Volume 36, Issue 5 pp. 632-636
Original Articles

A Prospective Study of the Efficacy and Tolerance of a Chimeric Antibody to Tumor Necrosis Factors (Remicade) in Severe Pediatric Crohn Disease

Jean-Pierre Cezard

Corresponding Author

Jean-Pierre Cezard

Pediatric Gastroenterology Unit, Hôpital Robert Debré, Paris, France

Address correspondence and reprint requests to Professor Jean-Pierre Cezard, Service de Gastroenterologie et Nutritions Pédiatriques, Hôpital Robert Debré, 48 Bd Sérurier, 75019 Paris, France (e-mail: [email protected]).Search for more papers by this author
Nizar Nouaili

Nizar Nouaili

Pediatric Gastroenterology Unit, Hôpital Robert Debré, Paris, France

Laboratory of Coprology, Hôpital Pitié Salpétrière, Paris, France

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Cécile Talbotec

Cécile Talbotec

Laboratory of Coprology, Hôpital Pitié Salpétrière, Paris, France

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Jean-Pierre Hugot

Jean-Pierre Hugot

Pediatric Gastroenterology Unit, Hôpital Robert Debré, Paris, France

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Jean-Gérard Gobert

Jean-Gérard Gobert

Pediatric Gastroenterology Unit, Hôpital Necker Enfants Malades, Paris, France

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Jacques Schmitz

Jacques Schmitz

Laboratory of Coprology, Hôpital Pitié Salpétrière, Paris, France

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Jean-François Mougenot

Jean-François Mougenot

Pediatric Gastroenterology Unit, Hôpital Robert Debré, Paris, France

Laboratory of Coprology, Hôpital Pitié Salpétrière, Paris, France

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Corinne Alberti

Corinne Alberti

Pediatric Gastroenterology Unit, Hôpital Robert Debré, Paris, France

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Olivier Goulet

Olivier Goulet

Laboratory of Coprology, Hôpital Pitié Salpétrière, Paris, France

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First published: 01 May 2003
Citations: 39

ABSTRACT

Objectives

To evaluate the efficacy and toxicity of infliximab in children with severe Crohn disease (CD), the authors prospectively monitored 21 children aged 15 ± 2 years with severe CD who they treated with infliximab (5 mg/kg) on days 0, 15, and 45. One patient received only one injection. Eighteen patients were corticosteroid dependent, and 6 were receiving parenteral nutrition. Three patients were corticoid resistant (1 mg/kg/d >15 days). Sixteen had perianal disease.

Results

The Harvey-Bradshaw index (HB) decreased from 8 ± 3 on day 0 to 1 ± 2 on day 45 (P = 0.001). The inflammation factors decreased (P = 0.001), and albumin increased (P = 0.002). Nineteen children were in complete remission (HB < 4) on day 45, and 2 had improved (HB = −6 points). Tumor necrosis factor-α (TNFα) in the stools (n = 16) decreased (P = 0.04). All perianal fistulas (n = 12) were closed by day 90. Fourteen of 21 patients had stopped taking steroids at 3 months, and all had stopped parenteral nutrition. Growth velocity was significantly greater after infliximab administration (Z score, +0.5) than before (−0.45;P = 0.004). Nineteen of 21 patients had relapsed (90%) at 1 year despite continued immunosuppressors. Seven had surgery because of an uncontrolled relapse (5), stenosis (1), or fistula (1). Six patients developed antinuclear antibodies (1/40–1/640e), and two had anti-DNA antibodies. Epstein-Barr virus (EBV) polymerase chain reaction (PCR) values increased (>100-fold) in eight patients. One child developed an anaphylactic reaction to the medication, and one had a catheter-related sepsis.

Conclusion

Infliximab produces spectacular results for children with severe CD and is well tolerated. However, its effect is transitory for many (90%), with frequent relapses despite continued immunosuppressors. Long-term management with infliximab should be tested despite its worrying side effects.

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