Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/35621
Title: Immunomodulator use does not prevent first loss of response to anti-tumour necrosis factor alpha therapy in inflammatory bowel disease: long-term outcomes in a real-world cohort.
Authors: Crantock L.R.F.;Sorrell C.;Rusli F.;Dev A. ;Moore G.T.;Pianko S. ;Ratnam D.T.;Varma P.;Rajadurai A.S.;Holt D.Q.;Devonshire D.A.;Desmond C.P.;Swan M.P. ;Nathan D.;Shelton E.T.;Prideaux L.
Institution: (Varma, Rajadurai, Holt, Devonshire, Desmond, Swan, Nathan, Shelton, Prideaux, Sorrell, Rusli, Crantock, Dev, Ratnam, Pianko, Moore) Department of Gastroenterology and Hepatology, Monash Medical Centre, Melbourne, VIC, Australia (Holt, Moore) School of Clinical Sciences, Monash University, Melbourne, VIC, Australia
Issue Date: 21-Jun-2019
Copyright year: 2019
Publisher: Blackwell Publishing
Place of publication: Australia
Publication information: Internal Medicine Journal. 49 (6) (pp 753-760), 2019. Date of Publication: June 2019.
Journal: Internal Medicine Journal
Abstract: Background: Recent prospective studies suggest combination therapy with immunomodulators improves efficacy, but long-term data is limited. Aim(s): To assess whether anti-tumour necrosis factor alpha (anti-TNF) monotherapy was associated with earlier loss of response (LOR) than combination therapy in a real-world cohort with long-term follow up. Method(s): A retrospective audit was conducted of inflammatory bowel disease patients receiving anti-TNF therapy in a tertiary centre and specialist private practices. All patients with accurate data for anti-TNF commencement and adequate correspondence to determine end-points were included. Outcomes measured included time to first LOR, causes and biochemical parameters. Result(s): Two hundred and twenty-four patients were identified; 139 (62.1%) on combination therapy and 85 (37.9%) on monotherapy. Forty-five percent of patients had LOR during follow up until a maximum of 8.5 years; 59.4% on combination therapy and 40.6% on monotherapy (P = 0.533). The median time to LOR was not different between groups; 1069 days for combination therapy and 1489 days for monotherapy (P = 0.533). There was no difference in time to LOR between patients treated with different combination regimens or different anti-TNF agents. Conclusion(s): In this large cohort of patients in a real-world setting, patients treated with anti-TNF monotherapy had similar rates of LOR as patients on anti-TNF combination therapy, at both short- and long-term follow up.Copyright © 2018 Royal Australasian College of Physicians
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/imj.14150
PubMed URL: 30381884 [http://www.ncbi.nlm.nih.gov/pubmed/?term=30381884]
ISSN: 1444-0903
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/35621
Type: Article
Subjects: drug withdrawal
female
follow up
human
infection/si [Side Effect]
*inflammatory bowel disease/dt [Drug Therapy]
long term care
major clinical study
male
medical specialist
melanoma/si [Side Effect]
monotherapy
mycoplasmosis/si [Side Effect]
osteomyelitis/si [Side Effect]
outcome assessment
perianal abscess/si [Side Effect]
pertussis/si [Side Effect]
priority journal
private practice
recurrent infection/si [Side Effect]
retina disease/si [Side Effect]
retrospective study
Clostridium infection/si [Side Effect]
combination drug therapy
controlled study
drug hypersensitivity/si [Side Effect]
*tumor necrosis factor inhibitor/ae [Adverse Drug Reaction]
*tumor necrosis factor inhibitor/cm [Drug Comparison]
*tumor necrosis factor inhibitor/dt [Drug Therapy]
adolescent
adult
alopecia areata/si [Side Effect]
article
bacterial infection/si [Side Effect]
clinical audit
cohort analysis
tertiary care center
treatment duration
treatment outcome
*treatment response
*immunomodulating agent/ae [Adverse Drug Reaction]
*immunomodulating agent/cm [Drug Comparison]
*immunomodulating agent/dt [Drug Therapy]
drug hypersensitivity / side effect
adolescent
adult
alopecia areata / side effect
Article
bacterial infection / side effect
clinical audit
Clostridium infection / side effect
cohort analysis
combination drug therapy
controlled study
drug withdrawal
female
follow up
human
infection / side effect
*inflammatory bowel disease / *drug therapy
long term care
major clinical study
male
medical specialist
melanoma / side effect
monotherapy
mycoplasmosis / side effect
osteomyelitis / side effect
outcome assessment
perianal abscess / side effect
pertussis / side effect
priority journal
private practice
recurrent infection / side effect
retina disease / side effect
retrospective study
tertiary care center
treatment duration
treatment outcome
*treatment response
Type of Clinical Study or Trial: Observational study (cohort, case-control, cross sectional or survey)
Appears in Collections:Articles

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