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Vulnerable patients: burning questions in IBD

Written by | 30 Mar 2017 | All Medical News

An interesting session at ECCO dealt with the patients for whom there is sparce data to guide their treatment – experts in the field gave their guidance to delegates. Professor Jean-Frederic Colombel (New York, USA) comments on his practice in the elderly IBD patient.

Although the therapeutic arsenal for treating IBD is greater and more sophisticated than ever in 2017, there remain large groups of patients who present particular challenges for gastroenterologists in their everyday practice. One of the scientific sessions at the 12th Congress of ECCO was dedicated to the management of vulnerable patients, including pregnant women, elderly patients and patients diagnosed with cancer.

Pregnancy

Professor Janneke van der Woude described the pregnancy policy at the Erasmus Medical Centre in Rotterdam, under which all female IBD patients planning a pregnancy receive counselling, and disease remission is ideally achieved before conception. During the pregnancy the patient receives low-risk therapy to maintain remission; any relapse during pregnancy is treated without delay and an overall objective is to limit foetal drug exposure to the greatest possible extent. The risk of miscarriage or severe congenital malformations due to drug exposure is greatest during the first trimester; during later stages of the pregnancy the risk of birth defects is reduced but altered function or growth of normal organs may still occur.

Since the introduction of anti-TNF therapy in the late 1990s clinical experience has shown that use of anti-TNFs during pregnancy is associated with normal fertility and no increased risk of miscarriages during the first trimester, and no signs of an increased risk of birth defects.1-4 A protocol of stopping therapy at week 22-24 of pregnancy to limit foetal exposure to anti-TNF showed no increased risk of relapse in women in sustained remission.5, 6 Although exposure to anti-TNF during pregnancy has not been linked to adverse outcomes, there have been case reports of adverse outcomes after live vaccination of the new-born child7 and of neonatal neutropenia.8 Based on the available clinical experience, the policy at Erasmus MC is to stop infliximab treatment in week 22 and adalimumab in week 33 in women in sustained remission only.

Experience with vedolizumab is limited and no firm recommendations can be given. The effect of vedolizumab on fertility is unknown, but MAdCAM-1 is expressed in the placenta during the first trimester.9 There have been 81 pregnancies and 11 spontaneous abortions entered in the post-marketing registry for vedolizumab.10 Likewise the risks of congenital malformations and infections in exposed newborns are unknown. The policy at Erasmus MC is to not initiate vedolizumab in IBD patients planning a pregnancy. If there are no alternative treatments the patient will be offered counselling, and if she agrees and remains in sustained remission vedolizumab will be continued until week 22 of pregnancy.

Elderly patients

In a talk on managing elderly patients with IBD, Professor Jean-Frédéric Colombel, from Mount Sinai in New York, pointed out the difficulty of making recommendations in this group – not least due to the lack of an agreed definition of ‘elderly’ and the fact that elderly patients typically will be excluded from randomised clinical trials. That said, there is clear evidence that azathioprine should be avoided in elderly patients due to the risk of cancers. A prospective cohort study in nearly 20,000 IBD patients showed that amongst patients aged over 65 years, the incidence rate of lymphoma was more than three times higher in patients on thiopurines compared with those who had never been exposed to thiopurines.11 Similarly, patients over 65 years with thiopurine exposure also have significantly higher rates of non-melanoma skin cancer12 and urinary tract cancer.13 Combination therapy with infliximab tilts the benefit-risk-balance even further against the use of thiopurines beyond the age of around 55 years.14

 

Less clear-cut is the question of whether elderly IBD patients should have different types of surgery. Elderly patients tend to cope less well with hospitalisation in terms of mortality and morbidity, especially following emergency surgery and elective surgery should therefore be preferred in this patient group.15, 16 Data on IBD patients undergoing restorative proctocolectomy shows that although elderly patients tend to stay longer in hospital and have more serious complications, their overall rates of complications and pouch failure were not different from younger patients.17 Such data highlights the need for a definition that focuses not on the age of patients but on their level of frailty, so that more specific recommendations can be made for vulnerable patients regardless of age.

Patients with cancer

The need for life-long immunosuppressive therapy to maintain remission in IBD poses a considerable challenge in patients who develop cancer. Although not much data has been published, there is general agreement that immunosuppressive therapy should be stopped in patients with newly-diagnosed cancer until the cancer is under control, except in cases of non-aggressive basal cell carcinoma.18, 19 If this is not possible, due to metastatic cancer or active IBD, quality of life should be prioritised and treatment with anti-TNF considered as published data has shown these to be well tolerated without worsening cancer progression.20, 21 In IBD patients with a history of cancer it is important to consider both the risk of new, second cancers and recurrence of cancer. Although a recent meta-analysis showed no increase in the rate of new and recurrent cancers in previous cancer patients who received anti-TNF therapy, immune modulators, or combination therapy22 it is still advisable to proceed with caution and consider the impact of impairing immune surveillance mechanisms in cancers with a lifelong risk of recurrence, such as some melanomas and breast cancers.23 The 2016 ECCO guidelines state that immunosuppressive therapy for IBD should be delayed for up to 5 years after cancer treatment19 except in patients with severe IBD with no therapeutic alternative. All treatment decisions should be made in consultation with an oncologist.

References

 

  1. Winger EE, Reed JL. Treatment with tumor necrosis factor inhibitors and intravenous immunoglobulin improves live birth rates in women with recurrent spontaneous abortion. Am J Reprod Immunol 2008;60:8-16.
  2. Prokesch A, Blaschitz A, Bauer T, et al. Placental DAPK1 and autophagy marker LC3B-II are dysregulated by TNF-α in a gestational age-dependent manner. Histochemistry and Cell Biology 2017:1-11.
  3. Broms G, Granath F, Ekbom A, et al. Low Risk of Birth Defects for Infants Whose Mothers Are Treated With Anti-Tumor Necrosis Factor Agents During Pregnancy. Clin Gastroenterol Hepatol 2016;14:234-41 e1-5.
  4. Shihab Z, Yeomans ND, De Cruz P. Anti-Tumour Necrosis Factor alpha Therapies and Inflammatory Bowel Disease Pregnancy Outcomes: A Meta-analysis. J Crohns Colitis 2016;10:979-88.
  5. de Lima A, Zelinkova Z, van der Ent C, et al. Tailored anti-TNF therapy during pregnancy in patients with IBD: maternal and fetal safety. Gut 2016;65:1261-8.
  6. Julsgaard M, Christensen LA, Gibson PR, et al. Concentrations of Adalimumab and Infliximab in Mothers and Newborns, and Effects on Infection. Gastroenterology 2016;151:110-9.
  7. Cheent K, Nolan J, Shariq S, et al. Case Report: Fatal case of disseminated BCG infection in an infant born to a mother taking infliximab for Crohn’s disease. J Crohns Colitis 2010;4:603-5.
  8. Guiddir T, Fremond ML, Triki TB, et al. Anti-TNF-alpha therapy may cause neonatal neutropenia. Pediatrics 2014;134:e1189-93.
  9. Zamborsky T, Berakova K, Kadleckova B, et al. P339 MadCAM1 expression in intestinal lamina propria endothelium varies among inflammatory bowel disease patients. Journal of Crohn’s and Colitis 2017;11:S249-S249.
  10. Mahadevan U, Vermeire S, Lasch K, et al. Vedolizumab exposure in pregnancy: outcomes from clinical studies in inflammatory bowel disease. Aliment Pharmacol Ther 2017.
  11. 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;374:1617-25.
  12. Peyrin-Biroulet L, Khosrotehrani K, Carrat F, et al. Increased risk for nonmelanoma skin cancers in patients who receive thiopurines for inflammatory bowel disease. Gastroenterology 2011;141:1621-28 e1-5.
  13. Bourrier A, Carrat F, Colombel JF, et al. Excess risk of urinary tract cancers in patients receiving thiopurines for inflammatory bowel disease: a prospective observational cohort study. Aliment Pharmacol Ther 2016;43:252-61.
  14. Scott FI, Vajravelu RK, Bewtra M, et al. The benefit-to-risk balance of combining infliximab with azathioprine varies with age: a markov model. Clin Gastroenterol Hepatol 2015;13:302-309 e11.
  15. Ikeuchi H, Uchino M, Matsuoka H, et al. Prognosis following emergency surgery for ulcerative colitis in elderly patients. Surg Today 2014;44:39-43.
  16. Ananthakrishnan AN, McGinley EL, Binion DG. Inflammatory bowel disease in the elderly is associated with worse outcomes: a national study of hospitalizations. Inflamm Bowel Dis 2009;15:182-9.
  17. Colombo F, Sahami S, de Buck Van Overstraeten A, et al. Restorative Proctocolectomy in Elderly IBD Patients: A Multicentre Comparative Study on Safety and Efficacy. J Crohns Colitis 2016.
  18. Bernheim O, Colombel JF, Ullman TA, et al. The management of immunosuppression in patients with inflammatory bowel disease and cancer. Gut 2013;62:1523-8.
  19. Annese V, Beaugerie L, Egan L, et al. European Evidence-based Consensus: Inflammatory Bowel Disease and Malignancies. J Crohns Colitis 2015;9:945-65.
  20. Brown ER, Charles KA, Hoare SA, et al. A clinical study assessing the tolerability and biological effects of infliximab, a TNF-alpha inhibitor, in patients with advanced cancer. Ann Oncol 2008;19:1340-6.
  21. Wiedenmann B, Malfertheiner P, Friess H, et al. A multicenter, phase II study of infliximab plus gemcitabine in pancreatic cancer cachexia. J Support Oncol 2008;6:18-25.
  22. Shelton E, Laharie D, Scott FI, et al. Cancer Recurrence Following Immune-Suppressive Therapies in Patients With Immune-Mediated Diseases: A Systematic Review and Meta-analysis. Gastroenterology 2016;151:97-109 e4.
  23. Sosa MS, Bragado P, Aguirre-Ghiso JA. Mechanisms of disseminated cancer cell dormancy: an awakening field. Nat Rev Cancer 2014;14:611-22.
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