Comparative Persistence of Non-tumor Necrosis Factor (TNF) vs. TNF Antagonists for Post-operative Prophylaxis in Crohn’s Disease (CD)
Background The comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn’s disease (CD) is uncertain. Drug persistence may serve as a real-world proxy for tolerability and effectiveness. We evaluated the comparative persistence of non-TNF and TNF antagonists...
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Published in | Digestive diseases and sciences Vol. 69; no. 1; pp. 235 - 245 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.01.2024
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0163-2116 1573-2568 1573-2568 |
DOI | 10.1007/s10620-023-08192-w |
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Abstract | Background
The comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn’s disease (CD) is uncertain. Drug persistence may serve as a real-world proxy for tolerability and effectiveness. We evaluated the comparative persistence of non-TNF and TNF antagonists for post-operative prophylaxis and their comparative effectiveness for preventing early endoscopic post-operative recurrence (POR).
Methods
We conducted a single-center, retrospective study of surgically naïve CD subjects undergoing ileocecal or small bowel resection between 1/1/2000 and 12/31/2021 and prescribed a biologic for post-operative prophylaxis. We compared the risk of prophylaxis failure (requiring recurrent surgery or discontinuation of therapy due to persistent POR despite optimized drug level or dose escalation, immunogenicity, and/or adverse event) and early endoscopic POR (Rutgeert’s score ≥ i2 within 15 months postoperatively) between non-TNF and TNF antagonist prophylaxis using Cox proportional hazard and logistic regression, respectively, adjusting for demographic and disease characteristics.
Results
The study included 291 subjects (81% TNF antagonists). After multivariable adjustment, non-TNF antagonist prophylaxis was associated with a significantly lower risk of prophylaxis failure than TNF antagonists (hazard ratio 0.26; 95% confidence interval (CI) [0.13–0.53]). Prophylaxis with non-TNF and TNF antagonists had similar risk of early endoscopic POR (odds ratio 0.66; 95% CI [0.32–1.36]). Stratifying the non-TNF antagonists by anti-integrin and anti-IL12/23 yielded similar results.
Conclusion
In a cohort of surgically naïve CD subjects prescribed a biologic for post-operative prophylaxis, non-TNF antagonists had greater persistence than TNF antagonists with similar risk for early endoscopic POR. If confirmed by large, prospective studies, these findings can inform post-operative management strategies in CD. |
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AbstractList | The comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn's disease (CD) is uncertain. Drug persistence may serve as a real-world proxy for tolerability and effectiveness. We evaluated the comparative persistence of non-TNF and TNF antagonists for post-operative prophylaxis and their comparative effectiveness for preventing early endoscopic post-operative recurrence (POR).BACKGROUNDThe comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn's disease (CD) is uncertain. Drug persistence may serve as a real-world proxy for tolerability and effectiveness. We evaluated the comparative persistence of non-TNF and TNF antagonists for post-operative prophylaxis and their comparative effectiveness for preventing early endoscopic post-operative recurrence (POR).We conducted a single-center, retrospective study of surgically naïve CD subjects undergoing ileocecal or small bowel resection between 1/1/2000 and 12/31/2021 and prescribed a biologic for post-operative prophylaxis. We compared the risk of prophylaxis failure (requiring recurrent surgery or discontinuation of therapy due to persistent POR despite optimized drug level or dose escalation, immunogenicity, and/or adverse event) and early endoscopic POR (Rutgeert's score ≥ i2 within 15 months postoperatively) between non-TNF and TNF antagonist prophylaxis using Cox proportional hazard and logistic regression, respectively, adjusting for demographic and disease characteristics.METHODSWe conducted a single-center, retrospective study of surgically naïve CD subjects undergoing ileocecal or small bowel resection between 1/1/2000 and 12/31/2021 and prescribed a biologic for post-operative prophylaxis. We compared the risk of prophylaxis failure (requiring recurrent surgery or discontinuation of therapy due to persistent POR despite optimized drug level or dose escalation, immunogenicity, and/or adverse event) and early endoscopic POR (Rutgeert's score ≥ i2 within 15 months postoperatively) between non-TNF and TNF antagonist prophylaxis using Cox proportional hazard and logistic regression, respectively, adjusting for demographic and disease characteristics.The study included 291 subjects (81% TNF antagonists). After multivariable adjustment, non-TNF antagonist prophylaxis was associated with a significantly lower risk of prophylaxis failure than TNF antagonists (hazard ratio 0.26; 95% confidence interval (CI) [0.13-0.53]). Prophylaxis with non-TNF and TNF antagonists had similar risk of early endoscopic POR (odds ratio 0.66; 95% CI [0.32-1.36]). Stratifying the non-TNF antagonists by anti-integrin and anti-IL12/23 yielded similar results.RESULTSThe study included 291 subjects (81% TNF antagonists). After multivariable adjustment, non-TNF antagonist prophylaxis was associated with a significantly lower risk of prophylaxis failure than TNF antagonists (hazard ratio 0.26; 95% confidence interval (CI) [0.13-0.53]). Prophylaxis with non-TNF and TNF antagonists had similar risk of early endoscopic POR (odds ratio 0.66; 95% CI [0.32-1.36]). Stratifying the non-TNF antagonists by anti-integrin and anti-IL12/23 yielded similar results.In a cohort of surgically naïve CD subjects prescribed a biologic for post-operative prophylaxis, non-TNF antagonists had greater persistence than TNF antagonists with similar risk for early endoscopic POR. If confirmed by large, prospective studies, these findings can inform post-operative management strategies in CD.CONCLUSIONIn a cohort of surgically naïve CD subjects prescribed a biologic for post-operative prophylaxis, non-TNF antagonists had greater persistence than TNF antagonists with similar risk for early endoscopic POR. If confirmed by large, prospective studies, these findings can inform post-operative management strategies in CD. The comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn's disease (CD) is uncertain. Drug persistence may serve as a real-world proxy for tolerability and effectiveness. We evaluated the comparative persistence of non-TNF and TNF antagonists for post-operative prophylaxis and their comparative effectiveness for preventing early endoscopic post-operative recurrence (POR). We conducted a single-center, retrospective study of surgically naïve CD subjects undergoing ileocecal or small bowel resection between 1/1/2000 and 12/31/2021 and prescribed a biologic for post-operative prophylaxis. We compared the risk of prophylaxis failure (requiring recurrent surgery or discontinuation of therapy due to persistent POR despite optimized drug level or dose escalation, immunogenicity, and/or adverse event) and early endoscopic POR (Rutgeert's score ≥ i2 within 15 months postoperatively) between non-TNF and TNF antagonist prophylaxis using Cox proportional hazard and logistic regression, respectively, adjusting for demographic and disease characteristics. The study included 291 subjects (81% TNF antagonists). After multivariable adjustment, non-TNF antagonist prophylaxis was associated with a significantly lower risk of prophylaxis failure than TNF antagonists (hazard ratio 0.26; 95% confidence interval (CI) [0.13-0.53]). Prophylaxis with non-TNF and TNF antagonists had similar risk of early endoscopic POR (odds ratio 0.66; 95% CI [0.32-1.36]). Stratifying the non-TNF antagonists by anti-integrin and anti-IL12/23 yielded similar results. In a cohort of surgically naïve CD subjects prescribed a biologic for post-operative prophylaxis, non-TNF antagonists had greater persistence than TNF antagonists with similar risk for early endoscopic POR. If confirmed by large, prospective studies, these findings can inform post-operative management strategies in CD. BackgroundThe comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn’s disease (CD) is uncertain. Drug persistence may serve as a real-world proxy for tolerability and effectiveness. We evaluated the comparative persistence of non-TNF and TNF antagonists for post-operative prophylaxis and their comparative effectiveness for preventing early endoscopic post-operative recurrence (POR).MethodsWe conducted a single-center, retrospective study of surgically naïve CD subjects undergoing ileocecal or small bowel resection between 1/1/2000 and 12/31/2021 and prescribed a biologic for post-operative prophylaxis. We compared the risk of prophylaxis failure (requiring recurrent surgery or discontinuation of therapy due to persistent POR despite optimized drug level or dose escalation, immunogenicity, and/or adverse event) and early endoscopic POR (Rutgeert’s score ≥ i2 within 15 months postoperatively) between non-TNF and TNF antagonist prophylaxis using Cox proportional hazard and logistic regression, respectively, adjusting for demographic and disease characteristics.ResultsThe study included 291 subjects (81% TNF antagonists). After multivariable adjustment, non-TNF antagonist prophylaxis was associated with a significantly lower risk of prophylaxis failure than TNF antagonists (hazard ratio 0.26; 95% confidence interval (CI) [0.13–0.53]). Prophylaxis with non-TNF and TNF antagonists had similar risk of early endoscopic POR (odds ratio 0.66; 95% CI [0.32–1.36]). Stratifying the non-TNF antagonists by anti-integrin and anti-IL12/23 yielded similar results.ConclusionIn a cohort of surgically naïve CD subjects prescribed a biologic for post-operative prophylaxis, non-TNF antagonists had greater persistence than TNF antagonists with similar risk for early endoscopic POR. If confirmed by large, prospective studies, these findings can inform post-operative management strategies in CD. Background The comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn’s disease (CD) is uncertain. Drug persistence may serve as a real-world proxy for tolerability and effectiveness. We evaluated the comparative persistence of non-TNF and TNF antagonists for post-operative prophylaxis and their comparative effectiveness for preventing early endoscopic post-operative recurrence (POR). Methods We conducted a single-center, retrospective study of surgically naïve CD subjects undergoing ileocecal or small bowel resection between 1/1/2000 and 12/31/2021 and prescribed a biologic for post-operative prophylaxis. We compared the risk of prophylaxis failure (requiring recurrent surgery or discontinuation of therapy due to persistent POR despite optimized drug level or dose escalation, immunogenicity, and/or adverse event) and early endoscopic POR (Rutgeert’s score ≥ i2 within 15 months postoperatively) between non-TNF and TNF antagonist prophylaxis using Cox proportional hazard and logistic regression, respectively, adjusting for demographic and disease characteristics. Results The study included 291 subjects (81% TNF antagonists). After multivariable adjustment, non-TNF antagonist prophylaxis was associated with a significantly lower risk of prophylaxis failure than TNF antagonists (hazard ratio 0.26; 95% confidence interval (CI) [0.13–0.53]). Prophylaxis with non-TNF and TNF antagonists had similar risk of early endoscopic POR (odds ratio 0.66; 95% CI [0.32–1.36]). Stratifying the non-TNF antagonists by anti-integrin and anti-IL12/23 yielded similar results. Conclusion In a cohort of surgically naïve CD subjects prescribed a biologic for post-operative prophylaxis, non-TNF antagonists had greater persistence than TNF antagonists with similar risk for early endoscopic POR. If confirmed by large, prospective studies, these findings can inform post-operative management strategies in CD. |
Author | Bonthala, Niru Syal, Gaurav Li, Dalin Yarur, Andres Fleshner, Phillip Dube, Shishir Haritunians, Talin Vasiliauskas, Eric Targan, Stephan Yang, Shaohong McGovern, Dermot P. B. Gu, Phillip Melmed, Gil Y. Lee, YooJin Ziring, David Rabizadeh, Shervin |
Author_xml | – sequence: 1 givenname: Phillip orcidid: 0000-0003-4819-8979 surname: Gu fullname: Gu, Phillip email: phillip.gu@cshs.org organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 2 givenname: Shishir surname: Dube fullname: Dube, Shishir organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 3 givenname: YooJin surname: Lee fullname: Lee, YooJin organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 4 givenname: Shaohong surname: Yang fullname: Yang, Shaohong organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 5 givenname: Dalin surname: Li fullname: Li, Dalin organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 6 givenname: Talin surname: Haritunians fullname: Haritunians, Talin organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 7 givenname: Eric surname: Vasiliauskas fullname: Vasiliauskas, Eric organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 8 givenname: Niru surname: Bonthala fullname: Bonthala, Niru organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 9 givenname: Gaurav surname: Syal fullname: Syal, Gaurav organization: Division of Gastroenterology, Department of Medicine, UC San Diego – sequence: 10 givenname: Andres surname: Yarur fullname: Yarur, Andres organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 11 givenname: David surname: Ziring fullname: Ziring, David organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 12 givenname: Stephan surname: Targan fullname: Targan, Stephan organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 13 givenname: Shervin surname: Rabizadeh fullname: Rabizadeh, Shervin organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 14 givenname: Gil Y. surname: Melmed fullname: Melmed, Gil Y. organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 15 givenname: Phillip surname: Fleshner fullname: Fleshner, Phillip organization: F. Widjaja Inflammatory Bowel Disease Institute – sequence: 16 givenname: Dermot P. B. surname: McGovern fullname: McGovern, Dermot P. B. organization: F. Widjaja Inflammatory Bowel Disease Institute |
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Keywords | Post-operative prophylaxis Comparative effectiveness Post-operative recurrence Drug persistence Crohn’s disease |
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The comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn’s disease (CD) is uncertain. Drug... The comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn's disease (CD) is uncertain. Drug persistence may serve... BackgroundThe comparative safety and effectiveness of available biologics for post-operative prophylaxis in Crohn’s disease (CD) is uncertain. Drug persistence... |
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SubjectTerms | Biochemistry Crohn Disease - drug therapy Crohn Disease - prevention & control Crohn Disease - surgery Crohn's disease Disease prevention Endoscopy Gastroenterology Hepatology Humans Medicine Medicine & Public Health Necrosis Oncology Original Original Article Prospective Studies Retrospective Studies Transplant Surgery Tumor Necrosis Factor Inhibitors - adverse effects Tumor Necrosis Factor-alpha Tumor necrosis factor-TNF |
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Title | Comparative Persistence of Non-tumor Necrosis Factor (TNF) vs. TNF Antagonists for Post-operative Prophylaxis in Crohn’s Disease (CD) |
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