This information collection is a core HTA, i.e. an extensive analysis
of one or more health technologies using all nine domains of the HTA Core Model.
The core HTA is intended to be used as an information base for local
(e.g. national or regional) HTAs.
Use of Intravenous immunoglobulins for Alzeheimer’s disease including Mild Cognitive Impairment
Immunoglobulins (IGG) compared to placebo, not doing anything or Usual supportive care in the treatment of Alzheimer’s disease in elderly AD is diagnosed mostly in people over 65 years of age, although there is an early-onset form that can occur much earlier. According to Wikipedia in 2006, there were 26.6 million sufferers worldwide.
(See detailed scope below)
HTA Core Model Application for Pharmaceuticals (2.0)
Tom Jefferson (Agenas - Italy), Marina Cerbo (Agenas - Italy), Nicola Vicari (Agenas - Italy)
Alessandra Lo Scalzo (Agenas), Anna-Theresa Renner (GOG), Antonio Migliore (Agenas), Ingrid Wilbacher (HVB), Luca Vignatelli (ASSR RER), Luciana Ballini (ASSR RER), Nadine Berndt (CEM), Nicola Vicari (Agenas), Plamen Dimitrov (NCPHA), Susanna Maltoni (ASSR RER), Ricardo Ramos (INFARMED), Tom Jefferson (Agenas)
Agenas - Agenzia nazionale per i servizi sanitari regionali
Jefferson T, Cerbo M, Vicari N [eds.]. Use of Intravenous immunoglobulins for Alzeheimer’s disease including Mild Cognitive Impairment [Core HTA], Agenas - Agenzia nazionale per i servizi sanitari regionali ; 2015. [cited 22 June 2018]. Available from: http://meka.thl.fi/ViewCover.aspx?id=267
Naturally occurring proteins produced by the body’s immune system to combat foreign antigens
Intended use of the technology
Treatment of Alzheimer’s disease
Target condition description
Alzheimer's disease (AD) or Alzheimer disease, is the most common form of dementia. There is no cure for the disease, which worsens as it progresses, and eventually leads to death.
Target population sex: Any.
Target population age: elderly. Target population group: Patients who have the target condition.
Target population description
AD is diagnosed mostly in people over 65 years of age, although there is an early-onset form that can occur much earlier. According to Wikipedia in 2006, there were 26.6 million sufferers worldwide.
placebo, not doing anything or Usual supportive care
There is no MA for IGGs for AD yet and there is no other intervention licensed for use in AD so the comparison would have to be against placebo or best supportive care
Description of aims of technology (TECH)
Regulatory status (CUR)
Cognitive function (EFF)
Cost effectiveness compared to alternatives (ECO)
Potential impact on plasma derivative market (ORG/Medico-legal)
Impact on family and carers (SOC)
Appropriateness of use in relation to solidity of evidence(ETH)
Like all dementias, Alzheimer’s Disease is an important global public health problem.
Immunoglobulins, traditionally used to prevent or treat infectious diseases have been recently used for other non-communicable conditions including rare neurological diseases.
We report on reviews of the evidence of use and effect of immunoglobulins for Alzheimer’s Disease and Mild Cognitive Impairment.
The existence and significance of Mild Cognitive Impairment are still debated
Health Problem and Current Use of the Technology (CUR)
Alzheimer’s Disease is an important public health problem, like all dementias. The existence and significance of Mild Cognitive Impairment are still debated
Description and technical characteristics of technology (TEC)
Immunoglobulins have been tradionatioally used for passive immunisation against infectious diseases, although in the last decades their use has expanded to include blood disorders, rare neurological disorders and cancer. Safety of the technology (SAF)
Effectiveness of the technology (EFF)
Despite several placebo controlled trials having been carried out and completed and some being underway so far there is no evidence of either positive or negative impact of IVIG on Alzheimer’s Disease or Mild Cognitive Impairment.
Costs and economic evaluation (ECO)
In the absence of any discernible difference against placebo, no estimates of a trade-off between costs and benefits can be made at present.
Ethical aspects of the technology (ETH)
The only foreseeable ethical aspect which could be raised by the granting of a MA are the effects of industrial production on the limited supply of blood products used to treat other conditions such as clotting disorders.
Organisational aspects of the technology (ORG)
In the absence of any discernible difference against placebo, no estimates of organisational impact can be made at present
Social aspects of the technology (SOC)
In the absence of any discernible difference against placebo the social aspects cannot be defined
Legal aspects of the technology (LEG)
In the absence of any discernible difference against placebo the legal aspects cannot be defined
The data gathered and synthetized in this Core HTA show that at present there is little evidence of any effect (positive or negative) of IVIG on Alzheimer’s Disease and Mild Cognitive Impairment. Although the evidence base is still small and several trials are still to be completed or reported, the persisting speculative nature of the pathogenesis of dementia and consequent mechanism of action of any biological product suggest that investment in research of causation might be a better priority.
This is the second of our three JA2 scheduled pilot projects. We have experienced several hitherto unforeseen difficulties during the development of the project.
The first problem was related to the aftermath of choice of topic. There is little doubt that dementias are an important topic but we were also aware of the potential demands on plasma derivatives for the manufacture of IVIG. This would have a major influence in a delicately balanced market with many highly motivated patient organisations. Choice of an inert comparator, although dictated by the early phase of experimentation of AD IVIG, was also not a traditional choice in any HTA activity and much discussed. The choice has left unresolved disagreements.
The pre-Market Authorisation Application (MAA) nature of the intervention being assessed also meant that many trials were ongoing or unpublished, even if completed. This carried many implications which added to the difficulties. Data were either not available or were made available indirectly on registers such as clinicaltrials.gov after our manufacturer enquires drew a blank. Register “publication” took place in the autumn of 2014, long after completion of our primary searches in February 2014. Although data were quantitatively plentiful, they lacked detailed description of methods and a full study protocol which made its very inclusion and interpretation contentious. The difficulties came to a head with two distinct points of view regarding the inclusion of data after the main search had taken place. Some investigators were worried about risk of bias being introduced in the assessment, others thought the importance of reporting the largest trial ever conducted (yet inexplicably unpublished two years from completion) to be paramount.
To manage the problems, Coordination asked the Editorial Team for guidance. The Team, made up of all PIs, decided to allow inclusion of the register data. However, to minimize the risk of introducing bias by secondary searching (i.e. post primary search in February 2014) of only two domains, the Team recommended the conduct of an update search for all other domains to coincide with the date of the secondary search of registers. Although the secondary search did not identify any new additional evidence, it generated additional work, further delay and dissatisfaction with the composition of the Team as all members of the domains on which the discussion centered wanted a say.
Several positive points arise from this experience. First, it is clear that the management infrastructure and input were insufficient to deal with the complexity and novelty of the work. Second, few members of the team had experience in dealing with what were essentially unpublished data. Third, the topic proved to be a good testing ground for dealing with unexpected problems. The experience gained should be reflected in future procedures.
The Core Model is not intended to provide a cookbook solution to all problems but to suggest a way in which information can be assembled and structured, and to facilitate its local adaptation. The information is assembled around the nine domains, each with several result cards in which questions and possible answers are reported.
The reasons for having a standardised but flexible content and layout are rooted in the way HTA is conducted in the EU and in the philosophy of the first EUnetHTA Joint Actions production experiment.
HTA is a complex multidisciplinary activity addressing a very complex reality – that of healthcare. Uniformly standardised evidence-based methods of conducting assessments for each domain do not exist1. There are sometimes variations across and within Member States in how things are done and which aspects of the evaluation are privileged. This is especially so for the “softer” domains such as the ethical and social domains.
This pilot represents a useful lesson for methodological development in EUnetHTA Joint Action 2.