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Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis

PURPOSE: Immune checkpoint inhibitor (ICI) therapy is often suspended because of immune-related enterocolitis (irEC). We examined the effect of resumption of ICIs with or without concurrent selective immunosuppressive therapy (SIT) on rates of symptom recurrence and survival outcomes. METHODS: This...

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Autores principales: Badran, Yousef R, Zou, Fangwen, Durbin, Sienna M, Dutra, Barbara E, Abu-Sbeih, Hamzah, Thomas, Anusha S, Altan, Mehmet, Thompson, John A, Qiao, Wei, Leet, Donna E, Lai, Po-Ying, Horick, Nora K, Postow, Michael A, Faleck, David M, Wang, Yinghong, Dougan, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314704/
https://www.ncbi.nlm.nih.gov/pubmed/37349130
http://dx.doi.org/10.1136/jitc-2023-007195
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author Badran, Yousef R
Zou, Fangwen
Durbin, Sienna M
Dutra, Barbara E
Abu-Sbeih, Hamzah
Thomas, Anusha S
Altan, Mehmet
Thompson, John A
Qiao, Wei
Leet, Donna E
Lai, Po-Ying
Horick, Nora K
Postow, Michael A
Faleck, David M
Wang, Yinghong
Dougan, Michael
author_facet Badran, Yousef R
Zou, Fangwen
Durbin, Sienna M
Dutra, Barbara E
Abu-Sbeih, Hamzah
Thomas, Anusha S
Altan, Mehmet
Thompson, John A
Qiao, Wei
Leet, Donna E
Lai, Po-Ying
Horick, Nora K
Postow, Michael A
Faleck, David M
Wang, Yinghong
Dougan, Michael
author_sort Badran, Yousef R
collection PubMed
description PURPOSE: Immune checkpoint inhibitor (ICI) therapy is often suspended because of immune-related enterocolitis (irEC). We examined the effect of resumption of ICIs with or without concurrent selective immunosuppressive therapy (SIT) on rates of symptom recurrence and survival outcomes. METHODS: This retrospective, multicenter study examined patients who were treated with ICI and developed irEC requiring SIT (infliximab or vedolizumab) for initial symptom control or to facilitate steroid tapering between May 2015 and June 2020. After symptom resolution, patients were restarted either on ICI alone or on concurrent ICI and SIT at the discretion of the treating physicians. The associations between irEC recurrence and treatment group were assessed via univariate analyses and multivariate logistic regression. Cox proportional hazards model was used for survival analysis. RESULTS: Of the 138 included patients who required SIT for initial irEC symptom control, 61 (44.2%) patients resumed ICI without concurrent SIT (control group) and 77 (55.8%) patients resumed ICI therapy with concurrent SIT: 33 with infliximab and 44 with vedolizumab. After symptom resolution, patients in the control group were more commonly restarted on a different ICI regimen (65.6%) compared with those receiving SIT (31.2%) (p<0.001). The total number of ICI doses administered after irEC resolution and ICI resumption was similar in both groups (four to five doses). Recurrence of severe colitis or diarrhea after ICI resumption was seen in 34.4% of controls compared with 20.8% of patients receiving concurrent SIT. Concurrent SIT was associated with reduced risk of severe irEC recurrence after ICI resumption in a multivariate logistic regression model (OR 0.34; 95% CI 0.13 to 0.92; p=0.034). There was no difference in survival outcomes between patients in the control group and patients concurrently treated with SIT. CONCLUSION: After resolution of irEC symptoms, reinitiation of ICI with concurrent SIT is safe, reduces severe irEC recurrence, and has no negative impact on survival outcomes.
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spelling pubmed-103147042023-07-02 Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis Badran, Yousef R Zou, Fangwen Durbin, Sienna M Dutra, Barbara E Abu-Sbeih, Hamzah Thomas, Anusha S Altan, Mehmet Thompson, John A Qiao, Wei Leet, Donna E Lai, Po-Ying Horick, Nora K Postow, Michael A Faleck, David M Wang, Yinghong Dougan, Michael J Immunother Cancer Clinical/Translational Cancer Immunotherapy PURPOSE: Immune checkpoint inhibitor (ICI) therapy is often suspended because of immune-related enterocolitis (irEC). We examined the effect of resumption of ICIs with or without concurrent selective immunosuppressive therapy (SIT) on rates of symptom recurrence and survival outcomes. METHODS: This retrospective, multicenter study examined patients who were treated with ICI and developed irEC requiring SIT (infliximab or vedolizumab) for initial symptom control or to facilitate steroid tapering between May 2015 and June 2020. After symptom resolution, patients were restarted either on ICI alone or on concurrent ICI and SIT at the discretion of the treating physicians. The associations between irEC recurrence and treatment group were assessed via univariate analyses and multivariate logistic regression. Cox proportional hazards model was used for survival analysis. RESULTS: Of the 138 included patients who required SIT for initial irEC symptom control, 61 (44.2%) patients resumed ICI without concurrent SIT (control group) and 77 (55.8%) patients resumed ICI therapy with concurrent SIT: 33 with infliximab and 44 with vedolizumab. After symptom resolution, patients in the control group were more commonly restarted on a different ICI regimen (65.6%) compared with those receiving SIT (31.2%) (p<0.001). The total number of ICI doses administered after irEC resolution and ICI resumption was similar in both groups (four to five doses). Recurrence of severe colitis or diarrhea after ICI resumption was seen in 34.4% of controls compared with 20.8% of patients receiving concurrent SIT. Concurrent SIT was associated with reduced risk of severe irEC recurrence after ICI resumption in a multivariate logistic regression model (OR 0.34; 95% CI 0.13 to 0.92; p=0.034). There was no difference in survival outcomes between patients in the control group and patients concurrently treated with SIT. CONCLUSION: After resolution of irEC symptoms, reinitiation of ICI with concurrent SIT is safe, reduces severe irEC recurrence, and has no negative impact on survival outcomes. BMJ Publishing Group 2023-06-22 /pmc/articles/PMC10314704/ /pubmed/37349130 http://dx.doi.org/10.1136/jitc-2023-007195 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Clinical/Translational Cancer Immunotherapy
Badran, Yousef R
Zou, Fangwen
Durbin, Sienna M
Dutra, Barbara E
Abu-Sbeih, Hamzah
Thomas, Anusha S
Altan, Mehmet
Thompson, John A
Qiao, Wei
Leet, Donna E
Lai, Po-Ying
Horick, Nora K
Postow, Michael A
Faleck, David M
Wang, Yinghong
Dougan, Michael
Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis
title Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis
title_full Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis
title_fullStr Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis
title_full_unstemmed Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis
title_short Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis
title_sort concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis
topic Clinical/Translational Cancer Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314704/
https://www.ncbi.nlm.nih.gov/pubmed/37349130
http://dx.doi.org/10.1136/jitc-2023-007195
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