=no) 1.6 1.20, 2.07 0.001 Cirrhosis (ref=no)** 1.5 1.12, 1.96 0.006 Current smoker (ref=no) 1.5 1.32, 1.69 <0.001 Unemployment > 1 year (ref=no) 1.4 1.17, 1.65 <0.001 Alcohol (ref=no) Use (only 1 yes to CAGE) Abuse (> 2 yes to CAGE) 1.3 2.0 1.15, 1.48 1.63, 2.50 <0.001 <0.001 Need of interpreter (ref=no) 0.9 0.74, 0.98 0.028 *Homeless or living in shelter > 6 months. **Medical history reported by patient.

Multivariate Analysis Final Model - Reasons for Non-completion of LTBI Treatment - The PREVENT TB study (n=6648) (1 of 2) OR 95% CI p-value Regimen (9H vs. 3HP) 2.1 1.5, 2.9 <0.001 Education (ref > college) < 8 grade 8 grade some college 1.1 1.3 1.05, 1.76 1.1, 1.63 0.020 0.004 > 1 month incarceration (ref=no) 1.5 1.11, 1.99 0.008 Alcohol (ref=no) Use (only 1 yes to CAGE) Abuse (> 2 yes to CAGE) 1.1 1.7 0.97, 1.31 1.3, 2.25 0.112 <0.001 Site (ref=20) <0.001 Current smoker x regimen 3HP 9H 0.98 1.4 0.76, 1.27 1.11, 1.63 0.049 Age x regimen 3HP (age<37) 9H (age<37) 0.9 1.3 0.76, 1.19 1.13, 1.59 0.016 Country of origin x regimen 3HP (US) 9H (US) 0.7 1.3 0.6, 0.98 1.1, 1.6 <0.001

Multivariate Analysis Final Model - Reasons for Non-completion of LTBI Treatment - The PREVENT TB study (n=6648) (2 of 2) OR 95% CI p-value Missed early clinic visit x regimen 3HP 9H 8.5 4.3 6.7, 10.66 3.57, 5.17 <0.001 IDU ever x regimen 3HP 9H 3.4 1.2 1.91, 6.03 0.73, 2.04 0.003 Any unscheduled clinic visit x regimen 3HP 9H 2.0 0.9 1.48, 2.74 0.73, 1.06 <0.001 Homeless x IDU ever Homeless No homeless 1.4 3.4 0.73, 2.65 1.9, 6.03 0.012 Need of interpreter x regimen 3HP 9H 0.7 1.0 0.49, 0.9 0.79, 1.28 0.024

Number of doses taken at the time participants stopped 3HP (%) (n=459) Failure to complete at least 11 of 12 doses in 10 to 16 weeks <10 doses: 367 >11doses in >16 weeks: 81(2.4%) >11doses in <10weeks: 7(0.2%) 13 doses in 10-16week: 4(0.1%)

Number of doses taken at the time participants stopped 9H (%) (n=907) Failure to complete at least 240 of 270 doses in 35 to 52 weeks <240doses: 708 >240 doses in >52 weeks: 142 (4.4%) >240 doses in <35 weeks: 0 >270 doses in 35-52 weeks: 57 (1.8%)

Limitations 3HP was an open-label clinical trial subject to bias 3HP was directly observed weekly, with more frequent interaction between providers and participants which probably improved compliance Variability among sites participating in the clinical trial not feasible to accurately evaluate individually

Summary Among 6648 adults, the factors associated with non-completion of treatment were 9H regimen, education less than a college degree, being incarcerated, alcohol consumption, or enrollment site In 9H arm: current smokers, participants younger than 37, born in the US, with history of injecting drugs, or missed at least 1 of the first 3 monthly visits were more likely not to complete treatment In the 3HP arm: participants with history of injecting drugs, missed at least 1 of the first 3 DOT, or had at least 1 unscheduled visit were more likely not to complete treatment Conclusions 3HP: less non-completion of treatment for reasons other than AEs 3HP and 9H share some common but also have some distinct predictors

Acknowledgments Andrey Borisov (CDC) Jussi Saukkonen (Boston University School of Medicine, US) Awal Khan (CDC) Nigel Scott (CDC) Nong Shang (CDC) Elsa Villarino (CDC) Timothy Sterling (Vanderbilt University School of Medicine, USA) Stefan Goldberg (CDC) Amy Kerrigan (Vanderbilt University School of Medicine, USA) Anne Efron (Johns Hopkins University, Baltimore MD, USA) Heilig Charles (CDC) Andrew Vernon (CDC) TBTC sites Sanofi (provided study drugs, supported sub-studies and some study staff) Disclaimer: Presentation reflects authors opinion and not official position of CDC