Efficacy and Safety of Long-Term Thiopurine Maintenance Treatment in Japanese Patients With Ulcerative Colitis

Satoshi Yamada; Takuya Yoshino; Minoru Matsuura; Masamichi Kimura; Yorimitsu Koshikawa; Naoki Minami; Takahiko Toyonaga; Yusuke Honzawa; Hiroshi Nakase

doi:10.5217/ir.2015.13.3.250

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Original Article Efficacy and Safety of Long-Term Thiopurine Maintenance Treatment in Japanese Patients With Ulcerative Colitis: Satoshi Yamada¹, Takuya Yoshino¹, Minoru Matsuura¹, Masamichi Kimura¹, Yorimitsu Koshikawa¹, Naoki Minami¹, Takahiko Toyonaga², Yusuke Honzawa¹, Hiroshi Nakase¹; Intestinal Research 2015;13(3):250-258.
DOI: https://doi.org/10.5217/ir.2015.13.3.250
Published online: June 9, 2015

¹Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

²The Third Department of Internal Medicine, Kansai Medical University, Osaka, Japan.

Correspondence to Hiroshi Nakase, Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan. Tel: +81-75-751-4319, Fax: +81-75-751-4303, hiropy_n@kuhp.kyoto-u.ac.jp

• Received: December 19, 2014 • Revised: February 19, 2015 • Accepted: February 24, 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Abstract
INTRODUCTION
METHODS
RESULTS
DISCUSSION
NOTES
Supplementary Material
REFERENCES

Abstract

Background/Aims
The long-term clinical outcomes of patients with bio-naive ulcerative colitis (UC) who maintain remission with thiopurine are unclear. The aim of this study was to assess the long-term efficacy and safety of maintenance treatment with thiopurine in UC patients.
Methods
This was a retrospective observational cohort analysis conducted at a single center. Between December 1998 and August 2013, 59 of 87 patients with bio-naive UC who achieved remission after induction with treatments other than biologics were enrolled. Remission maintenance with thiopurine was defined as no concomitant treatment needed other than 5-aminosalicylate without relapse. We assessed the remission-maintenance rate, mucosal healing rate, colectomy-free rate, and treatment safety in UC patients who received thiopurine as maintenance treatment.
Results
The 84-month cumulative remission-maintenance and colectomy-free survival rates in the UC patients who were receiving maintenance treatment with thiopurine and 5-aminosalicylate were 43.9% and 88.0%, respectively. Of the 38 patients who underwent colonoscopy during thiopurine maintenance treatment, 23 (60.5%) achieved mucosal healing. Of the 59 patients who achieved clinical remission with thiopurine, 6 patients (10.2%) discontinued the thiopurine therapy because of adverse events.
Conclusions
Our study demonstrates the long-term efficacy and safety of thiopurine treatment in patients with bio-naive UC.
Keywords: Thiopurine; Colitis, ulcerative; Maintenance treatment

INTRODUCTION

Ulcerative colitis (UC) is a lifelong immune-mediated inflammatory condition of the colonic mucosa that is characterized by a relapsing and remitting course.1 2 Sustained inflammation in patients with UC results in a progressive worsening of their quality of life.3 Most UC patients are successfully managed with mesalamine formulations, but in approximately 25% of UC patients, mesalamine treatment or other therapies fail, thus requiring intensified treatment or colectomy.4 Corticosteroids remain a mainstay for inducing remission in patients with moderate to severe UC, but their long-term use is not recommended because of adverse side effects.5 6 7 The investigators of one European cohort study that included a large number of UC patients reported that at 1 year after withdrawal of corticosteroid treatment, fewer than half of the patients had a sustained response, one-third required colectomy, and approximately one-fourth required reinduction of corticosteroid treatment due to a UC relapse.8 Thus, the maintenance of steroid-free remission in UC patients is a clinically important issue.

Thiopurines, azathioprine (AZA) and its metabolite 6-mercaptopurine (6-MP) are purine analogs that effectively induce and maintain remission in patients with IBD, particularly in steroid-refractory or steroid-dependent disease.9 10 Although the effects of thiopurine on refractory IBD are apparent in clinical practice, only a few prospective studies and one meta-analysis have been reported.10 11 12 Moreover, little is known about the long-term clinical outcome of UC patients who initially responded to thiopurine treatment.

The efficacy of biologics such as infliximab and adalimumab for induction of remission and maintenance in UC patients has been reported.13 14 15 16 Clinical trials, case series, and a meta-analysis have demonstrated the benefits of these biologic therapies for UC patients.13 14 15 16 17 18 19 The costliness of the long-term use of biologics, however, is problematic.20 In addition, observational data suggest that patients taking biologics are at increased risk of opportunistic infection.21 Therefore, the usefulness of thiopurine for maintaining remission in UC patients must be reconsidered. The aim of this study was to assess the long-term efficacy and safety of maintenance treatment with thiopurine in Japanese patients with UC.

METHODS

1. Study Design

This was a single-center retrospective cohort study. All patients with UC at Kyoto University Hospital who were treated with a thiopurine and 5-aminosalicylate (5-ASA) formulation as maintenance treatment after induction treatments such as 5-ASA, corticosteroids, granulocyte-monocyte adsorption apheresis (GMAA), and calcineurin inhibitors between December 1998 and August 2013 were enrolled in the study. All of the subjects provided informed consent. The study protocol conformed to the Declaration of Helsinki and was approved by the Institutional Review Board at Kyoto University Hospital.

2. Definition of UC

The diagnosis of UC was confirmed by reviewing endoscopic and pathological reports. Disease activity was evaluated based on a modified Truelove and Witts Severity Index (MTWSI) score (Supplemental Table 1).22 23 24 Clinical remission was defined as an MTWSI score lower than 4. UC relapse was defined as an MTWSI score increase of at least 3 points from baseline leading to treatment modification. UC flare-up was defined as an increase in MTWSI score of at least 3 points from the baseline and leading to treatment modification.24 Refractory UC was defined as (1) steroid refractory, or the lack of a clinical response to a systemic daily dose of 30 mg or more of prednisolone over at least 2 weeks; and (2) steroid dependency, or failing to taper the prednisolone dose to less than 10 mg/day within 12 weeks or relapse within 12 weeks after prednisolone discontinuation. Mucosal healing was defined as endoscopic findings with a Mayo score of 0 or 1.13 The time to colonoscopy was different for each patient because this study was retrospective.

To assess mucosal healing, follow-up colonoscopy was routinely performed after clinical remission in UC patients whose corticosteroid dose were completely tapered off.

AZA and 6-MP were administered as thiopurines. We generally administered AZA, and we used 6-MP in patients intolerant to AZA. The thiopurine dose was optimized to achieve a white blood cell count between 3,000 and 5,000/µL or a 6-thioguanine nucleotide concentration between 235 and 450 pmol/8×10⁸ erythrocytes. For UC patients enrolled in this study, induction treatments included 5-ASA, corticosteroids, GMAA, and calcineurin inhibitors such as tacrolimus and cyclosporine. The tacrolimus dose was adjusted to produce consistent trough levels of 10 to 15 ng/mL, and the dose of cyclosporine was adjusted to produce consistent trough levels of 150 to 250 ng/mL.

3. Assessment

The primary endpoint of this study was the remission-maintenance rate with thiopurine and 5-ASA in the UC patients. Secondary endpoints were the predictive factors, namely flare-up, mucosal healing rate, and colectomy-free survival in UC patients treated with thiopurine and 5-ASA.

4. Statistical Analysis

Normally distributed continuous variables were analyzed by using Student's t-test, and nonparametric data were analyzed with Wilcoxon's rank sum test. Categorical variables were analyzed by using Pearson's chi-square test or Fisher's exact test if any cell number was less than 5. A P<0.05 was considered as statistically significant. Cumulative colectomy-free and remission-maintenance rates were assessed by using the Kaplan-Meier method, and groups were compared by using the log-rank test stratified by study. Predictive factors were analyzed with multivariate statistics by using Cox regression. All analyses were performed by using the Statview software (SAS Institute, Cary, NC, USA).

RESULTS

1. Patient Characteristics

Of the 87 UC patients who received various induction therapies, including 5-ASA, GMAA, corticosteroids, or calcineurin inhibitors, 68 (78.2%) achieved a clinical response with induction treatment and thiopurine. Of the 68 patients, 59 (67.8%) maintained clinical remission with thiopurine and 5-ASA after tapering the dose in the induction treatment (Fig. 1A). Of these 59 patients, 3 (5.1%) discontinued thiopurine treatment because of adverse events, and the remaining 56 patients (94.9%) were evaluated in the present study.

The characteristics of the 56 patients who were undergoing maintenance therapy with thiopurine and 5-ASA are shown in Table 1. Of the 56 patients, 38 (67.9%) were men and 18 (32.2%) were women, with a median age of 31.5 years (range, 13-83 years). The median disease duration from diagnosis of UC to initiation of thiopurine treatment was 33.5 months (range, 1-292 months). Three of the 56 patients (5.4%) had proctitis, 16 (28.6%) had left-sided colitis, and the remaining 37 (66.0%) had extensive colitis. Of the 56 patients, 39 (69.6%) had refractory UC (steroid dependent in 30 patients [76.9%] and steroid refractory in 9 patients [23.1%]). The median MTWSI score at the initiation of the thiopurine treatment was 5.0 points (range, 0-13 points). The median Mayo endoscopic score at the time of thiopurine initiation was 2.0 points (range, 1-3 points). In 52 (94.5%) of the 56 patients, 5-ASA was used for induction treatment. GMAA was used in 4 (7.1%), corticosteroids in 26 (46.4%), and a calcineurin inhibitor (tacrolimus/cyclosporine) in 14 (25.0%).

2. Clinical Remission Maintenance in UC Patients Who Were Receiving Thiopurine and 5-ASA as Maintenance Treatment

Of the 56 patients, 47 (83.9%) were treated with AZA and 9 (16.1%) were treated with 6-MP. The median dose of thiopurine during the maintenance treatment was 50 mg (range, 10-135 mg), although 4 patients (7.1%) received concomitant allopurinol to increase the 6-thioguanine nucleotide concentration. 6-Thioguanine nucleotide concentration was evaluated in 37 (66.1%) of the 56 patients, and the median 6-thioguanine nucleotide concentration was 358.8 pmol/8×10⁸ erythrocytes (range, 50-1,670 pmol/8×10⁸ erythrocytes). In addition, 52 (94.5%) of the 56 patients received concomitant 5-ASA, and the median 5-ASA dose was 3,000 mg (range, 250-4,000 mg) during thiopurine maintenance treatment.

Of the 56 patients, 37 (66.1%) were maintained in clinical remission with thiopurine and 5-ASA (remission group), while 19 (33.9%) had a UC relapse during the study period (relapse group). Six UC patients discontinued thiopurine due to adverse events. However, 3 of them experienced a UC relapse at the onset of adverse events and were included in the relapse group (Fig. 1A). The median follow-up duration after initiating thiopurine in the 56 patients who achieved clinical remission was 33.0 months (range, 4-143 months). Based on the Kaplan-Meier analysis, the cumulative remission-maintenance rates in the 56 patients treated with thiopurine and 5-ASA after the dose in the induction treatment was tapered were estimated to be 43.9% at 84 months, 94.3% at 6 months, 84.6% at 12 months, 69.0% at 24 months, 54.9% at 48 months, 54.9% at 72 months, and 43.9% at 84 months, respectively (Fig. 1B).

3. Predictive Factors of Maintaining Remission With Thiopurine

To evaluate the predictive factors of maintaining remission with thiopurine, we evaluated the differences in the patient characteristics between the remission and relapse groups. The number of UC patients with a history of corticosteroid use (≥40 mg/day) differed significantly between the remission and relapse groups (Table 1). According to the Kaplan-Meier analysis, the cumulative remission-maintenance rate was significantly lower in the UC patients with than in those without a history of treatment with a corticosteroid dosage ≥40 mg/day (12.1% at 83 months vs. 51.5% at 84 months, P=0.032). Moreover, the multivariate analysis using Cox regression suggested that history of treatment with a corticosteroid dosage ≥40 mg/day was indicated as a negative predictive factor of clinical remission maintenance in UC patients (hazard ratio, 3.76; P=0.01) (Table 2).

4. Mucosal Healing for UC Patients Receiving Maintenance Treatment With Thiopurine and 5-ASA

Of the 56 UC patients, 38 (67.9%) underwent colonoscopy to evaluate mucosal healing, and the median time to assessing mucosal healing after initiating thiopurine agents was 26.8 months (range, 1-84 months). Among the 38 patients, 23 (60.5%) achieved mucosal healing (mucosal healing group) and 15 (39.5%) did not achieve mucosal healing (non-mucosal healing group). To evaluate the predictive factors of mucosal healing in the UC patients who maintained clinical remission with thiopurine, we analyzed the differences in patient characteristics between the mucosal and non-mucosal healing groups. The serum CRP concentration and number of UC patients with a history of corticosteroid treatment ≥40 mg/day tended to be greater in the non-mucosal healing group than in the mucosal healing group, although no significant differences in patient characteristics were observed between the mucosal and non-mucosal healing groups (Table 3). Based on the multivariate analysis (Table 4), CRP elevation was a negative factor of mucosal healing (hazard ratio, 1.46; P=0.03).

5. Colectomy-Free Rate Among UC Patients Who Achieved Steroid-Free Remission With Thiopurine and 5-ASA

Of the 56 patients, 2 (3.6%) underwent colectomy due to a UC relapse under steroid-free remission. Based on the Kaplan-Meier analysis, the estimated cumulative colectomy-free rate of the UC patients whose remission was maintained with thiopurine was 88.0% at 84 months (Fig. 1C).

6. Adverse Events

Adverse events occurred in 17 (28.8%) of the 59 patients who achieved clinical remission with thiopurine and 5-ASA (Table 5). Moreover, 6 (10.2%) of the 59 patients discontinued thiopurine treatment because of adverse events. Adverse events requiring withdrawal of thiopurine treatment included infectious mononucleosis (1 patient, 1.7%), nausea (1 patients, 1.7%), liver dysfunction (2 patients, 3.4%), pancreatitis (1 patient, 1.7%), and leukopenia (1 patients, 1.7%). All of the patients recovered from adverse events upon discontinuation of thiopurine, and no mortality due to adverse events occurred during the follow-up.

DISCUSSION

The findings of the present study demonstrate the long-term efficacy and safety of thiopurine for maintaining remission in bio-naive UC patients. A history of treatment with high-dose corticosteroids affects both the maintenance of remission and mucosal healing in bio-naive UC patients treated with thiopurine.

Recently, many papers reported the efficacy of biologics for the induction and maintenance of remission in refractory UC patients.13 14 15 16 17 18 19 Induction and maintenance of long-term remission in patients with mild to moderate bio-naive UC, however, should also be considered. Controlled studies have demonstrated that thiopurines are effective for steroid tapering and maintenance of remission in UC patients.11 Several meta-analyses also demonstrated the efficacy of thiopurine for the induction and maintenance of remission in UC.9 10 11 12 25 26 In the present study, clinical remission was maintained with thiopurine in 66.1% of the bio-naive UC patients, suggesting the high efficacy of thiopurine for maintenance of remission in UC patients.

The identification of UC patients in whom clinical remission can be maintained with thiopurine is highly important for long-term treatment of UC. Nquyen et al. reported that factors such as age, sex, patient adherence, duration of treatment with thiopurine, erythrocyte count, and erythrocyte sedimentation rate could not predict the efficacy of thiopurine.27 Interestingly, our data revealed that corticosteroid treatment, particularly in those with a history of high-dose corticosteroid use, might be a negative predictive factor of maintaining remission with thiopurine in UC patients. Thus, high-dose corticosteroids should be avoided for successful management of UC patients.

The aims of UC treatment should include the promotion of mucosal healing and the induction and maintenance of clinical remission, because several reports indicate that mucosal healing reduces the rate of hospitalization and colectomy, improving patient quality of life.13 28 29 Data regarding the usefulness of thiopurine for achieving and maintaining mucosal healing in UC patients, however, are limited. In a cohort study with a small number of UC patients reported by Lopez et al., 60% of UC patients who maintained remission with thiopurine also achieved and maintained mucosal healing.28 Endoscopic activity might be predictive of flare-up in UC patients, even if clinical remission is maintained. The present study revealed that the mucosal healing rate in UC patients who maintained remission with thiopurine treatment (60.5%) was similar to that in the study of Lopez et al.28 and suggests that a high CRP concentration is a negative predictor of mucosal healing. Previous studies demonstrated the positive correlation between CRP level and the drgree of mucosal inflammation evaluated by using endoscopy, especially in severe UC.30 31 32 High doses and long-term use of corticosteroids could affect epithelial regeneration by inhibiting nuclear factor kappa B activation in epithelial cells,33 even if thiopurines are selected for maintenance treatment. In this regard, the use of high-dose corticosteroids for the treatment of UC should be avoided as much as possible.

Previous reports indicated that treatment with thiopurine may increase the risk of life-threatening adverse events, particularly malignancies.34 35 36 37 The guidelines of the European Crohn's and Colitis Organization, however, recommend thiopurine as a first-line treatment for refractory UC patients who experience a UC flare-up during corticosteroid withdrawal.38 In the present study, adverse events occurred in 27.1% of the UC patients treated with thiopurine. The frequency of adverse events in our study was similar to that in previous reports26 34 35 Moreover, no life-threatening infections or malignancies occurred in the observational period (7 years). Roblin et al.39 reported that an optimal dose of thiopurine might help to prevent severe adverse events. Therefore, monitoring 6-thioguanine nucleotide levels is required for maintenance of long-term remission and the prevention of adverse events in UC patients treated with thiopurine.

The present study has several limitations, including the small number of patients and the single-center, retrospective design. In addition, the time to assess endoscopic activity after achieving clinical remission varied. Therefore, our data should be interpreted with caution, and further studies with a larger number of enrolled patients are required.

In conclusion, our long-term observational data indicate that thiopurine is useful for maintaining remission and promoting mucosal healing in bio-naive UC patients. Optimal use of thiopurine will contribute to long-term remission in bio-naive UC patients.

NOTES

Financial support: This work was supported by the Japanese Society for the Promotion of Science "KAKENHI" Grants-in-Aid for Scientific Research (Nos. 24590941, 25860532, 26460967, and 26893122) and Health and Labour Sciences Research Grants for Research on Rare and Intractable Disease from the Ministry of Health, Labour and Welfare, Japan.

Conflict of interest: None.

Supplementary Material

ir-13-250-s001.pdf

Supplemental Table 1

Modified Truelove and Witts Severity Index Score

Score	0	1	2	3	4	5
Bowel movement	0-2	3-4	5-6	7-9	≤10
Nocturnal diarrhea	No	Yes
Visible blood in stool (%)	0	<50	≤50	100
Abdominal tenderness	None	Mild	Moderate	Severe
Abdominal pain/cramping	None	Mild	Moderate	Severe
Need for antidiarrheals	No	Yes
General status	Perfect	Very good	Good	Average	Poor	Terrible
Fecal incontinence	No	Yes

Severe disease, ≤12; mild to moderate, 5-11; remission category, ≤4

REFERENCES

1. MacDermott RP, Stenson WF. Alterations of the immune system in ulcerative colitis and Crohn's disease. Adv Immunol 1988;42:285–328.PMID: 3284291.Article PubMed
2. Monteleone I, Vavassori P, Biancone L, Monteleone G, Pallone F. Immunoregulation in the gut: success and failures in human disease. Gut 2002;50(Suppl 3): III60–III64.PMID: 11953335.Article PubMed PMC
3. Hanauer SB. Review article: evolving concepts in treatment and disease modification in ulcerative colitis. Aliment Pharmacol Ther 2008;27(Suppl 1): 15–21.PMID: 18307645.Article PubMed
4. Sutherland LR, Martin F, Bailey RJ, et al. The Canadian Mesalamine for Remission of Crohn's Disease Study Group. A randomized, placebo-controlled, double-blind trial of mesalamine in the maintenance of remission of Crohn's disease. Gastroenterology 1997;112:1069–1077.PMID: 9097988.Article PubMed
5. Kozuch PL, Hanauer SB. Treatment of inflammatory bowel disease: a review of medical therapy. World J Gastroenterol 2008;14:354–377.PMID: 18200659.Article PubMed PMC
6. Carter MJ, Lobo AJ, Travis SP. IBD Section, British Society of Gastroenterology. Guidelines for the management of inflammatory bowel disease in adults. Gut 2004;53(Suppl 5): V1–V16.PMID: 15306569.Article PubMed PMC
7. Irving PM, Gearry RB, Sparrow MP, Gibson PR. Review article: appropriate use of corticosteroids in Crohn's disease. Aliment Pharmacol Ther 2007;26:313–329.PMID: 17635367.Article PubMed
8. Faubion WA Jr, Loftus EV Jr, Harmsen WS, Zinsmeister AR, Sandborn WJ. The natural history of corticosteroid therapy for inflammatory bowel disease: a population-based study. Gastroenterology 2001;121:255–260.PMID: 11487534.Article PubMed
9. Costantino G, Furfaro F, Belvedere A, Alibrandi A, Fries W. Thiopurine treatment in inflammatory bowel disease: response predictors, safety, and withdrawal in follow-up. J Crohns Colitis 2012;6:588–596.PMID: 22398045.Article PubMed PDF
10. Chebli LA, Chaves LD, Pimentel FF, et al. Azathioprine maintains long-term steroid-free remission through 3 years in patients with steroid-dependent ulcerative colitis. Inflamm Bowel Dis 2010;16:613–619.PMID: 19705415.Article PubMed
11. Ardizzone S, Maconi G, Russo A, Imbesi V, Colombo E, Bianchi Porro G. Randomised controlled trial of azathioprine and 5-aminosalicylic acid for treatment of steroid dependent ulcerative colitis. Gut 2006;55:47–53.PMID: 15972298.Article PubMed PMC
12. Timmer A, McDonald JW, Macdonald JK. Azathioprine and 6-mercaptopurine for maintenance of remission in ulcerative colitis. Cochrane Database Syst Rev 2007;CD000478PMID: 10.1002/14651858.CD000478.pub2. Published online 24 January 2007. PMID: 17253451.Article PubMed
13. Rutgeerts P, Sandborn WJ, Feagan BG, et al. Infliximab for induction and maintenance therapy for ulcerative colitis. N Engl J Med 2005;353:2462–2476.PMID: 16339095.Article PubMed
14. Probert CS, Hearing SD, Schreiber S, et al. Infliximab in moderately severe glucocorticoid resistant ulcerative colitis: a randomised controlled trial. Gut 2003;52:998–1002.PMID: 12801957.Article PubMed PMC
15. Reinisch W, Sandborn WJ, Hommes DW, et al. Adalimumab for induction of clinical remission in moderately to severely active ulcerative colitis: results of a randomised controlled trial. Gut 2011;60:780–787.PMID: 21209123.Article PubMed
16. Sandborn WJ, van Assche G, Reinisch W, et al. Adalimumab induces and maintains clinical remission in patients with moderate-to-severe ulcerative colitis. Gastroenterology 2012;142:257–265.PMID: 22062358.Article PubMed
17. Stidham RW, Lee TC, Higgins PD, et al. Systematic review with network meta-analysis: the efficacy of anti-tumour necrosis factor-alpha agents for the treatment of ulcerative colitis. Aliment Pharmacol Ther 2014;39:660–671.PMID: 24506179.Article PubMed PMC
18. Sandborn WJ, Feagan BG, Marano C, et al. Subcutaneous golimumab induces clinical response and remission in patients with moderate-to-severe ulcerative colitis. Gastroenterology 2014;146:85–95.PMID: 23735746.Article PubMed
19. Sandborn WJ, Feagan BG, Marano C, et al. Subcutaneous golimumab maintains clinical response in patients with moderate-to-severe ulcerative colitis. Gastroenterology 2014;146:96–109.PMID: 23770005.Article PubMed
20. Dretzke J, Edlin R, Round J, et al. A systematic review and economic evaluation of the use of tumour necrosis factor-alpha (TNF-alpha) inhibitors, adalimumab and infliximab, for Crohn's disease. Health Technol Assess 2011;15:1–244.PMID: 21291629.Article PDF
21. Ford AC, Peyrin-Biroulet L. Opportunistic infections with anti-tumor necrosis factor-alpha therapy in inflammatory bowel disease: meta-analysis of randomized controlled trials. Am J Gastroenterol 2013;108:1268–1276.PMID: 23649185.Article PubMed PDF
22. Lichtiger S, Present DH, Kornbluth A, et al. Cyclosporine in severe ulcerative colitis refractory to steroid therapy. N Engl J Med 1994;330:1841–1845.PMID: 8196726.Article PubMed
23. Yamamoto S, Nakase H, Mikami S, et al. Long-term effect of tacrolimus therapy in patients with refractory ulcerative colitis. Aliment Pharmacol Ther 2008;28:589–597.PMID: 18549460.Article PubMed
24. Laharie D, Bourreille A, Branche J, et al. Ciclosporin versus infliximab in patients with severe ulcerative colitis refractory to intravenous steroids: a parallel, open-label randomised controlled trial. Lancet 2012;380:1909–1915.PMID: 23063316.Article PubMed
25. Gisbert JP, Linares PM, McNicholl AG, Maté J, GomollÓn F. Meta-analysis: the efficacy of azathioprine and mercaptopurine in ulcerative colitis. Aliment Pharmacol Ther 2009;30:126–137.PMID: 19392869.Article PubMed
26. Khan KJ, Dubinsky MC, Ford AC, Ullman TA, Talley NJ, Moayyedi P. Efficacy of immunosuppressive therapy for inflammatory bowel disease: a systematic review and meta-analysis. Am J Gastroenterol 2011;106:630–642.PMID: 21407186.Article PubMed PDF
27. Nguyen TV, Vu DH, Nguyen TM, Lachaux A, Boulieu R. Exploring associations of 6-thioguanine nucleotide levels and other predictive factors with therapeutic response to azathioprine in pediatric patients with IBD using multilevel analysis. Inflamm Bowel Dis 2013;19:2404–2410.PMID: 24013359.Article PubMed
28. LÓpez-Palacios N, Mendoza JL, Taxonera C, Lana R, LÓpez-Jamar JM, Díaz-Rubio M. Mucosal healing for predicting clinical outcome in patients with ulcerative colitis using thiopurines in monotherapy. Eur J Intern Med 2011;22:621–625.PMID: 22075292.Article PubMed
29. Dave M, Loftus EV Jr. Mucosal healing in inflammatory bowel disease-a true paradigm of success? Gastroenterol Hepatol (N Y) 2012;8:29–38.PMID: 22347830.PubMed PMC
30. Rosenberg L, Nanda KS, Zenlea T, et al. Histologic markers of inflammation in patients with ulcerative colitis in clinical remission. Clin Gastroenterol Hepatol 2013;11:991–996.PMID: 23591275.Article PubMed PMC
31. Solem CA, Loftus EV Jr, Tremaine WJ, Harmsen WS, Zinsmeister AR, Sandborn WJ. Correlation of C-reactive protein with clinical, endoscopic, histologic, and radiographic activity in inflammatory bowel disease. Inflamm Bowel Dis 2005;11:707–712.PMID: 16043984.Article PubMed
32. Schoepfer AM, Beglinger C, Straumann A, Trummler M, Renzulli P, Seibold F. Ulcerative colitis: correlation of the Rachmilewitz endoscopic activity index with fecal calprotectin, clinical activity, C-reactive protein, and blood leukocytes. Inflamm Bowel Dis 2009;15:1851–1858.PMID: 19462421.Article PubMed
33. Schreiber S, Nikolaus S, Hampe J. Activation of nuclear factor kappa B inflammatory bowel disease. Gut 1998;42:477–484.PMID: 9616307.Article PubMed PMC
34. Chaparro M, Ordás I, Cabré E, et al. Safety of thiopurine therapy in inflammatory bowel disease: long-term follow-up study of 3931 patients. Inflamm Bowel Dis 2013;19:1404–1410.PMID: 23665964.Article PubMed
35. Qasim A, McDonald S, Sebastian S, et al. Efficacy and safety of 6-thioguanine in the management of inflammatory bowel disease. Scand J Gastroenterol 2007;42:194–199.PMID: 17327939.Article PubMed
36. Khan N, Abbas AM, Lichtenstein GR, Loftus EV Jr, Bazzano LA. Risk of lymphoma in patients with ulcerative colitis treated with thiopurines: a nationwide retrospective cohort study. Gastroenterology 2013;145:1007–1015.PMID: 23891975.Article PubMed
37. Beaugerie L, Brousse N, Bouvier AM, et al. Lymphoproliferative disorders in patients receiving thiopurines for inflammatory bowel disease: a prospective observational cohort study. Lancet 2009;374:1617–1625.PMID: 19837455.Article PubMed
38. Travis SP, Stange EF, Lémann M, et al. European evidence-based consensus on the management of ulcerative colitis: current management. J Crohns Colitis 2008;2:24–62.PMID: 21172195.Article PubMed PDF
39. Roblin X, Peyrin-Biroulet L, Phelip JM, Nancey S, Flourie B. A 6-thioguanine nucleotide threshold level of 400 pmol/8 x 10(8) erythrocytes predicts azathioprine refractoriness in patients with inflammatory bowel disease and normal TPMT activity. Am J Gastroenterol 2008;103:3115–3122.PMID: 19086961.Article PubMed

Fig. 1

Flow chart and cumurative remission maintenance and colectomy-free rate. (A) Clinical course of the patients with UC who were enrolled in this study. Of the 87 patients with UC who received various induction therapies, including 5-aminosalicylate (5-ASA), granulocyte-monocyte adsorption apheresis (GMAA), corticosteroids, and calcineurin inhibitors, 68 (78.2%) achieved a clinical response with induction treatment and thiopurine. Fifty-nine patients (67.8%) achieved clinical remission with thiopurine and 5-ASA after tapering the dose in the induction treatment, and 56 patients (64.4%) continued maintenance treatment with thiopurine. (B) Cumulative remission-maintenance rate. The cumulative remission-maintenance rate in 59 patients treated with thiopurine and 5-ASA after tapering the dose in the induction treatment was estimated to be 43.9% at 84 months. (C) Survival. The cumulative colectomy-free survival rate in the UC patients whose remission was maintained with thiopurine and 5-ASA was estimated to be 88.0% at 84 months.

Table 1

Demographic and Clinical Characteristics of the Patients With UC and the Patients in the Remission and Relapse Groups Treated With Thiopurine and 5-Aminosalicylate (5-ASA)

	All (n=56)	Remission group (n=37)	Relapse group (n=19)	P-value
Sex (men/women)	38 (67.9)/18 (32.2)	25 (67.6)/12 (32.4)	13 (68.4)/6 (31.6)	0.940
Age (yr)	31.5 (13.0-83.0)	36.0 (13.0-83.0)	26.0 (18.0-56.0)	0.070
Disease duration (mo)^*	33.5 (1.0-292.0)	40.0 (1.0-292.0)	15.0 (1.0-110.0)	0.080
Modified Truelove and Witts Severity Index^*	5.0 (1.0-13.0)	5.0 (1.0-13.0)	5.0 (2.0-10.0)	1.000
Mayo score (endoscopy)^*	2.0 (1.0-3.0)	2.0 (1.0-3.0)	3.0 (1.0-3.0)	0.340
Extent of disease
Proctitis	3 (5.4)	3 (8.1)	0 (0.0)	0.240
Left-side type	16 (28.6)	14 (37.8)	2 (10.5)	0.070
Extensive colitis	37 (66.0)	20 (54.1)	17 (89.5)	0.020
Refractory UC	39 (69.6)	25 (64.1)	14 (82.4)	0.170
Induction treatment
Concomitant use of 5-ASA	52 (94.5)	35 (94.6)	17 (89.5)	0.480
GMAA	4 (7.1)	2 (5.1)	2 (11.8)	0.380
Corticosteroids	26 (46.4)	14 (35.9)	12 (70.6)	0.020
Calcineurin-inhibitor	14 (25.0)	10 (25.6)	4 (23.5)	0.910
History of treatment with a corticosteroid dosage ≥40 mg/day	20 (35.7)	8 (20.5)	12 (70.6)	<0.001
Laboratory examination
White blood cell count (/µL)	6,500 (4,100-14,600)	6,450 (4,100-13,100)	6,950 (5,200-14,600)	0.580
Hemoglobin level (g/dL)	12.1 (8.2-15.2)	12.0 (8.2-14.8)	12.6 (9.2-15.2)	0.590
MCV delta values for 3 months after initiating thiopurines (fL)	2.5 (-6.9 to 14.8)	2.8 (-6.9 to 14.8)	0.8 (-6.9 to 9.1)	0.240
CRP concentration (mg/dL)	0.3 (0.0-3.3)	0.3 (0-3.3)	0.3 (0.0-1.0)	0.480

The numbers of patients are shown, and the % values are percentages of the total available data.

^*Data are presented as median (range). The P-value was evaluated between the remission and relapse groups.

GMAA, granulocyte-monocyte adsorption apheresis; MCV, mean corpuscular volume.

Table 2

Predictive Factors of Remission Maintenance With Thiopurine and 5-Aminosalicylate Treatment

	Hazard ratio	95% CI	P-value
Age	1.02	0.98-1.06	0.90
Disease duration	0.99	0.98-1.00	0.98
Left-sided colitis	0.24	0.05-1.11	0.07
Induction treatment with corticosteroids	0.72	0.25-2.09	0.54
No history of treatment with a corticosteroid dosage ≥40 mg/day	3.76	1.30-10.88	0.01

Every item was evaluated at the time thiopurine treatment was initiated.

Table 3

Demographic and Clinical Characteristics of the Patients With UC Treated With Thiopurine and 5-Aminosalicylate (5-ASA) in the Mucosal Healing and Non-Mucosal Healing Groups

	Mucosal healing (n=23)	Non-mucosal healing (n=15)	P-value
Sex (men/women)	16 (69.6)/7 (30.4)	10 (66.7)/5 (33.3)	0.85
Age (yr)	41.0 (18.0-83.0)	28.0 (20-58)	0.07
Disease duration (mo)^*	28.0 (1.0-151.0)	63.0 (1.0-292.0)	0.24
Modified Truelove and Witts Severity Index^*	5.0 (1.0-10.0)	5.0 (1.0-13.0)	0.85
Mayo score (endoscopy)^*	3.0 (1.0-3.0)	2.0 (1.0-3.0)	0.89
Extent of disease
Proctitis	1 (4.4)	1 (6.7)	0.75
Left sided type	5 (21.7)	5 (33.3)	0.43
Extensive colitis	17 (73.9)	9 (60.0)	0.37
Refractory UC	17 (73.9)	9 (60.0)	0.37
Induction treatment
5-ASA	22 (95.7)	14 (93.3)	0.75
GMAA	2 (8.7)	0 (0.0)	0.24
Corticosteroids	7 (56.5)	10 (66.6)	0.55
Calcineurin-inhibitor	6 (2.6)	4 (26.7)	0.63
History of treatment with a corticosteroid dosage ≥40 mg/day	7 (56.5)	8 (80.0)	0.16
Laboratory examination
White blood cell count (/µL)	6,450 (4,000-14,600)	7,300 (4,500-13,100)	0.66
Hemoglobin level (g/dL)	12.3 (8.2-14.8)	12.2 (9.0-15.2)	0.85
MCV delta values 3 months after initiating thiopurines (fL)	3.0 (-6.9 to 12.3)	2.6 (-6.9 to 9.0)	0.34
CRP concentration (mg/dL)	0.5 (0.1-2.3)	1.1 (0.0-6.6)	0.12

The numbers of patients are shown, and the % values are percentages of the total available data.

^*Data are presented as mean ± standard deviation values.

GMAA, granulocyte-monocyte adsorption apheresis; MCV, mean corpuscular volume.

Table 4

Predictive Alaility of Mucosal Healing With Thiopurine and 5-Aminosalicylate Treatment

	Hazard ratio	95% CI	P-value
Age	0.99	0.93-1.04	0.63
Disease duration	1.01	0.99-1.02	0.83
Induction treatment with corticosteroids	3.28	0.80-13.40	0.99
No history of treatment with a corticosteroid dosage ≥40 mg/day	3.81	0.88-16.42	0.07
Serum CRP	1.46	1.03-2.06	0.03

Every item was evaluated at the time thiopurine treatment was initiated.

Table 5

Adverse Events During the Study Period According to Treatment With Thiopurine and 5-Aminosalicylate

	Adverse events
Death	0
Infections
Pneumonia	1
Infectious mononucleosis	1
Gastroenterology and hepatology
Nausea	4
Liver dysfunction	4
Pancreatitis	1
Hematology
Leukopenia	3
Anemia	2
Dermatology
Depilation	1
Total events	17 (28.8)

The numbers of adverse events are shown, not the numbers of patients, and % values are percentage of total of available data.

Figure & Data

REFERENCES

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Efficacy and Safety of Long-Term Thiopurine Maintenance Treatment in Japanese Patients With Ulcerative Colitis

Intest Res. 2015;13(3):250-258. Published online June 9, 2015

DOI: https://doi.org/10.5217/ir.2015.13.3.250

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Efficacy and Safety of Long-Term Thiopurine Maintenance Treatment in Japanese Patients With Ulcerative Colitis

Fig. 1 Flow chart and cumurative remission maintenance and colectomy-free rate. (A) Clinical course of the patients with UC who were enrolled in this study. Of the 87 patients with UC who received various induction therapies, including 5-aminosalicylate (5-ASA), granulocyte-monocyte adsorption apheresis (GMAA), corticosteroids, and calcineurin inhibitors, 68 (78.2%) achieved a clinical response with induction treatment and thiopurine. Fifty-nine patients (67.8%) achieved clinical remission with thiopurine and 5-ASA after tapering the dose in the induction treatment, and 56 patients (64.4%) continued maintenance treatment with thiopurine. (B) Cumulative remission-maintenance rate. The cumulative remission-maintenance rate in 59 patients treated with thiopurine and 5-ASA after tapering the dose in the induction treatment was estimated to be 43.9% at 84 months. (C) Survival. The cumulative colectomy-free survival rate in the UC patients whose remission was maintained with thiopurine and 5-ASA was estimated to be 88.0% at 84 months.

Fig. 1

Efficacy and Safety of Long-Term Thiopurine Maintenance Treatment in Japanese Patients With Ulcerative Colitis

Supplemental Table 1

Modified Truelove and Witts Severity Index Score

Score	0	1	2	3	4	5
Bowel movement	0-2	3-4	5-6	7-9	≤10
Nocturnal diarrhea	No	Yes
Visible blood in stool (%)	0	<50	≤50	100
Abdominal tenderness	None	Mild	Moderate	Severe
Abdominal pain/cramping	None	Mild	Moderate	Severe
Need for antidiarrheals	No	Yes
General status	Perfect	Very good	Good	Average	Poor	Terrible
Fecal incontinence	No	Yes

Severe disease, ≤12; mild to moderate, 5-11; remission category, ≤4

Table 1

Demographic and Clinical Characteristics of the Patients With UC and the Patients in the Remission and Relapse Groups Treated With Thiopurine and 5-Aminosalicylate (5-ASA)

	All (n=56)	Remission group (n=37)	Relapse group (n=19)	P-value
Sex (men/women)	38 (67.9)/18 (32.2)	25 (67.6)/12 (32.4)	13 (68.4)/6 (31.6)	0.940
Age (yr)	31.5 (13.0-83.0)	36.0 (13.0-83.0)	26.0 (18.0-56.0)	0.070
Disease duration (mo)^*	33.5 (1.0-292.0)	40.0 (1.0-292.0)	15.0 (1.0-110.0)	0.080
Modified Truelove and Witts Severity Index^*	5.0 (1.0-13.0)	5.0 (1.0-13.0)	5.0 (2.0-10.0)	1.000
Mayo score (endoscopy)^*	2.0 (1.0-3.0)	2.0 (1.0-3.0)	3.0 (1.0-3.0)	0.340
Extent of disease
Proctitis	3 (5.4)	3 (8.1)	0 (0.0)	0.240
Left-side type	16 (28.6)	14 (37.8)	2 (10.5)	0.070
Extensive colitis	37 (66.0)	20 (54.1)	17 (89.5)	0.020
Refractory UC	39 (69.6)	25 (64.1)	14 (82.4)	0.170
Induction treatment
Concomitant use of 5-ASA	52 (94.5)	35 (94.6)	17 (89.5)	0.480
GMAA	4 (7.1)	2 (5.1)	2 (11.8)	0.380
Corticosteroids	26 (46.4)	14 (35.9)	12 (70.6)	0.020
Calcineurin-inhibitor	14 (25.0)	10 (25.6)	4 (23.5)	0.910
History of treatment with a corticosteroid dosage ≥40 mg/day	20 (35.7)	8 (20.5)	12 (70.6)	<0.001
Laboratory examination
White blood cell count (/µL)	6,500 (4,100-14,600)	6,450 (4,100-13,100)	6,950 (5,200-14,600)	0.580
Hemoglobin level (g/dL)	12.1 (8.2-15.2)	12.0 (8.2-14.8)	12.6 (9.2-15.2)	0.590
MCV delta values for 3 months after initiating thiopurines (fL)	2.5 (-6.9 to 14.8)	2.8 (-6.9 to 14.8)	0.8 (-6.9 to 9.1)	0.240
CRP concentration (mg/dL)	0.3 (0.0-3.3)	0.3 (0-3.3)	0.3 (0.0-1.0)	0.480

The numbers of patients are shown, and the % values are percentages of the total available data.

^*Data are presented as median (range). The P-value was evaluated between the remission and relapse groups.

GMAA, granulocyte-monocyte adsorption apheresis; MCV, mean corpuscular volume.

Table 2

Predictive Factors of Remission Maintenance With Thiopurine and 5-Aminosalicylate Treatment

	Hazard ratio	95% CI	P-value
Age	1.02	0.98-1.06	0.90
Disease duration	0.99	0.98-1.00	0.98
Left-sided colitis	0.24	0.05-1.11	0.07
Induction treatment with corticosteroids	0.72	0.25-2.09	0.54
No history of treatment with a corticosteroid dosage ≥40 mg/day	3.76	1.30-10.88	0.01

Every item was evaluated at the time thiopurine treatment was initiated.

Table 3

Demographic and Clinical Characteristics of the Patients With UC Treated With Thiopurine and 5-Aminosalicylate (5-ASA) in the Mucosal Healing and Non-Mucosal Healing Groups

	Mucosal healing (n=23)	Non-mucosal healing (n=15)	P-value
Sex (men/women)	16 (69.6)/7 (30.4)	10 (66.7)/5 (33.3)	0.85
Age (yr)	41.0 (18.0-83.0)	28.0 (20-58)	0.07
Disease duration (mo)^*	28.0 (1.0-151.0)	63.0 (1.0-292.0)	0.24
Modified Truelove and Witts Severity Index^*	5.0 (1.0-10.0)	5.0 (1.0-13.0)	0.85
Mayo score (endoscopy)^*	3.0 (1.0-3.0)	2.0 (1.0-3.0)	0.89
Extent of disease
Proctitis	1 (4.4)	1 (6.7)	0.75
Left sided type	5 (21.7)	5 (33.3)	0.43
Extensive colitis	17 (73.9)	9 (60.0)	0.37
Refractory UC	17 (73.9)	9 (60.0)	0.37
Induction treatment
5-ASA	22 (95.7)	14 (93.3)	0.75
GMAA	2 (8.7)	0 (0.0)	0.24
Corticosteroids	7 (56.5)	10 (66.6)	0.55
Calcineurin-inhibitor	6 (2.6)	4 (26.7)	0.63
History of treatment with a corticosteroid dosage ≥40 mg/day	7 (56.5)	8 (80.0)	0.16
Laboratory examination
White blood cell count (/µL)	6,450 (4,000-14,600)	7,300 (4,500-13,100)	0.66
Hemoglobin level (g/dL)	12.3 (8.2-14.8)	12.2 (9.0-15.2)	0.85
MCV delta values 3 months after initiating thiopurines (fL)	3.0 (-6.9 to 12.3)	2.6 (-6.9 to 9.0)	0.34
CRP concentration (mg/dL)	0.5 (0.1-2.3)	1.1 (0.0-6.6)	0.12

The numbers of patients are shown, and the % values are percentages of the total available data.

^*Data are presented as mean ± standard deviation values.

GMAA, granulocyte-monocyte adsorption apheresis; MCV, mean corpuscular volume.

Table 4

Predictive Alaility of Mucosal Healing With Thiopurine and 5-Aminosalicylate Treatment

	Hazard ratio	95% CI	P-value
Age	0.99	0.93-1.04	0.63
Disease duration	1.01	0.99-1.02	0.83
Induction treatment with corticosteroids	3.28	0.80-13.40	0.99
No history of treatment with a corticosteroid dosage ≥40 mg/day	3.81	0.88-16.42	0.07
Serum CRP	1.46	1.03-2.06	0.03

Every item was evaluated at the time thiopurine treatment was initiated.

Table 5

Adverse Events During the Study Period According to Treatment With Thiopurine and 5-Aminosalicylate

	Adverse events
Death	0
Infections
Pneumonia	1
Infectious mononucleosis	1
Gastroenterology and hepatology
Nausea	4
Liver dysfunction	4
Pancreatitis	1
Hematology
Leukopenia	3
Anemia	2
Dermatology
Depilation	1
Total events	17 (28.8)

The numbers of adverse events are shown, not the numbers of patients, and % values are percentage of total of available data.

Supplemental Table 1 Modified Truelove and Witts Severity Index Score

Severe disease, ≤12; mild to moderate, 5-11; remission category, ≤4

Table 1 Demographic and Clinical Characteristics of the Patients With UC and the Patients in the Remission and Relapse Groups Treated With Thiopurine and 5-Aminosalicylate (5-ASA)

The numbers of patients are shown, and the % values are percentages of the total available data.

^*Data are presented as median (range). The P-value was evaluated between the remission and relapse groups.

GMAA, granulocyte-monocyte adsorption apheresis; MCV, mean corpuscular volume.

Table 2 Predictive Factors of Remission Maintenance With Thiopurine and 5-Aminosalicylate Treatment

Every item was evaluated at the time thiopurine treatment was initiated.

Table 3 Demographic and Clinical Characteristics of the Patients With UC Treated With Thiopurine and 5-Aminosalicylate (5-ASA) in the Mucosal Healing and Non-Mucosal Healing Groups

The numbers of patients are shown, and the % values are percentages of the total available data.

^*Data are presented as mean ± standard deviation values.

GMAA, granulocyte-monocyte adsorption apheresis; MCV, mean corpuscular volume.

Table 4 Predictive Alaility of Mucosal Healing With Thiopurine and 5-Aminosalicylate Treatment

Every item was evaluated at the time thiopurine treatment was initiated.

Table 5 Adverse Events During the Study Period According to Treatment With Thiopurine and 5-Aminosalicylate

The numbers of adverse events are shown, not the numbers of patients, and % values are percentage of total of available data.