Journals | Policy | Permission

Gastroenterology Research

Case Report

Volume 7, Number 1, February 2014, pages 28-31

Infectious Colitis Associated With Ipilimumab Therapy

The incidence of malignant melanoma is currently on the rise accounting for the majority of deaths caused by cancers originating from the skin [1]. While metastatic melanoma is a devastating disease, there are a few therapies that can improve survival. Ipilimumab is a monoclonal antibody against cytotoxic T lymphocyte-associated molecule-4 (CTLA-4), which is a strong negative regulator of T cell activation [2]. Ipilimumab is thought to promote anti-tumor activity by enhancing cell mediated immunity and has been shown to improve overall survival in both previously treated and treatment naive patients [3, 4]. Given the drug’s mechanism of action, it is no surprise that treatment with ipilimumab has resulted in significant immune-related adverse events (IRAEs) [5, 6]. In a clinical trial by Hodi et al [3], the incidence of overall IRAEs was reported to be approximately 60% with diarrhea being the most common. Severe immune-mediated enterocolitis occurred in 7% of patients (defined as diarrhea of ≥ 7 stools above baseline, fever, ileus, or peritoneal signs; Grade 3-5) [3]. There are suggestions that increasing doses of ipilimumab may increase the incidence of IRAEs, with grade 3 or 4 diarrhea reported in 18% of patients receiving 10 mg/kg of ipilimumab [7]. Most gastrointestinal IRAEs are reversible with the use of immunosuppressive therapies, but some may result in severe and life threatening events necessitating long term immunosuppression and permanent discontinuation of therapy. Current clinical guidelines also advise to rule out infectious etiologies in patients with gastrointestinal symptoms. We present a case of immune-related severe colitis associated with infectious diarrhea in a patient receiving ipilimumab therapy for metastatic melanoma.

Our patient is a 22-year-old female with Stage IVA melanoma (BRAF, c-KIT and NRAS negative) of the left arm who is status post resection with positive surgical margins. She underwent local radiation and received immunotherapy with ipilimumab 3 mg/kg every three weeks. She completed three doses of ipilimumab with a rash being her most significant IRAE. The patient presented for admission to our hospital with a one-day history of fever (102.5 F), 10 episodes of large volume watery diarrhea, and mild abdominal discomfort. She gave a history of recent travel to a wedding and noted that two other guests in attendance had also developed diarrheal illnesses. Stool studies were sent for Clostridium difficile, bacterial cultures, and ova and parasites. An upright chest film did not reveal any free air under the diaphragm. Ipilimumab was discontinued and high dose prednisone (1 mg/kg once a day) started. Colonoscopy revealed a grossly normal terminal ileum, mild diffuse right-sided colitis with erythema, moderate diffuse mid-colon inflammation without ulceration, and patchy moderate to severe left-colon inflammation without ulceration that was contiguous with the anal canal (Fig. 1A-D). Colonic biopsies were obtained and revealed an intact crypt architecture with an increased inflammatory cell infiltrate in the lamina propria, neutrophilic cryptitis, crypt abscesses, and surface epithelial injury (Fig. 2A, B). Given the clinical setting, these histopathologic features were consistent with ipilimumab-induced colitis. Immunohistochemical staining for Cytomegalovirus was negative. Stool testing was negative for Clostridium difficile and ova and parasites. After three days of high dose steroids she continued to have 5 stools per day and her prednisone was increased to 1mg/kg twice a day. On day 4 of her hospitalization, her stool culture was positive for Salmonella enteritides and she was started on ciprofloxacin with clinical improvement. She was discharged home on high dose prednisone (1 mg/kg twice a day) with a prolonged taper and a 14-day course of ciprofloxacin. Because her presentation met criteria for severe colitis, ipilimumab was permanently discontinued. At her two-month follow-up, the patient had completed a prolonged steroid taper and reported no further diarrhea. Her most recent Computerized tomography scan revealed multiple new sub-centimeter bilateral pulmonary nodules suspicious for metastatic disease. The remainder of her oncologic treatment course is yet to be determined.

Click for large image

Figure 1. Colonoscopy revealed a grossly normal terminal ileum, mild diffuse right-sided colitis, moderate diffuse mid-colon colitis, and patchy moderate to severe left-sided colitis that was contiguous with the anal canal.

Click for large image

Figure 2. Colonic biopsies were obtained and revealed an intact crypt architecture (A, 200× magnification) with an increased inflammatory cell infiltrate in the lamina propria, neutrophilic cryptitis, crypt abscesses, and surface epithelial injury (B, 400× magnification; arrow highlights crypt abscess).

Although ipilimumab is an innovative tool in the treatment of melanoma, the high incidence of IRAEs often limits its use. Kahler and Hauschild report that 84.6% of patients receiving ipilimumab at a dose of 10 mg/kg had drug related side effects with gastrointestinal tract, liver and skin being the most common organs experiencing severe effects [8]. Treatment of severe immune-related enterocolitis requires cessation of ipilimumab and administration of steroids, usually over a prolonged taper of at least one month [7]. If clinically warranted, gastrointestinal perforation should be ruled out. In the setting of refractory colitis, second line therapy involves the use of the anti-TNF monoclonal antibody infliximab. Given the frequency, severity and necessity to discontinue ipilimumab therapy after severe gastrointestinal toxicity, we have a great interest in understanding the pathophysiology of immune-mediated colitis, as well as in developing strategies to manage and prevent this phenomenon.

As of yet, no prophylactic therapies for immune-related enterocolitis have been proven successful. Prophylactic budesonide therapy was evaluated, but not beneficial in reducing the incidence of grade 2 or higher diarrhea [9]. The pathophysiology of immune-related diarrhea is complex with prior studies investigating altered regulation of gastrointestinal mucosal immunity and altered antibody levels to enteric flora in the setting of immune modulating therapy. Although there has been suggestion of many similarities between ipilimumab-induced gastrointestinal toxicity and inflammatory bowel disease, these conditions differ in antibody levels to enteric flora, histologic features and the location of inflammation [10]. It has also been hypothesized that blockade of CTLA-4 can result in depletion of FOXP3+ regulatory T cells, which might explain the mechanism behind immune-mediated enterocolitis [11]. Increased expression of neutrophil activation markers, such as CD177 and CEACAM1, has been associated with risk of gastrointestinal IRAEs in patients receiving ipilimumab. Due to low sensitivity these biomarkers were not felt to be useful for clinical decision making [12].

Gastrointestinal toxicity symptoms often overlap with infectious symptoms and it is still unclear if infectious or enteric flora plays a role in triggering immune-mediated colitis. In our reported case, an infectious pathogen was identified with temporal relationship to symptoms and could be suggestive of a causal relationship. Based on this observation, it may be hypothesized that the use of prophylactic antibiotics could potentially have a preventive effect on the incidence of gastrointestinal IRAEs in patients receiving ipilimumab with hopes of improving the safety profile of ipilimumab. Additional evaluation of the underlying mechanism is necessary to reduce the incidence of drug associated toxicities.

1. Agarwala SS, O'Day SJ. Current and future adjuvant immunotherapies for melanoma: blockade of cytotoxic T-lymphocyte antigen-4 as a novel approach. Cancer Treat Rev. 2011;37(2):133-142.
   doi pubmed
2. McCoy KD, Le Gros G. The role of CTLA-4 in the regulation of T cell immune responses. Immunol Cell Biol. 1999;77(1):1-10.
   doi pubmed
3. Hodi FS, O'Day SJ, McDermott DF, Weber RW, Sosman JA, Haanen JB, Gonzalez R, et al. Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med. 2010;363(8):711-723.
   doi pubmed
4. Robert C, Thomas L, Bondarenko I, O'Day S, M DJ, Garbe C, Lebbe C, et al. Ipilimumab plus dacarbazine for previously untreated metastatic melanoma. N Engl J Med. 2011;364(26):2517-2526.
   doi pubmed
5. Beck KE, Blansfield JA, Tran KQ, Feldman AL, Hughes MS, Royal RE, Kammula US, et al. Enterocolitis in patients with cancer after antibody blockade of cytotoxic T-lymphocyte-associated antigen 4. J Clin Oncol. 2006;24(15):2283-2289.
   doi pubmed
6. Culos KA, Cuellar S. Novel targets in the treatment of advanced melanoma: new first-line treatment options. Ann Pharmacother. 2013;47(4):519-526.
   doi pubmed
7. Weber JS, Kahler KC, Hauschild A. Management of immune-related adverse events and kinetics of response with ipilimumab. J Clin Oncol. 2012;30(21):2691-2697.
   doi pubmed
8. Kahler KC, Hauschild A. Treatment and side effect management of CTLA-4 antibody therapy in metastatic melanoma. J Dtsch Dermatol Ges. 2011;9(4):277-286.
   doi pubmed
9. Weber J, Thompson JA, Hamid O, Minor D, Amin A, Ron I, Ridolfi R, et al. A randomized, double-blind, placebo-controlled, phase II study comparing the tolerability and efficacy of ipilimumab administered with or without prophylactic budesonide in patients with unresectable stage III or IV melanoma. Clin Cancer Res. 2009;15(17):5591-5598.
   doi pubmed
10. Berman D, Parker SM, Siegel J, Chasalow SD, Weber J, Galbraith S, Targan SR, et al. Blockade of cytotoxic T-lymphocyte antigen-4 by ipilimumab results in dysregulation of gastrointestinal immunity in patients with advanced melanoma. Cancer Immun. 2010;10:11.
    pubmed
11. Nancey S, Boschetti G, Cotte E, Ruel K, Almeras T, Chauvenet M, Stroeymeyt K, et al. Blockade of cytotoxic T-lymphocyte antigen-4 by ipilimumab is associated with a profound long-lasting depletion of Foxp3+ regulatory T cells: a mechanistic explanation for ipilimumab-induced severe enterocolitis?. Inflamm Bowel Dis. 2012;18(8):E1598-1600.
    doi pubmed
12. Shahabi V, Berman D, Chasalow SD, Wang L, Tsuchihashi Z, Hu B, Panting L, et al. Gene expression profiling of whole blood in ipilimumab-treated patients for identification of potential biomarkers of immune-related gastrointestinal adverse events. J Transl Med. 2013;11(1):75.
    doi pubmed

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Gastroenterology Research is published by Elmer Press Inc.