A newly published retrospective study found that patients who received a combination therapy with infliximab and azathioprine early on had significantly increased linear growth compared to patients whose therapy was stepped up.
Conventionally, treatment for pediatric Crohn disease (CD) has focused on inducing remission with corticosteroids and maintaining remission with immunomodulators. Those patients who are refractory or intolerant to such a treatment approach are sometimes considered candidates for treatment with infliximab (an approach known as “step-up” therapy), but data on the use of early infliximab treatment in pediatric patients with CD have thus far been limited.
Information about growth failure in pediatric patients with CD has also been limited, though growth failure is recognized as a characteristic of the disease; proposed factors contributing to the problem are chronic undernutrition and the presence of inflammatory cytokines secreted from the intestine. Use of corticosteroids also increases the risk of growth failure.
A newly published retrospective study, appearing in Gut and Liver, sought to evaluate the impact of different treatment approaches on linear growth of pediatric patients with CD, and found that patients who received a combination therapy with infliximab and azathioprine early on had significantly increased linear growth compared to patients whose therapy was stepped up.
A total of 33 patients were included in the study; 16 had been allocated to the step-up group and 17 to the early combined immunosuppression group. Patients in the step-up group received an oral corticosteroid dose of 1 mg/kg daily for induction therapy, which was tapered over 8 weeks, and oral azathioprine and mesalazine for maintenance therapy (infliximab could be added in this group if necessary to maintain clinical remission). The early combined immunosuppression group received infliximab at infused doses of 5 mg/kg at weeks 0, 2, and 6 for induction, and every 8 weeks thereafter. Patients in this group initiated azathioprine at daily doses of 0.5 to 1 mg/kg, and doses were adjusted as required.
Z-scores for height (which measure children’s stature for age) for the 2 groups were as follows at 1, 2, and 3 years after diagnosis:
“Our study showed that an early combined immunosuppression strategy was superior to step-up strategy in improving long-term height z-scores,” write the authors, who add that “long-term restoration of linear growth was superior in the early combined immunosuppression when compared from diagnosis.” The authors conclude that early introduction of biologics at the time of diagnosis with pediatric CD should be considered in terms of improving linear growth.
The Top 5 Most-Read Gastroenterology Articles of 2024
December 21st 2024The top gastroenterology biosimilar news from 2024 highlight fluctuations in the adalimumab biosimilar market throughout the year, while FDA and European approvals for ustekinumab biosimilars are set to improve access and reduce costs for patients with Crohn disease and ulcerative colitis.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
13 Strategies to Avoid the Nocebo Effect During Biosimilar Switching
December 18th 2024A systematic review identified 13 strategies, including patient and provider education, empathetic communication, and shared decision-making, to mitigate the nocebo effect in biosimilar switching, emphasizing the need for a multifaceted approach to improve patient perceptions and therapeutic outcomes.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Stable Patient Satisfaction Found After Switching From the Humira or Biosimilar CT-P17
December 14th 2024A real-world study in France found patient satisfaction was stable after switching from either the reference product or a low-concentration adalimumab biosimilar to the adalimumab biosimilar CT-P17, a high-concentration, citrate-free formulation.
Eye on Pharma: Golimumab Biosimilar Update; Korea Approves Denosumab; Xbrane, Intas Collaboration
December 10th 2024Alvotech and Advanz Pharma have submitted a European marketing application for their golimumab biosimilar to treat inflammatory diseases, while Celltrion secured Korean approval for denosumab biosimilars, and Intas Pharmaceuticals partnered with Xbrane Biopharma on a nivolumab biosimilar.