Behçet’s disease (BD) is an autoinflammatory disease that can affect multiple organs, including the gastrointestinal tract. Conventional management comprises anti-inflammatory drugs such as glucocorticoids (GCs) and/or immunomodulators that alleviate symptoms. The introduction of biological agents that target tumor necrosis factor α (TNF-α) has improved disease management. The goal of this work was to analyze the current prevalence and incidence of total BD and gastrointestinal Behçet’s disease (GIBD) in Japan, and examine treatment trends, especially regarding the use of TNF-α inhibitors (TNFαi).
Methods
We performed a retrospective descriptive observational study in which BD and GIBD demographic trends, medical treatment patterns, and reported adverse events (AEs) were assessed among patients with data recorded between 2017 and 2021 in the Japan Medical Data Center Claims Database (now JMDC Inc.).
Results
Prevalence of BD and GIBD in Japan during the observation period increased at an annual rate of + 3% and + 4%, respectively, while incidence decreased by − 5% and − 2%, with a more prominent decline in confirmed GIBD cases (− 15%). Although GCs were the most common initial treatment administered, use of TNFαi for BD and GIBD management increased by + 5.6% and + 8.1%, respectively. Severe AEs (mainly pneumonia and GI-associated AEs) were reported in 40% of patients receiving TNFαi; however, a high retention rate (of up to 80%) was observed 3 years after treatment initiation.
Conclusion
The use of TNFαi for GIBD treatment has increased in Japan in recent years. Additional research is necessary to further evaluate TNFαi effectiveness in GIBD and other BD subtypes.
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Introduction
Behçet’s disease (BD) is an autoinflammatory disease that affects multiple parts of the body [1‐3]. Typical clinical features include oral and urogenital ulcers, as well as ocular and cutaneous lesions. Others include vascular, articular, neurological, and gastrointestinal (GI) manifestations [3].
Although the cause of BD is not currently known, both genetic and environmental factors play a role in disease pathogenesis. Genome-wide studies have identified multiple genes involved in the immune response as susceptibility factors, including HLA-B51, which is associated with the strongest predisposition. HLA-B51 expression varies depending on sex, with carriers being predominantly male [4, 5], and is associated with a higher incidence of ocular manifestations and lower prevalence of GI involvement, while its relation to genital ulceration remains unclear [4‐8].
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Environmental factors, such as geographical variation, have also been shown to impact BD frequency. BD exhibits a high prevalence in areas encompassing the Mediterranean Sea, the Middle East, and East Asia (China, Korea, and Japan), with the most significant occurrence found in Türkiye [9]. These regions also have the highest association between HLA-B51 and BD [8].
As there is currently no cure for BD, the primary goal of treatment is to alleviate symptoms and manage disease progression and severity [3, 10]. With anti-inflammatory agents, such as glucocorticoids (GCs) and/or immunosuppressants, these strategies focus on controlling inflammation, preventing irreversible tissue damage, and avoiding life-threatening complications [3, 11]. Targeting tumor necrosis factor α (TNF-α) with biological agents has made a substantial contribution to disease management, particularly in patients with severe organ involvement or resistance to conventional medications [12, 13].
Gastrointestinal Behçet’s disease (GIBD) is one of the most severe subtypes of BD and is associated with higher morbidity and mortality [3]. Data from different epidemiological studies suggest that between 15% and 50% of patients with BD in Japan have GI involvement [7, 14]. Patients suffering from GIBD present with lesions in the GI tract, most commonly located in the terminal ileum and ileocecal region. These lesions lead to abdominal pain, vomiting, weight loss, diarrhea, and bloody stool, with major complications that include intestinal bleeding and perforation [2, 14, 15]. TNF-α inhibitors (TNFαi) adalimumab and infliximab were approved for GIBD management in Japan in 2013 and 2015, respectively, and use for patients who fail to respond to conventional treatments has been incorporated into recent updates of the Japanese BD guidelines [12, 16‐19].
The aim of this study was to analyze the prevalence and incidence of BD and GIBD and assess treatment patterns, especially the use of biologic agents (TNFαi), in these indications among patients in Japan with data recorded in the Japan Medical Data Center Claims Database (now JMDC Inc.).
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Methods
We conducted a retrospective descriptive observational study using the JMDC Claims Database (study period: 2017–2021). This repository includes data from multiple employee-based health insurance firms, covering civil servants, those employed in the private sector, and their respective families, and represents one of the major datasets for the working-age population in Japan [20]. Approximately 14,000,000 patients were included in this database as of 2022, accounting for about 10% of the Japanese population.
The database provides individual-level patient and clinical information, including demographics, date-stamped inpatient, and outpatient health insurance claims (using disease names for insurance purposes), diagnosis coded using the International Statistical Classification of Diseases and Related Health Problems, 10th revision [ICD-10], procedures, prescriptions, medical services, costs, and medical institutions, as well as health check-up records for some individuals [20].
No ethics approval from an institutional review board was required, as the study used pre-existing, anonymized data whose identifiable personal information could not be reconstructed. The study was, therefore, considered to be outside the scope of the Japanese Ethical Guidelines for Medical and Health Research Involving Human Subjects. In addition, no informed consent from the individuals included in this study was required, as all personal and site information were anonymized by JMDC Inc.
Patients were included in the study when they met the following criteria: recorded diagnosis of BD during the study period, as per the ICD-10 coding (M35.2). The cohort of patients who had at least one confirmed M35.2 diagnosis was considered for the prevalence and incidence analysis. Suspected cases were initially identified by symptom-based codes (e.g., codes for oral ulcers, ocular inflammation), but were not directly coded as M35.2 until further evaluation confirmed the diagnosis. Symptoms used to supplement the GIBD subtype were intestinal ulcer (ICD-10 code K633) and GI bleeding. BD subtype definition and drugs included in this study are described in Table 1.
Table 1
Definition of BD subtypes (a) and drugs included in the study (b)
(a) Definition of BD subtypes
BD subtype
Disease code
Total BD
M35.2a
No specific BD subtype
Articular feature
Incomplete feature
8846052
Ocular feature
8845881
Oral feature
1361010
Genital feature
1361011
Specific BD subtype
GI feature
8842203
Neurological feature
1361005
Vascular feature
1361009
(b) Drugs used
Biologics
TNFαi
Adalimumab and infliximab
Non-biologics
GCs
Prednisolone and systemic GCs (H02A)
CNi
Tacrolimus hydrate
Immunomodulators
AZA, mercaptopurine hydrate, MTX and ciclosporin A
Other
Apremilast, 5-ASA and colchicine
5-ASA, 5-aminosalicylic acid; AZA, azathioprine; BD, Behçet’s disease; CNi, calcineurin inhibitors; GCs, systemic glucocorticoids; GI, gastrointestinal; ICD-10, International Statistical Classification of Diseases and Related Health Problems, 10th revision; MTX, methotrexate; TNFαi, TNF-α inhibitors
aICD-10 code M35.2 is used for BD diagnosis, while subtypes are defined via specified disease codes
Data analyses were performed with the intent-to-collect information on BD and GIBD prevalence and incidence as well as drug treatment patterns within the database, with special focus on TNFαi use and reported adverse events (AEs). Assessments were performed per fiscal year (FY), which comprised the period between April of the indicated year and March of the following year (e.g., FY2021 included data from April 2021 to March 2022). Some analyses were conducted for a single FY, while others compare over time dating back to 2017 or 2019, as indicated in each section and figure.
Prevalence and incidence were calculated as follows:
Prevalence: simple annual aggregation by age/sex.
Incidence: first M35.2 diagnosis in each patient was counted and patients who had any BD diagnosis within the first 6-month window in their medical record were excluded from the count, to ensure first diagnoses within the dataset.
Scaling: patient counts for prevalence and incidence were scaled up to enable sizing of the Japanese BD patients and a scaling algorithm was applied to each sex and age segment to obtain estimates for 100% of the Japanese population.
Results
BD and GIBD demographics
BD subtypes, age, and sex distribution
According to the JMDC dataset, 415 of 1993 patients diagnosed with BD during FY2021 had a specific BD subtype (GI, neurological, and vascular) (21%), with the most common being GIBD (14%) (Table 2). A high proportion of patients diagnosed with both BD and GIBD during FY2021 were ≥ 60 years of age (43.9% and 37.5%, respectively). The GIBD population was younger than the BD patient population (Fig. 1a), while there was a slightly higher proportion of female patients in both the BD and GIBD populations (59.1% and 54.3%, respectively) (Fig. 1b).
Table 2
Number of patients in the JMDC dataset diagnosed with a specific BD subtype
Number of patients with BD (%)a
Total BD
1993 (100)
No specific BD subtype
1578 (79)
Articular feature
1244 (62)
Incomplete feature
200 (10)
Ocular feature
87 (4)
Oral feature
25 (1)
Genital feature
22 (1)
Specific BD subtype
415 (21)
GI feature
278 (14)
Neurological feature
101 (5)
Vascular feature
36 (2)
BD, Behçet’s disease; GI, gastrointestinal; JMDC, Japan Medical Data Center Claims
aPercentages may not add up to 100 due to rounding
Fig. 1
Demographics. BD and GIBD patient distribution according to age (a) and sex (b) in FY2021. Percentages may not add up to 100 due to rounding. Raw number is scaled to national level based on age and sex adjustment. BD, Behçet’s disease; FY, fiscal year; GI, gastrointestinal; GIBD, gastrointestinal Behçet’s disease
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BD and GIBD prevalence and incidence
During FY2021, there were a total of 33,943 patients with BD and 6044 patients with GIBD (including suspected cases) captured in the JMDC dataset, with over half of newly diagnosed BD patients (1797 out of 3396) having GIBD (Fig. 2). In general, BD prevalence in the database increased at an annual rate of + 3% between FY2017 and FY2021, while incidence decreased at an annual rate of − 5% (Fig. 2a). In contrast, although GIBD prevalence increased by + 4% between FY2017 and FY2021, it decreased by − 2% in the latest year, while incidence decreased at an annual rate of − 1.7% between FY2017 and FY2021 (Fig. 2b). Confirmed GIBD cases comprised 486 out of a total 1797 BD cases in FY2021 (Fig. 2c). 54% of patients with GIBD captured in the database between FY2017 and FY2021 had a confirmed diagnosis within 1 month after the first BD diagnosis, while 81% were confirmed within 3 months. In addition, the prevalence of confirmed GIBD cases decreased by − 3% from FY2020 to FY2021, while the incidence declined at a pronounced annual rate of − 15% between FY2017 and FY2021 (Fig. 2c).
Fig. 2
BD and GIBD prevalence and incidence. Prevalence and incidence of total BD (a), GIBD (including suspected cases (b) and GIBD (only confirmed cases) (c) between FY2107 and FY2021, as captured in the JMDC dataset. Raw number is scaled to national level based on age and sex adjustment. BD, Behçet’s disease; FY, fiscal year; GIBD, gastrointestinal Behçet’s disease; JMDC, Japan Medical Data Center Claims
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BD treatment patterns
Treatment in GIBD vs. non-GIBD
Medical management was compared for patients with GIBD vs. non-GIBD (including other BD subtypes excluding GI involvement) over 3 years (FY2019–FY2021). Apremilast, systemic GCs (oral or intravenous), colchicine, 5-aminosalicylic acid (5-ASA), calcineurin inhibitors (CNi), TNFαi (adalimumab and infliximab), and other immunomodulators [including azathioprine (AZA), mercaptopurine hydrate, methotrexate (MTX), and ciclosporin A] were used to treat both subgroups, with immunomodulators, TNFαi, and 5-ASA use being substantially higher in patients with GIBD vs. those with non-GIBD (29% vs. 14%; 49% vs. 13%; 54% vs. 11%, respectively) (Fig. 3a). CNi and apremilast use was generally limited, suggesting a subordinate role in BD treatment in this population.
Fig. 3
Drug usage. Comparison of drug usage ratio [including apremilast, SGCs (oral or intravenous), colchicine, 5-ASA, CNi, TNFαi, and other immunomodulators] between patients with GIBD and non-GIBD (a) and line distribution by treatment among GIBD patients (b), between FY2019 and FY2021. 5-ASA, 5-aminosalicylic acid; CNi, calcineurin inhibitors; GIBD, gastrointestinal Behçet’s disease; SGCs, systemic glucocorticoids; TNFαi, TNF-α inhibitors
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Approximately 40% of patients with GIBD were on line 3–5 of treatment, compared with only ~ 15% of patients with non-GIBD. While systemic GCs, 5-ASA, and colchicine were typically administered as earlier lines of treatment (first and second), TNFαi and other immunomodulators were commonly initiated as later lines (third and fourth, respectively). In particular, 42% of TNFαi treatment for patients with GIBD was initiated as third-line therapy (Fig. 3b).
Use of TNFαi biologics
According to the JMDC dataset, adalimumab use in Japanese patients with GIBD was slightly higher than infliximab use during FY2021 (55% vs. 45%). During FY2021, there were a total of 4645 patients with BD and 1809 patients with confirmed GIBD receiving TNFαi biologics, with 627 and 228 of those treated with a TNFαi for the first time, respectively. Use of TNFαi biologics in all patients with BD increased at an annual rate of + 5.6% between FY2017 and FY2021, while for patients receiving TNFαi treatment for the first time, it remained constant (Fig. 4a). TNFαi biologic use showed a + 8.1% and a + 7.4% increase between FY2017 and FY2021 for all patients with GIBD and those receiving a TNFαi for the first time, respectively (Fig. 4b). In parallel, GC use showed a − 6.3% and a − 8.2% decrease between FY2017 and FY2021 for these groups of patients.
Fig. 4
TNFαi biologics trends. TNFαi use for BD (a) and GIBD (confirmed cases only) (b) between FY2107 and FY2021, as captured in the JMDC dataset. aN is small (10‒15), causing potential deviations. BD, Behçet’s disease; FY, fiscal year; GIBD, gastrointestinal Behçet’s disease; JMDC, Japan Medical Data Center Claims
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Use of biologic agents, adalimumab and infliximab, was highest among the GI (48%) and ocular (41%) BD subtypes, while for other forms of BD, such as vascular, oral, and neurological BD, treatment with TNFαi biologics was below 25% (Fig. 5a). In addition, treatment with biologics was lower in elderly patients with confirmed GIBD compared with younger patients. While over 50% of patients < 50 years of age received TNFαi biologics, only 38% and 14% of patients aged 50–59 and ≥ 60 years, respectively, received this treatment option (Fig. 5b). In general, TNFαi were prescribed to 48.2% of patients with confirmed GIBD, whereas biologic medication was rarely used to treat suspected cases (6.7%) (Fig. 5b). Moreover, use of biologics was particularly high in patients with confirmed GIBD and rheumatoid arthritis (RA) symptoms; 67% of patients experiencing these symptoms used TNFαi vs. 42% for those without RA symptoms.
Fig. 5
TNFαi biologics according to BD subtype and age. Use of TNFαi by BD subtype (a) and in patients with GIBD, depending on age and GIBD confirmed/suspected status (b), in FY2021. aAge/gender adjusted to the national population in Japan. BD, Behçet’s disease; FY, fiscal year; GI, gastrointestinal; GIBD, gastrointestinal Behçet’s disease; TNFαi, TNF-α inhibitors
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TNFαi switching and co-medication
During their course of treatment, patients with GIBD may switch between TNFαi infliximab and adalimumab. In FY2021, 17.3% of patients were receiving treatment with a second TNFαi, with 5.2% of patients having switched from one TNFαi to the other during this period.
Patients may also receive a combination of treatments. During FY2021, only 18% of patients with GIBD received TNFαi treatment as monotherapy, while others received TNFαi in combination with GCs, 5-ASA, and/or immunomodulators (Fig. S1). The proportion of patients receiving TNFαi as a monotherapy was 16% when considering GCs as prednisolone only vs. 12% when expanding the definition to systemic GCs. Independent of the GC definition, most patients (81%) continued TNFαi treatment, with few initiating (5–6%) or discontinuing (13–14%) this treatment. In addition, over 90% of patients that discontinued TNFαi treatment continued taking other medications, with GCs (42%) and other immunomodulators (17%) as the most common options.
TNFαi treatment assessment
TNFαi biologic treatment initiation and duration
A total of 22% of patients in the JMDC dataset initiated TNFαi treatment prior to a formal GIBD diagnosis, while 64% received biologics within 1 month of a confirmed diagnosis. Patients using TNFαi between FY2017 and FY2019 showed a high level of adherence to the treatment, with 83% and 78% of patients remaining on treatment at 1 and 3 years after TNFαi initiation, respectively. Only 5.1% and 4.3% of patients with BD and GIBD, respectively, discontinued TNFαi treatment per year between FY2019 and FY2021.
AEs associated with TNFαi treatment
Analyses of patients with GIBD receiving TNFαi biologics during FY2021 revealed that 40% experienced severe AEs. These included pneumonia (32%), GI AEs (15%), sepsis (5%), and intestinal perforation (2%). Several risk factors were associated with severe GI AEs, such as more advanced age, female sex, GIBD subtype, and earlier therapy lines or first-time exposure to biologic agents. In addition, 8.2% of patients who received TNFαi treatment underwent surgery during FY2021.
Discussion
Our study presents an overview of BD and GIBD incidence over time and the current treatment landscape for the Japanese working-age population and their families captured in the JMDC Claims Database. Accordingly, a scaling algorithm was applied where appropriate to reflect the age and gender structure of the general Japanese population.
With over 30,000 patients, the JMDC database included a significantly higher number of patients with BD in FY2021 than the 20,035 people who received medical care for BD in 2014, according to the Ministry of Health, Labour, and Welfare [21]. These discrepancies can possibly be attributed to the inclusion of suspected or mild cases in the database. GIBD was the most common subtype (14%) detected among patients with BD during FY2021. Surprisingly, during this time, more than half of newly diagnosed patients presented with GI involvement (1797 out of 3396 patients). In Japan, a substantially high proportion of GIBD has been reported in the past. Although prevalence and incidence rates vary considerably between studies (12–50%) [14], caution should be exercised when comparing and interpreting the data in terms of timing (study conduct and observation period), source of data collection (e.g., registry, database vs. individual hospital/institution), patient characteristics (e.g., age, sex, disease onset), and geographical aspects. The data may also vary due to different and evolving diagnostic criteria applied, distinct clinical disciplines involved (e.g., gastroenterology, rheumatology), or misdiagnosis (i.e., lack of consideration of differential diagnoses such as Crohn’s disease or ulcerative colitis).
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Slightly more female patients diagnosed with BD and GIBD were captured in the JMDC Claims Database, which was in accordance with other studies in Japanese and Korean populations [22, 23]. Further evidence from other Asian cohorts (from Türkiye and China) showed a more similar proportion of male and female patients with BD and GIBD, with a slightly higher proportion of males in the Chinese study [24, 25].
As described in previous studies, the frequency of patients with GI involvement reported in the JMDC Claims Database is higher than that of other regions from East Asia. Although countries such as Türkiye or Korea have a generally high BD incidence, only a small proportion of patients were reported to present GI lesions [2, 14]. In contrast, in other cohorts from Russia, the US, or the UK, which are known to have a lower BD incidence, a larger proportion of GIBD cases was observed [2, 14]. However, these data must be interpreted with caution, considering the different regional diagnostic criteria, and the possibility of misdiagnoses due to the lack of endoscopic assessments [14].
While GIBD might not be the most common BD subtype in other regions, an increasing trend in the presence of GI manifestations has been described in other Japanese and Korean studies. Research by Soejima and colleagues, who analyzed the clinical clusters contributing to the evolution of BD in Japan between 1991 and 2014, was based on data from a hospital-based regional BD registry as well as the Japanese national BD registry [7]. In this study, an increase in GI involvement in BD was observed, particularly after 2010 [7]. A similar trend regarding GI manifestations was also found in a Korean study, which analyzed a large hospital-based patient BD registry with data gathered between 1983 and 2012 [26]. Due to the similarities in the genetic backgrounds and previous diagnostic criteria in these countries [27], it is possible that at least some factors contributing to the prevalence of GI involvement in patients from East Asia are environmental. Interestingly, the adoption of a westernized lifestyle is believed to play a role in the recent expansion of other inflammatory bowel diseases in both Japan and Korea [28], which could also contribute to the predominance of GIBD.
In contrast, BD and overall GIBD incidence (including both confirmed and suspected GIBD cases) were shown to slightly decrease (annual rates of − 5% and − 1.7%, respectively) between FY2017 and FY2021, although this decline was more prominent for confirmed GIBD cases (− 15%). Changes in GIBD diagnostic parameters and therapeutic guidelines from the Japanese society for BD in 2020 [19] could be one of the key factors influencing this outcome, as the use of the proposed diagnostic algorithm is likely to help exclude false positives. These may also explain the discrepancies observed between the suspected and confirmed GIBD cases, with the latter being potentially underestimated. Moreover, improved hygiene in Japan, particularly during the SARS-CoV-2 pandemic, may have impacted GIBD occurrence. An alternative explanation is that GIBD was potentially underdiagnosed during the SARS-CoV-2 pandemic, due to restricted access to care. Interestingly, although both the SARS-CoV-2 virus and the COVID-19 vaccines have the potential to lead to systemic vasculitis, no events of BD post-infection or vaccination have been described [29]. The potential connection between SARS-CoV-2 (especially for the pre-Omicron viral variants) and the development of some autoimmune diseases, including ulcerative colitis, has been documented; whereas, other syndromes, such as Crohn’s disease, seem to be less likely to occur after a COVID-19 infection [30]. Other reports have shown minimal disease flares upon COVID-19 vaccination for some inflammatory and rheumatic diseases [31‐33].
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The extended use of TNFαi for BD treatment, as well as for other diseases (e.g., Crohn’s disease or ulcerative colitis), may have impacted the management of BD and its evolution. TNFαi administration increased both for BD and GIBD between FY2017 and FY2021 (annual rates of + 5.6% and + 8.1%, respectively). In particular, during FY2021, adalimumab use was slightly higher than infliximab, which could be due to infliximab being approved at a later timepoint than adalimumab for this indication [12, 16‐19]. Compared with other subtypes, treatment with TNFαi biologics was highest for GIBD (48%), although it was observed that TNFαi were mainly prescribed to patients with confirmed GIBD, while they were less frequently used to treat suspected GIBD cases. A differential diagnosis of GIBD is complex due to similarities with other disorders, such as inflammatory bowel syndrome, Crohn’s disease, and ulcerative colitis [34], as well as simple ulcers in the GI tract, but a correct diagnosis is essential to ensure access to and maximum benefit from appropriate therapies [10].
Aside from the BD subtype, another aspect that was shown to influence the use of TNFαi was the medication previously used. TNFαi treatment for GIBD was often initiated in the third-line setting (in 42% of cases), which suggests that patients who receive TNFαi may be heavily pre-treated. In addition, only 12–18% of patients received TNFαi monotherapy, while the majority was administered TNFαi in combination with GCs, 5-ASA, and/or other immunomodulators. The information captured in the JMDC Claims database reflects the use of several immunomodulators, including AZA, mercaptopurine hydrate, MTX, and ciclosporin A. While thiopurines are widely employed to manage GIBD, with their use being recommended by the Japanese BD guidelines for patients who are dependent on GCs, or for those in whom GCs and/or TNFαi are ineffective, the efficacy of MTX remains unclear, and their use as monotherapy is not advised [19, 35]. Physicians’ specialization might influence immunomodulator administration, with MTX being more commonly prescribed among rheumatologists and AZA among GI specialists.
Given the secondary effects of long-term GC use and the promising efficacy results observed with TNFαi and other biologics, these agents could potentially become a GC-sparing therapy [12]. In accordance with this, a retrospective study based on patients with ulcerative colitis captured in the JMDC Claims Database showed a decrease in the use of GCs between 2006 and 2016, as treatment with biologics increased, although inappropriate use of GCs (such as long-term regimens) still persisted [36]. A recent study demonstrated that TNFαi monotherapy, or a TNFαi in combination with reduced GC doses, showed better potential for GIBD management in terms of GI ulcer healing and relative to GC monotherapy [37]. In this study, GC use also showed a decrease between FY2017 and FY2021 for patients with GIBD, which could be attributable to the introduction of biologic agents. The initial dosage remained stable over the study period (14 mg or 15 mg prednisolone, administered for a duration of 28–34 days ± 3 days). However, the lack of information related to the GC dosage over time limits the conclusions, notably about the tapering effect, and would need additional exploration [37]. Currently, although early introduction of TNFαi is encouraged in the Japanese BD guidelines [19], GIBD treatment in Japan still relies heavily on GCs, followed by immunomodulators and TNFαi.
Reimbursement access and the costs associated with TNFαi treatment may also affect the timing of biologic use in Japan, with TNFαi only available at earlier treatment stages for severe BD cases. Reimbursement benefits were also suggested to affect biologic use in Korea [38]. Moreover, the treatment patterns between 2011 and 2014 in Korea, as described by Han and colleagues, were similar to those in Japan, with GCs being the main therapeutic option (in 53.2% of patients), followed by immunomodulators (35.6%) and TNFαi biologics (4.7%) [38].
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Treatment duration and AEs were also recorded in the JMDC Claims database. High adherence to TNFαi regimens was observed (around 80% after 3 years); however, a large proportion of patients experienced severe AEs (40%), especially related to infections. Previous systematic reviews have already identified increased vulnerability to infections as one of the main complications associated with TNFαi treatment [39‐42]. Another complication, which is related to the severity of BD and is among the main causes of morbidity and mortality, is the appearance of intestinal perforations [14, 15]. In this study, intestinal perforations were observed in 2% of patients with GIBD receiving TNFαi biologics. This shows an important decline compared to the incidence reported in earlier studies, where these occurred in up to 13–25% of patients with GIBD [15, 43, 44]. The inclusion of BD treatments other than TNFαi, such as high-dose GCs, may have contributed to the risk of developing perforations in previous research [10]. In addition, differences in the patient population recruited across studies, and their predisposition to suffer intestinal perforations, could have also affected these results.
Surprisingly, in contrast to the high proportion of patients experiencing severe AEs, only 4.3% of patients with GIBD discontinued TNFαi treatment per year. The high retention rate suggests that, aside from a high efficacy, AEs associated with TNFαi use may generally be manageable [41, 42]. Nonetheless, further analyses comprising not only the working-age population and their families, but the general population, are needed to better understand the long-term AE profile of TNFαi and other biologic agents.
It is important to address the unresolved unmet need for the small group of patients that discontinue TNFαi treatment, but who could potentially benefit from other biologic agents or alternative treatments. Previous research has identified several clinical variables as predictors for GIBD prognosis. Variables such as younger age at diagnosis, history of surgery, and lack of initial response to medication, among others, have been linked to a poor prognosis [45]. Although these factors need to be further studied to fully understand their predictive power, they may be helpful tools for a more personalized and effective care, which could especially help subgroups of patients with these unmet needs. A more complete understanding of the genetic predisposition underlying GIBD, including HLA-B51 and other genetic factors, as well as investigation of emerging treatments for GIBD management, which may involve different targets aside from TNF-α, will also contribute to achieving these goals.
Some limitations are to be considered when interpreting the JMDC data, as only patients who visit hospitals or clinics and are covered by company health insurance are captured in the dataset. Since Japanese employees tend to remain insured with the same health insurance company for several years, which assigns them a personal ID, they can be followed over various time periods, even if they are treated by different medical facilities [46, 47].
Age and sex are included in the database, but it only comprises the working-age population and their families, i.e., the elderly population (60–75 years of age) is drastically underrepresented (≤ 3% vs. ~ 9–10% for younger age groups), which is important given that the overall Japanese population is aging. Accordingly, no comparative analyses, e.g., on drug use in elderly versus younger patients with BD, can be carried out with the necessary robustness based on the JMDC data, even if these are of scientific interest. Furthermore, direct comparisons with other studies and more representative populations may need to be interpreted with caution.
Another known limitation of the JMDC is the lack of information on disease severity, extension of inflammation and treatment outcome [46]. Accordingly, this study was not designed to analyze corresponding time trends related to any of these.
Furthermore, many AEs may not be captured in the database, and may, therefore, be underrepresented. In addition, patients with multiple comorbidities, including disorders that may also respond to TNFαi treatment, have the potential to be classified under another diagnosis and, therefore, not captured in this analysis.
Surgery rates have not been assessed in this manuscript due to limited data on whether patients have been followed and recorded from their first surgery, and whether they had subsequent surgeries.
Furthermore, it should be noted that the JMDC database collects data from Diagnosis Procedure Combination (DPC) and non-DPC hospitals nationwide, and the given dataset does not allow for sufficiently accurate analyses by geographical regions and prefectures [20].
In conclusion, while BD and GIBD prevalence slightly increased in Japan between 2017 and 2021, incidence declined, which was particularly notable for confirmed GIBD cases. In parallel, the use of TNFαi biologics for BD and GIBD management increased over the same period in Japan. This change in BD treatment patterns, along with the Japanese diagnostic criteria adjustment in 2020, may have impacted the observed decrease in GIBD incidence. Further studies are needed to better understand the effectiveness of TNFαi biologics to treat GIBD as well as other BD subtypes, and to help achieve a more personalized treatment approach. These strategies may improve the availability of TNFαi biologics in Japan, potentially replacing the long-term use of GCs, which are often still administered as the initial therapeutic option for BD management.
Acknowledgements
This study was sponsored by Ferring Pharmaceuticals. Medical writing support for the development of this manuscript, under the direction of the authors, was provided by Ashfield MedComms GmbH, an Inizio company, and funded by Ferring Pharmaceuticals. Ferring Pharmaceuticals thanks Prospection (Japanese Analytics Team, Tokyo, Japan; https://www.prospectionhealthdata.com/) for the analysis of the JMDC data and critical review of this article.
Declarations
Conflict of interest
Tadakazu Hisamatsu received grant support from Mitsubishi Tanabe Pharma Corporation, EA pharma Co. Ltd., AbbVie GK, JIMRO Co. Ltd., Zeria Pharmaceutical Co. Ltd., Kyorin Pharmaceutical Co. Ltd., Nippon Kayaku Co. Ltd., Takeda Pharmaceutical Co. Ltd., Pfizer Inc., Mochida Pharmaceutical Co. Ltd., Boston Scientific Corporation, Kissei Pharmaceutical Co. Ltd; consulting fees from Mitsubishi Tanabe Pharma Corporation, EA pharma Co. Ltd., AbbVie GK, Janssen Pharmaceutical K.K., Pfizer Inc., Nichi-Iko Pharmaceutical Co., Ltd., Eli Lilly, Gilead Sciences, Bristol Myers Squibb; and lecture fees from Mitsubishi Tanabe Pharma Corporation, AbbVie GK, EA pharma Co. Ltd., Kyorin Pharmaceutical Co. Ltd., JIMRO Co., Janssen Pharmaceutical K.K., Mochida Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co. Ltd., Pfizer Inc. Kissei Pharmaceutical Co. Ltd. Makoto Naganuma received grants from Mitsubishi Tanabe Pharma Corporation, AbbVie GK, Kyorin Pharmaceutical Co., Ltd., Alfresa Pharma Corporation; and lecture fees from Tanabe Pharma Corporation, AbbVie GK, Takeda Pharmaceutical Co., Ltd., JIMRO Co., Ltd., Janssen Pharmaceutical K.K., Gilead Sciences, Inc. EA Pharma Co., Ltd., and Mochida Pharmaceutical Co., Ltd. Philippe Pinton is employed by Ferring Pharmaceuticals, is a Board of Directors member at PharmaBiome and owns stocks of Takeda Pharmaceutical Co., Ltd. Mitsuhiro Takeno received consulting fees, speaking fees, and research grants from AbbVie GK, Amgen K. K., Asahi Kasei, Astellas Pharma Inc., Nippon Boehringer-Ingelheim Co., Ltd., Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Eli Lilly Japan K. K., Mitsubishi Tanabe Pharma Corporation, Nippon Shinyaku, Novartis, Ono Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Taisyo Pharma, UBC Japan, and Viatris.
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