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Brunet, E. Combined Biological Therapy for Refractory Inflammatory Bowel Disease. Encyclopedia. Available online: https://encyclopedia.pub/entry/20880 (accessed on 16 November 2024).
Brunet E. Combined Biological Therapy for Refractory Inflammatory Bowel Disease. Encyclopedia. Available at: https://encyclopedia.pub/entry/20880. Accessed November 16, 2024.
Brunet, Eduard. "Combined Biological Therapy for Refractory Inflammatory Bowel Disease" Encyclopedia, https://encyclopedia.pub/entry/20880 (accessed November 16, 2024).
Brunet, E. (2022, March 22). Combined Biological Therapy for Refractory Inflammatory Bowel Disease. In Encyclopedia. https://encyclopedia.pub/entry/20880
Brunet, Eduard. "Combined Biological Therapy for Refractory Inflammatory Bowel Disease." Encyclopedia. Web. 22 March, 2022.
Combined Biological Therapy for Refractory Inflammatory Bowel Disease
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This entry is adapted from the peer-reviewed paper 10.3390/jcm11041076

Current medical treatment for inflammatory bowel disease (IBD) does not achieve 100% response rates, and a subset of refractory and severely ill patients have persistent active disease after being treated with all possible drug alternatives. Ustekinumab plus vedolizumab and vedolizumab plus anti-TNF were the most used biological therapies (CoT) for Crohn’s disease. For ulcerative colitis, the most used CoTs were vedolizumab plus anti-TNF and vedolizumab plus tofacitinib. 

inflammatory bowel diseases biologic treatment combination

1. Introduction

Currently, there is a reasonable number of useful therapies for IBD. The treatment armamentarium includes small molecules and biological treatments. Small molecules include classical drugs such as mesalazine, corticosteroids, and immunosuppressant treatments; this latter group includes thiopurines, methotrexate for Crohn’s disease (CD), and tofacitinib for ulcerative colitis (UC). Regarding biological treatments, anti-TNF drugs, vedolizumab, and ustekinumab are currently widely used [1][2].
These drugs are mostly used sequentially. Thus, if a drug is ineffective in controlling IBD symptoms, that drug is withdrawn and replaced by another (for example, in patients who have active disease despite receiving an anti-TNF drug, treatment with the anti-TNF drug would be stopped and the patient would begin treatment with an alternative biological drug). The only exception is the combination of an anti-TNF plus azathioprine, which has been widely used in clinical practice since the 2010 SONIC trial showed that this combination achieved higher remission and mucosal healing rates than monotherapy without a clear increase in adverse events [3].
Used individually, IBD therapies reach a maximum clinical remission rate of approximately 40–60% [4]. Therefore, current medical treatment for IBD does not achieve 100% response rates, and a subset of refractory and severely ill patients have persistent active disease after being treated with all the possible drug alternatives. These patients often require aggressive rescue therapies such as major surgery or bone marrow auto-transplant in CD, or proctocolectomy in UC [5][6].
As these rescue treatments have significant risks and may have a negative impact on quality of life, the combination of two biological therapies (CoT) seems a reasonable alternative. In fact, CoT has been increasingly tested in very difficult cases and in two clearly different settings: in patients with uncontrolled IBD, and in patients with controlled IBD but extraintestinal manifestations that did not respond to a single biological therapy [7]. The safety and efficacy of CoT have mostly been reported as case reports or short series [4].

2. Global Efficacy and Safety of CoT

Ribaldone et al. reported seven studies (18 patients) with a combination of TNF inhibitors and vedolizumab as well as vedolizumab and ustekinumab. Clinical improvement was seen in all patients, and endoscopic improvement was reported in 93% of patients. No safety concerns were identified [8].
In 2021, Gold et al. reported a review pooling data from 209 CoTs. They included retrospective studies, case reports, and case series. This review suggested that dual biologic therapy may be effective at inducing remission in patients with refractory luminal symptoms and/or extraintestinal manifestations. They reported an efficacy ranging from 67% to 80%. No severe adverse events were described [7].

3. Usefulness and Safety of Biologic Combinations

Figure 1 shows the pooled rates of clinical response, clinical remission endoscopic response, endoscopic remission, and adverse event rates for the most used CoTs.
Jcm 11 01076 g001 550
Figure 1. Percentage of clinical response, clinical remission, endoscopic response, endoscopic remission, and adverse events for each combination therapy.
Ustekinumab plus vedolizumab
Yang et al. [9] reported the results of eight patients who received treatment with the combination of ustekinumab and vedolizumab. During follow-up at week 40, five of seven (71%) patients achieved clinical response, four of seven (57%) achieved clinical remission, five of eight (63%) achieved endoscopic improvement, and two of eight (25%) achieved endoscopic remission. The adverse event rate was low—one of eight (13%) patients.
Anti-TNF plus vedolizumab
Privitera et al. [10] reported results in six patients. Three of six (50%) patients had a clinical response and three of six had clinical remission (50%) at 6 month follow-up. Only one adverse event was reported in one patient (16.6%), who presented a cutaneous rash.
Other combinations
Privitera et al. [10] reported results in four patients on anti-TNF plus ustekinumab; one patient had a clinical response and three had clinical remission at 6 month follow-up.
Glassner et al. [11] reported eight patients on vedolizumab plus tofacitinib, nine patients on anti-TNF plus tofacitinib, and three patients on tofacitinib plus ustekinumab. However, individual results were not available.
Safety

Table 1 shows the rates of clinical response, clinical remission, endoscopic response, endoscopic remission, and adverse event rates for each CoT.

Table 1. Results for clinical response, clinical remission, endoscopic response, endoscopic remission, and adverse events for each combination.
    Clinical Response Clinical Remission Endoscopic Response Endoscopic Remission Adverse Events
Ustekinumab + Vedolizumab Yang et al. 5 of 7 4 of 7 5 of 8 2 of 8 1 of 8
Kwapisz et al. 4 of 5       0 of 5
Privitera et al. 3 of 3       1 of 3
Glassner et al.     11 of 13    
TOTAL 12 of 15 (80%) 4 of 7 (57%) 16 of 21 (76%) 2 of 8 (25%) 2 of 11 (18%)
Anti-TNF + Vedolizumab Yang et al. 5 of 12 4 of 12 4 of 12 3 of 12 2 of 12
Kwapisz et al. 5 of 8       3 of 8
Privitera et al. 3 of 6 3 of 6     1 of 6
Glassner et al.     24 of 36    
TOTAL 13 of 26 (50%) 7 of 18 (29%) 28 of 48 (58%) 3 of 12 (25%) 5 of 26 (19%)
Anti-TNF + Ustekinumab Yang et al. 1 of 3 1 of 3 1 of 3 1 of 3  
Kwapisz et al. 2 of 2        
Privitera et al. 1 of 4 3 of 4      
TOTAL 4 of 9 (44%) 4 of 7 (57%) 1 of 3 (33%) 1 of 3 (33%)  
Secukinumab + Vedolizumab Privitera et al. 2 of 2        
TOTAL 2 of 2 (100%)        
Vedolizumab + Apremilast Privitera et al. 1 of 1       1 of 1
TOTAL 1 of 1 (100%)       1 of 1 (100%)
Vedolizumab + Tofacitinib Glassner et al.     8 of 12    
TOTAL     8 of 12 (67%)  

4. Summary

The most-used CoTs are shown in Table 2. Of them, vedolizumab plus ustekinumab and vedolizumab plus anti-TNF were the most effective CoTs for CD. Furthermore, vedolizumab plus anti-TNF and vedolizumab plus tofacitinib were the most effective CoTs for UC. The combination of ustekinumab and vedolizumab seems especially attractive because it might combine efficacy, safety, and persistence over time. Very recently, Stone et al. reported similarly good results in a retrospective series of 10 patients [12]. Data are preliminary and, in patients with UC and uncontrolled extraintestinal manifestations, CoT including anti-TNF or tofacitinib might be more effective.

Table 2. Most used combinations.
Study VEDO+
USTE		 AntiTNF+
VEDO		 AntiTNF+
USTE		 TOFA+
VEDO		 TOFA+
USTE		 TOFA+
TNF		 Other **
Goessens et al. * [13] 16 36 8 12 - 1 8
Glassner et al. [11] 25 7   8 3 9 1
Kwapisz et al. [14] 5 8 2        
Privitera et al. ** [10] 3 6 4       3
Yang et al. [9] 8 13 3        
TOTAL 62 75 20 21 3 10 19
VEDO (vedolizumab), USTE (ustekinumab), TOFA (tofacitinib). * CoTs used for extraintestinal manifestations were excluded. ** Other molecules used: apremilast, cyclosporine, rituximab, secukinumab, leflunomide, and tacrolimus.
CoT has also been explored in other clinical settings, such as the treatment of psoriasis with associated joint manifestations. In these patients, treatment was effective and there was no increase in adverse events [15][16][17]. Otherwise, the combinations used for the treatment of rheumatoid arthritis demonstrated good efficacy but an increase in the rate of adverse events [18][19][20][21]. In IBD, CoT has even been used in pediatric patients with good results and safety [22][23].
In conclusion, IBD treatment is still rapidly evolving. Along with the new therapies that are rapidly becoming available, CoT has demonstrated promising results and may represent a new opportunity to improve both patients’ quality of life and long-term prognosis. However, current data are very limited, and larger studies with longer follow-up are desirable to confirm the safety and efficacy of CoT. In the meantime, CoT seems a real alternative for refractory and severely ill patients who cannot wait for new developments to come.

References

  1. Raine, T.; Bonovas, S.; Burisch, J.; Kucharzik, T.; Adamina, M.; Annese, V.; Bachmann, O.; Bettenworth, D.; Chaparro, M.; Czuber-Dochan, W.; et al. ECCO Guidelines on Therapeutics in Ulcerative Colitis: Medical Treatment. J. Crohn’s Colitis 2021, 16, 2–17.
  2. Torres, J.; Bonovas, S.; Doherty, G.; Kucharzik, T.; Gisbert, J.P.; Raine, T.; Adamina, M.; Armuzzi, A.; Bachmann, O.; Bager, P.; et al. ECCO Guidelines on Therapeutics in Crohn’s Disease: Medical Treatment. J. Crohn’s Colitis 2020, 14, 4–22.
  3. Colombel, J.F.; Reinisch, W.; Mantzaris, G.J.; Kornbluth, A.; Rutgeerts, P.; Tang, K.L.; Oortwijn, A.; Bevelander, G.S.; Cornillie, F.J.; Sandborn, W.J. Randomised clinical trial: Deep remission in biologic and immunomodulator naïve patients with Crohn’s disease—A SONIC post hoc analysis. Aliment. Pharmacol. Ther. 2015, 41, 734–746.
  4. Hirten, R.P.; Iacucci, M.; Shah, S.; Ghosh, S.; Colombel, J.F. Combining Biologics in Inflammatory Bowel Disease and Other Immune Mediated Inflammatory Disorders. Clin. Gastroenterol. Hepatol. 2018, 16, 1374–1384.
  5. Grieco, M.J.; Remzi, F.H. Surgical Management of Ulcerative Colitis. Gastroenterol. Clin. N. Am. 2020, 49, 753–768.
  6. Ricart, E. Current status of mesenchymal stem cell therapy and bone marrow transplantation in IBD. Dig. Dis. 2012, 30, 387–391.
  7. Gold, S.L.; Steinlauf, A.F. Therapy in Patients With Inflammatory Bowel Disease: A Review of the Literature. Gastroenterol. Hepatol. 2021, 17, 406–414.
  8. Ribaldone, D.G.; Pellicano, R.; Vernero, M.; Caviglia, G.P.; Saracco, G.M.; Morino, M.; Astegiano, M. Dual biological therapy with anti-TNF, vedolizumab or ustekinumab in inflammatory bowel disease: A systematic review with pool analysis. Scand. J. Gastroenterol. 2019, 54, 407–413.
  9. Yang, E.; Panaccione, N.; Whitmire, N.; Dulai, P.S.; Casteele, N.V.; Singh, S.; Boland, B.S.; Collins, A.; Sandborn, W.J.; Panaccione, R.; et al. Efficacy and Safety of Simultaneous Treatment with Two Biologic Medications in Refractory Crohn’s Disease. Aliment. Pharmacol. Ther. 2020, 51, 1031–1038.
  10. Privitera, G.; Onali, S.; Pugliese, D.; Renna, S.; Savarino, E.; Viola, A.; Ribaldone, D.G.; Buda, A.; Bezzio, C.; Fiorino, G.; et al. Dual Targeted Therapy: A Possible Option for the Management of Refractory Inflammatory Bowel Disease. J. Crohn’s Colitis 2021, 15, 335–339.
  11. Glassner, K.; Oglat, A.; Duran, A.; Koduru, P.; Perry, C.; Wilhite, A.; Abraham, B.P. The use of combination biological or small molecule therapy in inflammatory bowel disease: A retrospective cohort study. J. Dig. Dis. 2020, 21, 264–271.
  12. Stone, M.; Morrison, M.; Forster, E. P076 The Role of Dual Biologic Therapy in Inflammatory Bowel Disease. Am. J. Gastroenterol. 2021, 116, S20.
  13. Goessens, L.; Colombel, J.F.; Outtier, A.; Ferrante, M.; Sabino, J.; Judge, C.; Saeidi, R.; Rabbitt, L.; Armuzzi, A.; Domenech, E.; et al. Safety and efficacy of combining biologics or small molecules for inflammatory bowel disease or immune-mediated inflammatory diseases: A European retrospective observational study. United Eur. Gastroenterol. J. 2021, 9, 1136–1147.
  14. Kwapisz, L.; Raffals, L.E.; Bruining, D.H.; Pardi, D.S.; Tremaine, W.J.; Kane, S.V.; Papadakis, K.A.; Coelho-Prabhu, N.; Kisiel, J.B.; Heron, V.; et al. Combination Biologic Therapy in Inflammatory Bowel Disease: Experience From a Tertiary Care Center. Clin. Gastroenterol. Hepatol. 2021, 19, 616–617.
  15. Gniadecki, R.; Bang, B.; Sand, C. Combination of antitumour necrosis factor-α and anti-interleukin-12/23 antibodies in refractory psoriasis and psoriatic arthritis: A long-term case-series observational study. Br. J. Dermatol. 2016, 174, 1145–1146.
  16. Hamilton, T. Treatment of psoriatic arthritis and recalcitrant skin disease with combination therapy. J. Drugs Dermatol. 2008, 7, 1089–1093.
  17. Krell, J.M. Use of alefacept and etanercept in 3 patients whose psoriasis failed to respond to etanercept. J. Am. Acad. Dermatol. 2006, 54, 1099–1101.
  18. Weinblatt, M.; Combe, B.; Covucci, A.; Aranda, R.; Becker, J.C.; Keystone, E. Safety of the selective costimulation modulator abatacept in rheumatoid arthritis patients receiving background biologic and nonbiologic disease-modifying antirheumatic drugs: A one-year randomized, placebo-controlled study. Arthritis Rheum. 2006, 54, 2807–2816.
  19. Weinblatt, M.; Schiff, M.; Goldman, A.; Kremer, J.; Luggen, M.; Li, T.; Chen, D.; Becker, J.C. Selective costimulation modulation using abatacept in patients with active rheumatoid arthritis while receiving etanercept: A randomised clinical trial. Ann. Rheum. Dis. 2007, 66, 228–234.
  20. Greenwald, M.W.; Shergy, W.J.; Kaine, J.L.; Sweetser, M.T.; Gilder, K.; Linnik, M.D. Evaluation of the safety of rituximab in combination with a tumor necrosis factor inhibitor and methotrexate in patients with active rheumatoid arthritis: Results from a randomized controlled trial. Arthritis Rheum. 2011, 63, 622–632.
  21. Van Vollenhoven, R.F.; Wax, S.; Li, Y.; Tak, P.P. Safety and efficacy of atacicept in combination with rituximab for reducing the signs and symptoms of rheumatoid arthritis: A phase II, randomized, double-blind, placebo-controlled pilot trial. Arthritis Rheumatol. 2015, 67, 2828–2836.
  22. Olbjørn, C.; Rove, J.B.; Jahnsen, J. Combination of Biological Agents in Moderate to Severe Pediatric Inflammatory Bowel Disease: A Case Series and Review of the Literature. Pediatr. Drugs 2020, 22, 409–416.
  23. Dolinger, M.; Spencer, E.; Lai, J.; Dunkin, D.; Dubinsky, M. Dual biologic and small molecule therapy for the treatment of refractory pediatric inflammatory bowel disease. Inflamm. Bowel Dis. 2021, 27, 1210–1214.
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Eduard Brunet
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