As the treatment paradigm in inflammatory bowel disease (IBD) has shifted from controlling symptoms to fully controlling disease in order to prevent organ damage and disability, some have argued that disability is a better, more objective measure than quality of life in clinical trials and population studies of IBD.
As the treatment paradigm in inflammatory bowel disease (IBD) has shifted from controlling symptoms to fully controlling disease in order to prevent organ damage and disability, some have argued that disability is a better, more objective measure than quality of life in clinical trials and population studies of IBD.
A November 2017 review in Therapeutic Advances in Gastroenterology by Patrick B. Allen, MD, and colleagues investigated measuring disability in IBD, defined in 2001 by the World Health Organization (WHO) in its International Classification of Functioning, Disability and Health (ICF) as “any restriction or lack (resulting from impairment) of ability to perform an activity in the manner or within the range considered normal for a human being.”
IBD is known to affect physical, psychological, familial, and social dimensions of life; the psychological impact of IBD may also contribute to disability. While experience with rheumatoid arthritis (RA) and multiple sclerosis (MS) has shown that disability can be prevented by disease-modifying drugs, such evidence is currently lacking in IBD. The review points out that WHO’s validated disability index can be used to explore whether disability can also be prevented in IBD.
In 2007 the IBD Disability Index (IBD-DI) was developed in collaboration with WHO and was validated in a French population-based study. The IBD-DI demonstrated high internal consistency, interobserver reliability and construct validity, and moderate intraobserver reliability. The IBD-DI is used mainly in the clinical trial setting because it evaluates functional status. A shortened, self-administered adaptation of the validated IBD-DI known as the IBD Disk was more recently developed to permit immediate visual representation of patient-reported disability markers such as sleep, sexual function, abdominal pain, body image, and energy. The disk lacks validation, but has the potential to be a valuable outcome measure for use during routine clinical visits.
Dr. Allen and colleagues performed a literature search through June 2017 using keywords pertaining to IBD and searched abstracts from the annual meetings of the major gastroenterology groups. Many studies and questionnaires about IBD primarily focused on subjective measures of disease. Fatigue and pain were found to be commonly reported symptoms in patients with IBD. A large proportion of patients were found to require opioid analgesia, and patients with IBD were reported to experience frequent and concomitant anxiety and depression. Overall, disability was found to be high in both Crohn disease and ulcerative colitis and to contribute to disease burden in IBD.
The review concludes that disability is prevalent in IBD and is seen in patients with ulcerative colitis (UC) before and after surgery and in Crohn disease (CD). “The IBD-DI should become a major secondary endpoint in clinical trials,” the review authors state. “This index needs to be expanded to include worldwide comparisons of disability among IBD patients in a longitudinal fashion.”
Future clinical trials will move away from simply targeting response and remission to ensure deep remission, improvement in defined patient-reported outcomes, and ultimately preventing and improving disability in IBD, the review concludes. “The costs and safety of these new therapeutic strategies in IBD that are being developed to change the natural history of disease with earlier and effective treatments in order to reduce long-term disability in IBD patients, remain to be established.”
The Top 5 Most-Read Gastroenterology Articles of 2024
December 21st 2024The top gastroenterology biosimilar news from 2024 highlight fluctuations in the adalimumab biosimilar market throughout the year, while FDA and European approvals for ustekinumab biosimilars are set to improve access and reduce costs for patients with Crohn disease and ulcerative colitis.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
13 Strategies to Avoid the Nocebo Effect During Biosimilar Switching
December 18th 2024A systematic review identified 13 strategies, including patient and provider education, empathetic communication, and shared decision-making, to mitigate the nocebo effect in biosimilar switching, emphasizing the need for a multifaceted approach to improve patient perceptions and therapeutic outcomes.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Stable Patient Satisfaction Found After Switching From the Humira or Biosimilar CT-P17
December 14th 2024A real-world study in France found patient satisfaction was stable after switching from either the reference product or a low-concentration adalimumab biosimilar to the adalimumab biosimilar CT-P17, a high-concentration, citrate-free formulation.
Eye on Pharma: Golimumab Biosimilar Update; Korea Approves Denosumab; Xbrane, Intas Collaboration
December 10th 2024Alvotech and Advanz Pharma have submitted a European marketing application for their golimumab biosimilar to treat inflammatory diseases, while Celltrion secured Korean approval for denosumab biosimilars, and Intas Pharmaceuticals partnered with Xbrane Biopharma on a nivolumab biosimilar.