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©The Author(s) 2024.
World J Gastroenterol. Jun 14, 2024; 30(22): 2902-2919
Published online Jun 14, 2024. doi: 10.3748/wjg.v30.i22.2902
Published online Jun 14, 2024. doi: 10.3748/wjg.v30.i22.2902
Ref. | Number | Disease | PNR and/or SLOR | Study design | Intervention | Follow-up | Outcome | Result |
Trials: Vedolizumab dose escalation | ||||||||
Loftus et al[66] | 32 | UC | LOR | Single-arm open label-multicentre | 4 weekly 300 mg | 28 weeks | Clinical response/clinical remission | 53.1% (19% with response prior to escalation)/25.0% (6% in remission prior) |
Vermeire et al[67] | 57 | Crohn’s | LOR | Single-arm open label-multicentre | 4 weekly 300 mg | 28 weeks | Clinical Response/Clinical Remission | 54.4% (39% with response prior to escalation)/22.8% (4% in remission prior) |
Vaughn et al[68] | 58 | Crohn’s or UC | LOR | Retrospective cohort study-multicentre | 4-7 weekly 300 mg | 15 weeks | Clinical Response | 62.0% |
Gouynou et al[69] | 23 | Crohn’s or UC | PNR/LOR | Retrospective cohort study-single centre | NS-increased frequency | 9 months | Clinical response | 52.2% |
Outtier et al[70] | 59 | Crohn’s or UC | LOR | Prospective observational study-multicentre | 4 weekly 300 mg | 8 weeks | Clinical response | 54.2% |
Kolehmainen et al[71] | 36 | Crohn’s or UC | PNR/LOR | Retrospective cohort study-single centre | NS-increased frequency | 12 months | Clinical response | 33.3% |
Perry et al[23] | 24 | UC | PNR/Partial Responder | Retrospective cohort study-single centre | 4 weekly 300 mg | 51 weeks | Clinical response/corticosteroid free remission | 41.7%/41.7% |
Christensen et al[72] | 43 | Crohn’s or UC | NS | Prospective cohort study-single centre | 4 or 6 weekly 300 mg | 26 weeks | Clinical response/clinical remission | 58.1%/55.8% |
Dreesen et al[74] | 16 | Crohn’s or UC | NS | Retrospective cohort study-single centre | 4 weekly 300 mg | 14 weeks (UC), 22 weeks (Crohn’s) | Clinical response | 56.3% |
Kopylov et al[73] | 48 | Crohn’s or UC | NS | Retrospective cohort study-multicentre | 4 weekly 300 mg | 52 weeks | Clinical response | 62.5% |
Williet et al[75] | 15 | Crohn’s or UC | PNR | Prospective cohort study-single centre | 4 weekly 300 mg | 36 weeks | Clinical response | 53.8% |
Attauabi et al[76] | 37 | Crohn’s or UC | LOR | Retrospective cohort study-2 centre | 4-7 weekly 300 mg | < 70 weeks | Clinical remission | 62.2% |
Jairath et al[77] | 55 | UC | PNR | Open label multicentre RCT | 4 weekly 300mg or 600 mg | 30 weeks | Clinical response/clinical remission | 30.9/9.1% |
Trials: Ustekinumab frequency | ||||||||
Dalal et al[41] | 75 | Crohn’s | LOR | Retrospective cohort study-single centre | 4 or 6 weekly 90 mg | 12 months | Corticosteroid free clinical remission | 54.7% |
Derikx et al[48] | 47 | Crohn’s | NS | Retrospective cohort study-single centre | 4 or 6 weekly 90 mg | 8.9 months | Corticosteroid free remission | 29.6% |
Bundschuh et al[98] | 27 | Crohn’s | LOR | Retrospective cohort study | 4 or 6 weekly 90 mg | NS | Clinical response | 54.5% |
Haider et al[100] | 15 | Crohn’s | PNR | Retrospective cohort study-single centre | 4 weekly 90 mg | 78 weeks | Clinical response/clinical remission | 46.6%/33.3% |
Fumery et al[101] | 100 | Crohn’s | Partial Response/LOR | Retrospective cohort study-single centre | 4 weekly 90 mg | 2.4 months | Clinical response/clinical remission | 61%/31% |
Ollech et al[102] | 51 | Crohn’s | NS | Retrospective cohort study-single centre | 4 weekly 90 mg | 5.9 months | Clinical remission | 27.5% |
Dalal et al[96] | 157 (Crohn’s: 117, UC: 40) | Crohn’s or UC | Partial Response/LOR | Retrospective cohort study-single centre | 4 or 6 weekly 90 mg | 12 months | Steroid free clinical remission | Crohn’s 57.3%/UC 52.5% |
Rowbotham et al[107] | 24 | UC | NS | Randomised-withdrawal maintenance study | 8 weekly 90 mg | 16 weeks | Clinical remission | 58.3% |
Trials: Ustekinumab reinduction | ||||||||
Sedano et al[109] | 15 | Crohn’s | Partial Response/LOR | Retrospective cohort study-single centre | IV reinduction | 14.9 weeks | Clinical response/clinical remission | 66.7%/53.3% |
Heron et al[110] | 65 | Crohn’s | Partial Response/LOR | Retrospective cohort study - multicentre | IV reinduction | 14 weeks | Clinical Remission with either biochemical and endoscopic response or remission | 31.0% |
Bermejo et al[111] | 43 | Crohn’s | LOR | Retrospective cohort study-multicentre | IV re-induction | 16 weeks | Clinical response/clinical remission | 52.8%/43.3% |
Ten Bokkel et al[112] | 29 | Crohn’s | LOR | Prospective cohort study-multicentre | IV re-induction | 52 weeks | Clinical remission | 44.8% |
Trials: Ustekinumab increased frequency and/or reinduction | ||||||||
Cohen et al[99] | 68 | Crohn’s | PNR/Partial Response | Retrospective cohort study-single centre | IV induction + 4 or 6 weekly 90 mg | 3-6 months | Clinical response/clinical remission | 79.4%/30.9% |
Yao et al[114] | 128 | Crohn’s | Partial Response/LOR | Retrospective cohort study-single centre | 4 weekly 90 mg +/- IV Re-induction | 3 months | Clinical remission | 62.9% Shortening/69.6% re-induction |
Hudson et al[113] | 18 | Crohn’s | SLOR | Retrospective case series-single centre | IV re-induction +/- 4 or 6 weekly 90 mg | 4-8 weeks | Clinical remission or response | 83.3% |
Ramaswamy et al[106] | 31 | Crohn’s | Partial response/LOR | Retrospective cohort study-single centre | 4 weekly 90 mg +/- IV re-induction | 12 weeks | Clinical response | 64.5% |
Chaparro et al[40] | 60 | Crohn’s | PNR/LOR | Retrospective cohort study-multicentre | 4 weekly 90 mg /IV re-induction | NS | Clinical remission | 78.3% |
Ma et al[115] | 24 | Crohn’s | LOR | Retrospective cohort study-multicentre | 4 or 6 weekly 90 mg +/- IV reinduction | NS | Clinical response | 54.2% |
Young et al[97] | 21 | Crohn’s | PNR/LOR/partial response | Retrospective cohort study-single centre | 4 or 6 weekly 90 mg +/- IV induction | 177 days | Clinical response | 52.4% |
Johnson et al[103] | 229 | Crohn’s | PNR/LOR | Retrospective cohort study-multicentre | 4 or 6 weekly 90 mg + IV reinduction/IV reinduction | NS | Clinical response | 45.9% |
Olmedo et al[104] | 91 | Crohn’s | PNR/LOR | Retrospective cohort study-multicentre | 4 or 6 weekly 90 mg + IV reinduction | 16 weeks | Steroid free clinical response/Steroid free clinical remission | 62.6%/25.3% |
Kopylov et al[105] | 142 | Crohn’s | NS | Retrospective cohort study-multicentre | 4 or 6 weekly 90 mg +/- IV induction | 16 weeks | Clinical response/clinical remission | 51.4%/38.7% |
Trials: Tofacitinib dose escalation | ||||||||
Ma et al[51] | 71 | UC | LOR | Prospective cohort study-multicentre | 10 mg BD | NS | Clinical response | 54.9% |
Honap et al[52] | 19 | UC | LOR | Retrospective cohort study-multicentre | 10 mg BD | NS | Clinical response | 47.4% |
Sandborn et al[150] | 57 | UC | LOR | Prospective cohort study-multicentre | 10 mg BD | 12 months | Clinical response/clinical remission | 64.9%/49.1% |
Trials: Upadacitinib dose escalation | ||||||||
Sandborn et al[151] | 60 | Crohn’s | NS (inadequate response) | Phase II placebo controlled RCT | 12 mg BD/24 mg BD IR | 52 weeks | Clinical remissions | 15% 12 mg BD/24 mg BD 39% |
Panaccione et al[153] | 190 | UC | LOR/inadequate response | Prospective cohort study | 30 mg ER daily | 48 weeks | Clinical remission | 27.9% |
- Citation: Vootukuru N, Vasudevan A. Approach to loss of response to advanced therapies in inflammatory bowel disease. World J Gastroenterol 2024; 30(22): 2902-2919
- URL: https://www.wjgnet.com/1007-9327/full/v30/i22/2902.htm
- DOI: https://dx.doi.org/10.3748/wjg.v30.i22.2902