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Comment 258 www.thelancet.com/respiratory Vol 2 April 2014 The evolving role of advocacy in tuberculosis Published Online March 24, 2014 http://dx.doi.org/10.1016/ S2213-2600(14)70035-9 Tuberculosis advocacy has changed the disease from a silent epidemic to one with many voices that seek increased political will and investment in research. 1 Tuber- culosis advocacy has gained strength as a mechanism to improve research, increase access to new methods to fight tuberculosis, and involve communities in policy and programmatic decisions. 2,3 In the past few decades advocacy efforts for tuberculosis have contrasted starkly with those for HIV/AIDS. By making their protests visible and engaging intellectually with scientists and policy makers, HIV activists changed the course of AIDS research and global access to treatment. 4 However, few survivors of tuberculosis or other people affected by the disease have served as public voices for it, partly because of its curable nature, the vertical top-down orientation of efforts for tuberculosis control, the persistent stigma about tuberculosis worldwide, and the lack of funding to support community involvement in tuberculosis research and programmes. As a result, although the burden of tuberculosis remained large, and even grew in the wake of the HIV epidemic, communities were not empowered to engage in prevention and care for tuberculosis, much less to participate in research and development for new methods to fight the disease. 3 The advocacy movement for tuberculosis has grown as individuals and groups have developed their scientific literacy, becoming highly trained activists able to powerfully present community perspectives to scientists, policy makers, and industry. Public and non-profit sponsors of trials and other donors have begun to invest in advocacy. Guiding frameworks (eg, the Good Participatory Practice Guidelines for TB Drug Trials 5 ) are now available to enable effective engagement with communities and stakeholders at all stages of the research process. By encouraging early and frequent engagement, the guidelines can ensure communities’ needs are addressed in the research process. Affected communities now have many examples of how tuberculosis advocacy can affect decisions from trial design to programme implementation (figure). 1 Involvement of tuberculosis activists in the research process at the outset of trial design is one of the most direct methods to ensure that research addresses the priorities of affected communities. This involvement can include framing of the research question and revision of early drafts of protocols after a research question is developed. For example, the Global TB Community Advisory Board, an independent group of highly research-literate activists from global networks for HIV and tuberculosis, identified as an important concern for patients that bedaquiline (Janssen Therapeutics, Titusville, NJ, USA) and delamanid, the two newest drugs to fight drug-resistant tuberculosis, both cause QT prolongation. The advisory board called on the drugs’ sponsors to cooperate to establish if the drugs are safe to use together; the US National Institutes of Health is now arranging a drug–drug interaction study. After the design phase, advocates are uniquely positioned to affect the implementation of research, especially in ensuring effective communication between research sponsors and the communities hosting clinical trials. The Community Research Advisors Group, an independent advisory body, assists communication between investigators from the Tuberculosis Trials Consortium (TBTC) and local communities at all stages of research. Several members of the Community Research Advisors Group organise local community advisory boards to raise awareness of tuberculosis research in communities near TBTC sites. By empowering survivors of tuberculosis, affected family members, policy makers, religious leaders, and other community members to engage with study teams, these community advisory boards manifest the social value of tuberculosis research for communities. In addition to aiding recruitment, Before research begins Program implementation and policy change During research When research ends Framing of research questions Engagement of site communities Dissemination of results Uptake of evidence-based policies Access (early access, price, and registration) Support for recruitment, informed consent, and retention Practical implications of research Communication of priorities, concerns, and information Protocol review Ethics consultation Figure: Tuberculosis advocacy in action

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Page 1: The evolving role of advocacy in tuberculosis

Comment

258 www.thelancet.com/respiratory Vol 2 April 2014

The evolving role of advocacy in tuberculosisPublished Online

March 24, 2014http://dx.doi.org/10.1016/

S2213-2600(14)70035-9

Tuberculosis advocacy has changed the disease from a silent epidemic to one with many voices that seek increased political will and investment in research.1 Tuber-culosis advocacy has gained strength as a mechanism to improve research, increase access to new methods to fi ght tuberculosis, and involve com munities in policy and programmatic decisions.2,3

In the past few decades advocacy eff orts for tuberculosis have contrasted starkly with those for HIV/AIDS. By making their protests visible and engaging intellectually with scientists and policy makers, HIV activists changed the course of AIDS research and global access to treatment.4 However, few survivors of tuberculosis or other people aff ected by the disease have served as public voices for it, partly because of its curable nature, the vertical top-down orientation of eff orts for tuberculosis control, the persistent stigma about tuberculosis worldwide, and the lack of funding to support community involvement in tuberculosis research and programmes. As a result, although the burden of tuberculosis remained large, and even grew in the wake of the HIV epidemic, communities were not empowered to engage in prevention and care for tuberculosis, much less to participate in research and development for new methods to fi ght the disease.3

The advocacy movement for tuberculosis has grown as individuals and groups have developed their scientifi c literacy, becoming highly trained activists able to powerfully present community perspectives to scientists, policy makers, and industry. Public and non-profi t

sponsors of trials and other donors have begun to invest in advocacy. Guiding frameworks (eg, the Good Participatory Practice Guidelines for TB Drug Trials5) are now available to enable eff ective engagement with communities and stakeholders at all stages of the research process. By encouraging early and frequent engagement, the guidelines can ensure communities’ needs are addressed in the research process. Aff ected communities now have many examples of how tuberculosis advocacy can aff ect decisions from trial design to programme implementation (fi gure).1

Involvement of tuberculosis activists in the research process at the outset of trial design is one of the most direct methods to ensure that research addresses the priorities of aff ected communities. This involvement can include framing of the research question and revision of early drafts of protocols after a research question is developed. For example, the Global TB Community Advisory Board, an independent group of highly research-literate activists from global networks for HIV and tuberculosis, identifi ed as an important concern for patients that bedaquiline (Janssen Therapeutics, Titusville, NJ, USA) and delamanid, the two newest drugs to fi ght drug-resistant tuberculosis, both cause QT prolongation. The advisory board called on the drugs’ sponsors to cooperate to establish if the drugs are safe to use together; the US National Institutes of Health is now arranging a drug–drug interaction study.

After the design phase, advocates are uniquely positioned to aff ect the implementation of research, especially in ensuring eff ective communication between research sponsors and the communities hosting clinical trials. The Community Research Advisors Group, an independent advisory body, assists communication between investigators from the Tuberculosis Trials Consortium (TBTC) and local communities at all stages of research. Several members of the Community Research Advisors Group organise local community advisory boards to raise awareness of tuberculosis research in communities near TBTC sites. By empowering survivors of tuberculosis, aff ected family members, policy makers, religious leaders, and other community members to engage with study teams, these community advisory boards manifest the social value of tuberculosis research for communities. In addition to aiding recruitment,

Before research begins

Program implementationand policy change

During research

When research ends

Framing of researchquestions

Engagement of sitecommunities

Dissemination of results

Uptake of evidence-basedpolicies

Access (early access,price, and registration)

Support for recruitment,informed consent,and retention

Practical implicationsof research

Communication ofpriorities, concerns,and information

Protocol review

Ethics consultation

Figure: Tuberculosis advocacy in action

Page 2: The evolving role of advocacy in tuberculosis

Comment

www.thelancet.com/respiratory Vol 2 April 2014 259

enrolment, and retention of participants in TBTC studies, community advisory boards could help communities to accept tuberculosis research as a long-lasting partnership extending beyond the duration of any individual trial.

When studies conclude and investigators publish results, tuberculosis activists can play a crucial part to ensure that participants receive and understand fi ndings, and that research developments translate into practical changes for aff ected populations. For example, fi ndings from publicly funded research showed that rifapentine could reduce treatment lengths and provide intermittent dosing for patients with tuberculosis.6,7 After these trials, the advocacy organisation Treatment Action Group and partners from the public sector, academia, and other advocacy groups identifi ed price as an obstacle to imple-mentation of rifapentine-based treatment in the USA.8 While engaging with the drug’s sponsor, the Treatment Action Group and partners administered a survey among US tuberculosis controllers in which price was the most cited barrier to use of rifapentine. The Treatment Action Group dis cussed this evidence with the drug company Sanofi US, which eventually voluntarily reduced the drug’s price by 57%.

Tuberculosis advocates also play a prominent role in shaping of policy and control programmes. Health-care workers—a previously underused resource, who face a three times higher risk of contracting tuberculosis and up to fi ve times higher risk of contracting drug-resistant tuberculosis than do the general population9,10—are also highly empowered, because of their access to information and training and their ability to aff ect policy and implementation of health care. A growing community of health-care workers and students who are tuberculosis survivors, collectively known as TB Proof, are using dual perspectives and professional networks as platforms to call for improved tuberculosis prevention and accelerated access to urgently needed new regimens and vaccines.

Tuberculosis advocacy has recently increased at a rapid pace and achieved successful outcomes; this trend must continue to reach global targets for tuberculosis elimination.11 At present, only a few trial sponsors engage communities in research; concrete and systemic engagement with communities is therefore needed from all tuberculosis scientists at each step of the research and development process, particularly in the pretrial and post-trial phases. Mechanisms include dedicated funding for community engagement,

establishment of networks for activists to communicate with each other at national and international levels, and a commitment by all stakeholders to make tuberculosis advocacy an equal partner of processes for research, development, and policy planning. An environment in which tuberculosis survivors and advocates can aff ect research and ensure access to lifesaving technologies needs respect for the independence, autonomy, and professionalism of acti vists, and the end of persistent stigma about the disease.

*Andrea DeLuca, Erica Lessem, Donna Wegener, Laia Ruiz Mingote, Mike Frick, Dalene Von DelftCenter for Tuberculosis Research, Johns Hopkins University, Baltimore, MD 21231, USA (AD); Treatment Action Group, New York, NY, USA (EL, MF); National Tuberculosis Controllers Association, Smyrna, GA, USA (DW); Planeta Salud, Barcelona, Spain (LRM); and TB Proof, Somerset West, South Africa (DVD)[email protected]

We thank Alicia Chou for providing information about the Good Participatory Practice Guidelines for TB Drug Trials and also for her feedback, and Marco Schito for his feedback. LRM is cochair of the Community Research Advisors Group (CRAG). The CRAG receives limited funds from the Centers for Disease Control and Prevention to support its work with the Tuberculosis Trials Consortium. LRM receives no compensation for her involvement with CRAG, and all CRAG activities are done on a volunteer basis. MF is employed by the Treatment Action Group and provides technical and administrative support to the CRAG; the Treatment Action Group has several funding sources. All other authors declare that they have no competing interests. No funding from the Centers for Disease Control and Prevention or other public funding was used for the creation of this Comment. The opinions expressed herein are those of the authors.

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11 World Health Assembly Executive Board. Global strategy and targets for tuberculosis prevention, care and control after 2015. Geneva: World Health Organization, 2014.