Can TB Be Eliminated?

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Transcription:

Can TB Be Eliminated? Richard E. Chaisson, MD Center for AIDS Research Center for TB Research Johns Hopkins University

The Global Burden of TB -2015 All forms of TB HIV-associated TB MDR TB / RR TB Estimated number of cases 10.4 million (8.7 12.2 million) (IR=142/100,000) 1.2 million (11%) (1.0 1.3 million) 580,000 (520,000-640,000) Estimated number of deaths 1.8 million* (1.5-2.1) *1.4 million among HIV negative 390,000 (22%) (320,000-460,000) 250,000 (160,000 340,000) WHO Global Tuberculosis Report 2016

WHO Global Tuberculosis Report 2016

TB is now leading infectious cause of death WHO Global Tuberculosis Report 2016

Vision, goal, targets, milestones Vision: A world free of TB Zero TB deaths, Zero TB disease, and Zero TB suffering Goal: End the Global TB epidemic

Eradication, elimination or control? Eradication complete absence of the disease from the planet. Elimination ending the disease as a public health problem. Defined as TB incidence of <1 per million and TB deaths <1 per 10 million Control making it a much smaller problem than it currently is.

Tools to Control of Tuberculosis Why hasn t TB already been eliminated? Global failure to apply biomedical tools effectively Weaknesses in health systems Lack of political will and commitment Inadequacies of most widely used tools Smear detection of cases ~50% Adherence to regimens is poor and MDR TB regimens are toxic and weak BCG vaccine does not prevent adult TB Changing epidemiological situation HIV epidemic MDR Migration Global policies that lack understanding of best epidemiologic approaches

Latent TB (Global ~ 2 billion) Reduce and treat individual drivers (HIV) Case finding and treatment of active TB Active TB (Global ~6-7 million/year) Uninfected/Susceptible (5 billion) Vaccination TB Preventive Rx Primary TB (~2-3 million/year)

Modeled approaches to reaching TB elimination Dye, et al., Ann Rev Publ Health 2013

A Platform for Controlling Global Tuberculosis FIND the TB that is there Passive case detection is not sufficient Improved diagnostic technologies very important Better case finding strategies essential TREAT the TB that is found Improved treatment outcomes essential M/XDR is abysmal New drugs and treatment strategies urgently needed PREVENT the TB that hasn t occurred yet Preventive therapy essential for high risk populations Infection (transmission) control critical Control susceptibility (antiretrovirals, diabetes control) New vaccine

TB Case Detection: Missed Cases Drive Transmission and Mortality WHO Global Tuberculosis Report 2013

Adults dying at home, no specific diagnosis (18% excluded, known to have TB) Consent from family Bilateral axillary Tru-Cut biopsy Modified bronchoalveolar lavage

Tuberculosis found at limited autopsy in adults dying at home from natural causes Omar et al., Int J Tuberc Lung Dis 2015,19:1320-5 Post-Mortem Diagnosis N=85 (%) TB on 1 lab test 27 (32) TB on 2 lab tests 18 (21) Biopsy with TB (N=20) Histology 14/20 (70) AFB positive (ZN) 7/20 (35) Xpert 17/20 (63) MGIT 18/29 (62.1) BAL with TB (N=22) AFB+ (Auramine) 9/22 (41) Xpert 20/22 (91) MGIT 19/29 (86)

New Tools for Diagnosing TB Xpert MTB/RIF Ultra Omni Xpert Platform Abbott BD Max New tools are exciting and attractive, but do they make a difference in incidence of disease or death?

Southern Africa Zambia Western Cape 0 1 5 3 0 K m Western Cape Zambia 0 2 40 0 0 0 K

ZAMSTAR Interventions: Enhanced Case finding vs. Household Contact Screening Enhanced case finding (ECF) Community Mobilization and sputum collection School intervention Open Access at the clinic Household intervention (HH) Visit all households of new TB patients Offer TB screening, HIV testing and referral to appropriate care to entire household

Impact of Household Contact Evaluations for New TB Patients or Community Active TB Case (ECF) Finding in High Burden Areas 0.45 0.82 18% 55% Household Evaluations: Impact on TB prevalence Household Evaluations: impact on transmission in children 1.09 ECF impact on TB prevalence 1.36 ECF impact on transmission in children 0.13 0.25 0.50 1.00 2.00 4.00 8.00 16.00 Risk ratios (for prevalence) and Rate ratios (for transmission) H. Ayles, et al., Lancet, 2013

Impact of Improving Case Finding and Treatment on Tuberculosis Control: A Mathematical Model Annual Decline in TB Incidence (%) 15 10 5 0 Case Detection Rate: 20% 40% 60% 70% 80% 0 2 4 6 8 10 Years After Stabilization of Case Detection Rate Effect of case-finding plateaus eventually Dowdy and Chaisson, Bull WHO 2009, 87:296 304

PERÚ: TASA DE MORBILIDAD E INCIDENCIA DE TUBERCULOSIS. 1990 2014* 300.0 250.0 TASA POR 100 000 HABITANTES 200.0 150.0 100.0 50.0 0.0 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 * MORBILIDAD 198. 202. 256. 248. 227. 208. 198. 193. 186. 165. 155. 146. 140. 123. 124. 129. 129. 125. 120. 118. 109. 109. 105. 101. 100. INCID TBC 183. 192. 243. 233. 215. 196. 161. 158. 156. 141. 133. 126. 121. 107. 107. 109. 109. 106. 103. 102. 95.7 97.4 93.0 90.3 87.5 INCID TBP FP 116. 109. 148. 161. 150. 139. 111. 112. 111. 97.1 87.9 83.1 77.4 68.8 66.4 67.1 67.9 64.5 63.9 61.9 58.3 59.7 58.6 55.3 54.7 * Información preliminar Fuente: ESNPCT /DGSP /MINSA /PERU Fecha de Elaboración.: 17-MAR-2015

CDC, 2016

Cavalcante et al., Int J TB Lung Dis 2010:14:203-9 Contact evaluation: combining TB case finding and TB preventive therapy: DOTS Ampliado (Enhanced DOTS) Cluster-randomized trial in 8 neighborhoods in central Rio de Janeiro comparing standard DOTS to DOTS Ampliado DOTS Ampliado: Identification of all household contacts (household visits) Evaluation with PPD, x-ray and clinical exam 4% of contacts had active TB 72% of contacts had latent TB ~70% of contacts treated with preventive therapy

Community-Randomized Trial of Household Contact Evaulation and Preventive Therapy (DOTS-A) vs DOTS in Rio de Janeiro TB Incidence/100,000 450 400 350 300 250 200 150 100 50 0 1999 2000 2001 2002 2003 2004 Year 15% difference p=0.04, 1999 vs. 2004 DOTS DOTS-A Cavalcante et al., Int J TB Lung Dis 2010:14:203-9

Preventive Interventions in TB Prevent Infection Reduce Chemoprophylaxis Susceptibility TB and HIV vaccines obvious additional strategies, but not currently available

Prevalence of latent tuberculosis infection in rural China Tuberculin Skin Test >10 mm Quantiferon test positive Tuberculin Skin Test >10 mm Quantiferon test positive Gao, et al. Lancet Infect Dis 2015:15;310-9

Preventive Interventions in TB: Impact of ART on TB Incidence in HIV+ People Reduce Susceptibility A.B Suthar, et al. PLoS Medicine, 2012

TB-HIV in Rio (THRio): Improving the uptake of TB screening and INH preventive therapy (IPT) in people receiving care of HIV infection in Rio de Janeiro Control Intervention 1 2 3 4 5 30 36 42 Month

Intervention Training for 2 clinics every other month Implementation of TB screening and TST policy for all HIV-infected patients TST to be done for all eligible clinic patients No prior TB history No prior IPT No prior +TST IPT x 6 months for all TST+ without active TB and all contacts of active TB cases 28

Clinic-level Outcome Cases Crude HR (95% CI) p-value TB 475 0.87 (0.69-1.10) 0.24 TB or Death 1313 0.76 (0.66-0.87) <0.001 Adjusted HR* (95% CI) 0.73 (0.54-0.99) 0.69 (0.57-0.83) p-value 0.04 <0.001 *Adjusted for age, sex, ART and CD4 count at enrollment Lancet Infect Dis. 2013;10:852-8

Long term efficacy of IPT in HIV-infected persons in a medium TB burden setting: Rio de Janeiro Cumulative probability of tuberculosis 0.00 0.05 0.10 0.15 0.20 0.25 Did not start IPT Started IPT Number at risk (events) Did not start IPT Started IPT 1 mo 1 yr 2 yr 3 yr 4 yr 5 yr 6 yr 7 yr Years since PPD+ 1222 (58) 400 (14) 318 (9) 241 (1) 168 (2) 123 (2) 84 (0) 62 732 (7) 1470 (12) 1506 (12) 1437 (2) 1149 (5) 790 (3) 414 (0) 189 Golub, et al. CID, 2015

TEMPRANO: Immediate vs Deferred ART Initiation and IPT Delivery for African Patients Not Eligible for ART Cumulative Probability of Death or Severe HIV-Related Illness (%) 25 20 15 10 5 30-Mo Probability, % Deferred ART 14.1 Deferred ART + IPT 8.8 Immediate ART 7.4 Immediate ART + IPT 5.7 0 0 6 12 18 24 30 Mos From Randomization TEMPRANO ANRS 12136 Study Group. N Engl J Med. 2015

Poor Global Uptake of IPT for People with HIV WHO. Global TB Report, 2016

The Cascade of Care for Latent TB 31% start PT 18.8% complete PT Alsdurf et al., Lancet ID, 2016

TEKO Study Interferon Gamma Release Assay Blood Test vs Tuberculin Skin Test to Screen HIV+ People for TB IGRA Clinics Eligible 1214 (76%) Standard-of-Care (TST) Eligible 990 (78%) Enrolled n = 1169 (96%) Enrolled n = 933 (94%) Valid Result Obtained 903 (76%) Valid Result Obtained 83 (6%) Martinson and Golub, IUATLD 2016

Cluster-Randomized Trial of Nurse-initiated IPT based on symptom screening vs TST-based screening 16 Matlosana Sub-district Primary Care Clinics Restricted Randomization -Mean No. TB cases/month -Distance from Hospital Koombi fare Salazar-Austin, CROI 2017 8 clinics: TSTbased Screening Symptombased Screening Endpoint: Proportion of child contacts started on IPT

Screening and provision of INH preventive therapy to child contacts in Matlosana Health District, October 2015 March 2016 Cascade of Child Contact Evaluation 1400 1200 1173 1000 821 800 600 400 200 408 202 185 Estimated INH Coverage for Child Household Contacts = 22% Salazar-Austin, CROI 2017 0 # TB Index Cases # EstimatedContacts < 5 yr # IdentifiedContacts < 5 # ScreenedContacts < 5 # Contacts Initiated Treatment

1 month of daily rifapentine/inh (HP) vs 9 months of daily INH ACTG A5279 Study Design: Multicenter, randomized, open-label, phase III clinical trial Study Population: 3000 HIV-infected participants >12 years old in 13 countries Stratification 1) CD4+ cell count at entry (<100, 100-250, and >250 cells/mm 3 ) 2) ART use at entry (Yes/No 50% on ART at entry) Duration: 3 years (156 weeks) after the last participant is enrolled R. Chaisson and S. Swindells, Co-Chairs

Target Populations for TB Control in Developed Countries Active case finding and preventive therapy Immigrants and refugees from high-burden countries Immunosuppressed patients HIV TNF and cytokine inhibitors Transplant and chemotherapy Injection drug users Prisoners Homeless Comorbidities: smoking, diabetes, end-stage renal disease

Understanding Local Drivers of TB Risk Factors in Patients with Culture-Confirmed Pulmonary TB in Baltimore Characteristic No. (Total = 139) % Foreign born 12 9% HIV Infection 31 24% IDU 28 20% Diabetes 18 14% Renal Failure 12 9% Recent Cancer 8 6% Steroid Use 7 6% Oursler et al., CID 2002;34:729-9

How to improve TB control globally Increase case finding Better diagnostic tests Active case finding, especially in household contacts Initiate treatment early and improve outcomes Reduce early losses to follow up Better regimens Prevent TB in high-risk populations Preventive therapy for those at increased risk Better regimens sterilizing regimens in high-burden settings Reduce susceptibility, e.g., ART

Can TB be eliminated? Probably not by 2035 or even 2050. Can TB be controlled? Yes, with investment in epidemiologically sound strategies and tools and greatly improved delivery.

JHU/PHRU Jonathan Golub Neil Martinson David Dowdy Larry Moulton Nicole Salazar-Austin Silvia Cohn Bonnie King Grace Link Barnes Anne Efron Susan Dorman Jenny Hoffmann Chris Hoffmann Acknowledgements ZAMSTAR Peter Godfrey-Faussett Helen Ayles Nulda Beyers Richard Hayes THRio Solange Cavalcante Betina Durovni Valeria Saraceni ACTG Sue Swindells TBTC Tim Sterling Elsa Villarino Marcus Conde Funders: Fogarty Int l Center NIDA NIAID/NIH CDC FDA Bill and Melinda Gates Foundation