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1.
Ann Rheum Dis ; 82(5): 594-598, 2023 05.
Article in English | MEDLINE | ID: mdl-36702529

ABSTRACT

To detail the unmet clinical and scientific needs in the field of rheumatology. After a 2-year hiatus due to the SARS-CoV-2 pandemic, the 22nd annual international Advances in Targeted Therapies meeting brought together more than 100 leading basic scientists and clinical researchers in rheumatology, immunology, epidemiology, molecular biology and other specialties. Breakout sessions were convened with experts in five rheumatological disease-specific groups including: rheumatoid arthritis (RA), psoriatic arthritis, axial spondyloarthritis, systemic lupus erythematosus and connective tissue diseases (CTDs). In each group, experts were asked to identify and prioritise current unmet needs in clinical and translational research, as well as highlight recent progress in meeting formerly identified unmet needs. Clinical trial design innovation was emphasised across all disease states. Within RA, developing therapies and trials for refractory disease patients remained among the most important identified unmet needs and within lupus and spondyloarthritis the need to account for disease endotypes was highlighted. The RA group also identified the need to better understand the natural history of RA, pre-RA states and the need ultimately for precision medicine. In CTD generally, experts focused on the need to better identify molecular, cellular and clinical signals of early and undifferentiated disease in order to identify novel drug targets. There remains a strong need to develop therapies and therapeutic strategies for those with treatment-refractory disease. Increasingly it is clear that we need to better understand the natural history of these diseases, including their 'predisease' states, and identify molecular signatures, including at a tissue level, which can facilitate disease diagnosis and treatment. As these unmet needs in the field of rheumatic diseases have been identified based on consensus of expert clinicians and scientists in the field, this document may serve individual researchers, institutions and industry to help prioritise their scientific activities.


Subject(s)
Arthritis, Psoriatic , Arthritis, Rheumatoid , COVID-19 , Rheumatic Diseases , Rheumatology , Humans , SARS-CoV-2 , Rheumatic Diseases/drug therapy , Rheumatic Diseases/diagnosis , Arthritis, Rheumatoid/drug therapy , Arthritis, Psoriatic/drug therapy
2.
Ann Rheum Dis ; 79(1): 39-52, 2020 01.
Article in English | MEDLINE | ID: mdl-31413005

ABSTRACT

To update the European League Against Rheumatism (EULAR) recommendations for vaccination in adult patients with autoimmune inflammatory rheumatic diseases (AIIRD) published in 2011. Four systematic literature reviews were performed regarding the incidence/prevalence of vaccine-preventable infections among patients with AIIRD; efficacy, immunogenicity and safety of vaccines; effect of anti-rheumatic drugs on the response to vaccines; effect of vaccination of household of AIIRDs patients. Subsequently, recommendations were formulated based on the evidence and expert opinion. The updated recommendations comprise six overarching principles and nine recommendations. The former address the need for an annual vaccination status assessment, shared decision-making and timing of vaccination, favouring vaccination during quiescent disease, preferably prior to the initiation of immunosuppression. Non-live vaccines can be safely provided to AIIRD patients regardless of underlying therapy, whereas live-attenuated vaccines may be considered with caution. Influenza and pneumococcal vaccination should be strongly considered for the majority of patients with AIIRD. Tetanus toxoid and human papilloma virus vaccination should be provided to AIIRD patients as recommended for the general population. Hepatitis A, hepatitis B and herpes zoster vaccination should be administered to AIIRD patients at risk. Immunocompetent household members of patients with AIIRD should receive vaccines according to national guidelines, except for the oral poliomyelitis vaccine. Live-attenuated vaccines should be avoided during the first 6 months of life in newborns of mothers treated with biologics during the second half of pregnancy. These 2019 EULAR recommendations provide an up-to-date guidance on the management of vaccinations in patients with AIIRD.


Subject(s)
Antirheumatic Agents/therapeutic use , Autoimmune Diseases/drug therapy , Bacterial Infections/prevention & control , Rheumatic Diseases/drug therapy , Vaccines/therapeutic use , Virus Diseases/prevention & control , Family Characteristics , Hepatitis A/prevention & control , Hepatitis A Vaccines/therapeutic use , Hepatitis B/prevention & control , Hepatitis B Vaccines/therapeutic use , Herpes Zoster/prevention & control , Herpes Zoster Vaccine/therapeutic use , Humans , Influenza Vaccines/therapeutic use , Influenza, Human/prevention & control , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/therapeutic use , Pneumococcal Infections/prevention & control , Pneumococcal Vaccines/therapeutic use , Tetanus/prevention & control , Tetanus Toxoid/therapeutic use , Vaccines, Attenuated/therapeutic use
3.
Ann Rheum Dis ; 79(1): 88-93, 2020 01.
Article in English | MEDLINE | ID: mdl-31662322

ABSTRACT

OBJECTIVES: To detail the greatest areas of unmet scientific and clinical needs in rheumatology. METHODS: The 21st annual international Advances in Targeted Therapies meeting brought together more than 100 leading basic scientists and clinical researchers in rheumatology, immunology, epidemiology, molecular biology and other specialties. During the meeting, breakout sessions were convened, consisting of 5 disease-specific groups with 20-30 experts assigned to each group based on expertise. Specific groups included: rheumatoid arthritis, psoriatic arthritis, axial spondyloarthritis, systemic lupus erythematosus and other systemic autoimmune rheumatic diseases. In each group, experts were asked to identify unmet clinical and translational research needs in general and then to prioritise and detail the most important specific needs within each disease area. RESULTS: Overarching themes across all disease states included the need to innovate clinical trial design with emphasis on studying patients with refractory disease, the development of trials that take into account disease endotypes and patients with overlapping inflammatory diseases, the need to better understand the prevalence and incidence of inflammatory diseases in developing regions of the world and ultimately to develop therapies that can cure inflammatory autoimmune diseases. CONCLUSIONS: Unmet needs for new therapies and trial designs, particularly for those with treatment refractory disease, remain a top priority in rheumatology.


Subject(s)
Clinical Trials as Topic , Lupus Erythematosus, Systemic/drug therapy , Research Design , Rheumatic Diseases/drug therapy , Arthritis, Psoriatic/drug therapy , Arthritis, Psoriatic/physiopathology , Arthritis, Rheumatoid/drug therapy , Arthritis, Rheumatoid/physiopathology , Biomedical Research , Central Nervous System Sensitization , Congresses as Topic , Humans , Lupus Erythematosus, Systemic/physiopathology , Molecular Targeted Therapy , Needs Assessment , Research , Rheumatic Diseases/physiopathology , Rheumatology , Spondylitis, Ankylosing/drug therapy , Spondylitis, Ankylosing/physiopathology
5.
Clin Exp Rheumatol ; 34(4 Suppl 98): 69-76, 2016.
Article in English | MEDLINE | ID: mdl-27586809

ABSTRACT

The 18th annual international Targeted Therapies meeting brought together over 100 leading scientists and clinicians from around the world in the field of rheumatology. During the meeting, breakout sessions were held consisting of 5 disease-specific groups each with 20-40 experts assigned to each group based on clinical or scientific expertise. Specific groups included: rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis/spondyloarthritis, systemic lupus erythematous, and other connective tissue diseases (e.g. Sjögren's, Behçet's, others). In each group, experts were asked to identify unmet needs in 3 categorical areas: basic/translational science, clinical science and therapeutic development, and clinical care. Needs were prioritised as primary or secondary. Overall, similar primary unmet needs were identified within each disease foci. Within translational science, these included the need for better understanding the heterogeneity within each disease, such that predictive tools for therapeutic response could be developed. Within clinical science and therapeutic trials, the ability to prevent progression to disease onset in those at risk, and the ability to cure disease were identified. A further unmet need was to develop new and accessible therapeutics, as well as to conduct strategic trials of currently approved therapies. Within the clinical care realm, improved co-morbidity management and patient-centered care were identified as unmet needs. Lastly, it was strongly felt there was a need to develop a scientific infrastructure for well-characterised, longitudinal cohorts married with biobanks and mechanisms to support data-sharing. This infrastructure could facilitate many of the unmet needs identified within each disease area.


Subject(s)
Antirheumatic Agents/therapeutic use , Biomedical Research , Molecular Targeted Therapy , Rheumatic Diseases/drug therapy , Rheumatology , Animals , Antirheumatic Agents/adverse effects , Disease Progression , Health Priorities , Humans , Needs Assessment , Remission Induction , Research Design , Rheumatic Diseases/diagnosis , Rheumatic Diseases/immunology , Treatment Outcome
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