Sub-optimal Response to Anti-Tumor Necrosis Factor's in Inflammatory Bowel Disease in Emerging Markets

Takeda1,731 enrolled

Overview

The purpose of this study is to establish the incidence of sub-optimal response to anti-TNF therapy in UC and CD participants.

Participants with historical diagnosis of CD and UC who were naïve to anti-TNF therapy were observed in this retrospective study. The study will look to identify the local barriers in prescribing anti-TNF therapy, treatment patterns and indicators of sub-optimal response to anti-TNF therapy in UC and CD participants in real-world clinical practice in the EM countries, along with the associated incidence of sub-optimal response and impact on health care resource utilization (HCRU). The will enroll approximately 2000 participants. The study consists of two periods, eligibility period followed by a data abstraction period. During the eligibility period participants who had initiated first anti-TNF therapy during 01 March 2010 up to 01 March 2015 will be recruited and observed. Participants will be followed up for a period of minimum 2 years (other than death) and a maximum of 5 years from the date of first treatment of anti-TNF therapy for CD and UC (Index date). During the data abstraction period participants who have eligible medical charts will be identified and all retrospective data will be collected. This multi-center trial will be conducted in Argentina, China, Colombia, Mexico, Russia, Saudi Arabia, Singapore, South Korea, Taiwan and Turkey. The overall time to abstract data during the data extraction period from the web-based electronic data capture (EDC) system will be approximately 1 year from March 2017 to February 2018.

Study Type

OBSERVATIONAL

Enrollment

1,731

Conditions

Colitis, Ulcerative Crohn Disease Inflammatory Bowel Diseases

Interventions

Anti-TNF TherapyDRUG

Anti-TNF therapy.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Who are 18 years or older at Index Date and diagnosed with UC or CD. 2. Who were naive to anti-TNF therapy and received their first dose of any anti-TNF therapy (index date) for UC or CD within the Eligibility Period from 01 March 2010 through 01 March 2015. Exclusion Criteria: 1. Diagnosed with indeterminate/unspecified type of IBD. 2. Were part of an IBD-related clinical trial during the observational period should be excluded (that is, index date up to the date of chart abstraction). 3. Who received an anti-TNF therapy for any non-UC or non-CD conditions (example, rheumatoid arthritis, ankylosing spondylitis, psoriasis, or cancer). 4. Who received an anti-TNF/biologic therapy at any point that was administered outside of the labelled dosing regimen (example, episodic use of anti-TNF therapy). 5. With UC who had a total colectomy prior to their first anti-TNF therapy. 6. Charts not available.

Locations (76)

Outcomes

Primary Outcomes

Incidence Rate of Sub-optimal Response in UC and CD Participants

Incidence rate will be calculated as the number of events divided by the total person time at risk, for participants under anti-TNF therapy.

Time frame: 5 years

Treatment Patterns in UC and CD Participants

Time frame: 5 years

Number of Participants With Each Type of Anti-TNF Therapy

Time frame: 5 years

Duration of Treatment

Time frame: 5 years

Number of Participants With Response to Treatment

Number of participants with response to treatment will be assessed.

Time frame: 5 years

Treatment Pattern Results Stratified by Anti-TNF Response Group and by UC or CD Diagnosis

Treatment patterns results were as per the Anti-TNF therapy response from UC and CD participants.

Time frame: 5 years

Time-to-switch

The time to switch at which the participant switched to another anti-TNF therapy will be evaluated.

Time frame: 5 years

Time-to-first Indicator of Sub-optimal Therapy

Time-to-first indicator of sub-optimal therapy was defined as the occurrence of dose escalation, therapy augmentation, therapy switch, therapy discontinuation, hospitalization, or surgery of participant, which ever occurred first.

Time frame: 5 years

Secondary Outcomes

Data from ClinicalTrials.gov

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Hospital Italiano

Ciudad Autonoma Buenos Aires, Buenos Aires, Argentina

Hospital Italiano de La Plata

La Plata, Buenos Aires, Argentina

Hospital Aleman

Ciudad Autonoma Buenos Aires, Argentina

Hospital Britanico de Buenos Aires

Ciudad Autonoma Buenos Aires, Argentina

Hospital Privado Centro Medico de Cordoba

Córdoba, Argentina

Peking Union Medical College Hospital

Beijing, Beijing Municipality, China

The Sixth Affiliated Hospital of Sun Yat-Sen University

Guangzhou, Guangdong, China

The Affiliated Drum Tower Hospital of Nanjing University

Nanjing, Jiangsu, China

First Affiliated Hospital of Dalian Medical University

Dalian, Liaoning, China

Ruijin Hospital, Shanghai Jiaotong Uni. School of Med.

Huangpu, Shanghai Municipality, China

...and 66 more locations

Number of Participants With CD Achieving Clinical Response Based on Harvey Bradshaw Index (HBI)

Clinical response is defined as a decrease in HBI score of greater than or equal to (\>=) 3 points from baseline. HBI score is used to measure the disease activity of CD. It consists of clinical parameters: abdominal pain (0-3, higher score means more severe pain), number of liquid stools per day, abdominal mass (0-3, where higher score means presence of swelling in the abdomen), and complications (score 1 per item). Total score is the sum of individual parameters. The score ranges from a minimum score of 0 to no pre-specified maximum score as it depends on the number of liquid stools, where higher scores indicating more severe disease.

Time frame: Baseline up to 5 years

Number of Participants With UC Achieving Clinical Response Based on Mayo Scores

Clinical response is defined as a decrease in the partial Mayo Score of at least 2 points and \>=25% from baseline, with an accompanying decrease in rectal bleeding subscore of \>=1 point from baseline or absolute rectal bleeding subscore of less than or equal to (\<=) 1 point. Mayo score is an instrument designed to measure disease activity of UC. It consists of 3 subscores: stool frequency, rectal bleeding, and physician global assessment of disease severity, each graded from 0 to 3 with higher scores indicating more severe disease. These scores are summed to give a total score range of 0 to 9; where higher scores indicating more severe disease.

Time frame: Baseline up to 5 years

Number of Participants with Inflammatory Bowel Disease (IBD) Related Surgeries and Hospitalisation

IBD-related surgeries and hospitalisation will be conducted in the two years prior to index anti-TNF therapy in UC or CD participants.

Time frame: 2 years prior to index anti-TNF therapy

Number of Participants with Co-morbidities

Time frame: Baseline

Number of Participants with Predictors of Sub-optimal Therapy in UC or CD Participants

The predictors of sub-optimal response will be assessed through multivariate analysis using logistic regression or other appropriate statistical methods. Multivariate analyses may be conducted to derive predictors of sub-optimal response to anti-TNF therapy globally and individually.

Time frame: Baseline up to 5 years

Health Care Resources Utilisation (HCRU)

HCRU will be calculated for physician clinic visits, emergency department visits, IBD-related surgeries, invasive procedures, imaging, and in-participant admissions related to UC or CD, or related complications as available in the medical record and captured in the electronic case report form (eCRF).

Time frame: Baseline up to 7 years

Physician Survey Questionnaire

The physician survey questionnaire will include questions on local accessibility to infusion centres, potential restrictions of prescription, potential local difficulties for drug access (example, reimbursement process, economic burden), and other reasons for participants compliant with the local label to not receive anti-TNF therapy.

Time frame: Baseline