Calprotectin and the Magnitude of Antibodies to Infliximab in Clinically-stable Ulcerative Colitis Patients are More Relevant Than Infliximab Trough Levels and Pharmacokinetics for Therapeutic Escalation
Fernando Magro,
Joana Afonso,
Susana Lopes,
Rosa Coelho,
Raquel Gonçalves,
Paulo Caldeira,
Paula Lago,
Helena Tavares de Sousa,
Jaime Ramos,
Ana Rita Gonçalves,
Paula Ministro,
Isadora Rosa,
Ana Isabel Vieira,
Patrícia Andrade,
João-Bruno Soares,
Diana Carvalho,
Paula Sousa,
Tânia Meira,
Joanne Lopes,
Joana Moleiro,
Cláudia Camila Dias,
Amílcar Falcão,
Karel Geboes,
Fatima Carneiro
Affiliations
Fernando Magro
Department of Biomedicine, Unity of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal
Joana Afonso
MedInUP, Centre for Drug Discovery and Innovative Medicines, University of Porto, 4200 Porto, Portugal
Susana Lopes
Gastroenterology Department, Centro Hospitalar São João, Porto, Portugal
Rosa Coelho
Gastroenterology Department, Centro Hospitalar São João, Porto, Portugal
Raquel Gonçalves
Gastroenterology Department, Hospital de Braga, Braga, Portugal
Paulo Caldeira
Gastroenterology Department, Centro Hospitalar do Algarve, Faro, Portugal
Paula Lago
Gastroenterology Department, Centro Hospitalar do Porto, Porto, Portugal
Helena Tavares de Sousa
Gastroenterology Department, Centro Hospitalar do Algarve, Portimão, Portugal
Jaime Ramos
Gastroenterology Department, Centro Hospitalar de Lisboa, Lisboa, Portugal
Ana Rita Gonçalves
Gastroenterology Department, Centro Hospitalar Lisboa Norte, Lisboa, Portugal
Paula Ministro
Gastroenterology Department, Hospital de S. Teotónio, Viseu, Portugal
Isadora Rosa
Gastroenterology Department, Instituto Português de Oncologia de Lisboa, Lisboa, Portugal
Ana Isabel Vieira
Gastroenterology Department, Hospital Garcia de Orta, Almada, Portugal
Patrícia Andrade
Gastroenterology Department, Centro Hospitalar São João, Porto, Portugal
João-Bruno Soares
Gastroenterology Department, Hospital de Braga, Braga, Portugal
Diana Carvalho
Gastroenterology Department, Centro Hospitalar de Lisboa, Lisboa, Portugal
Paula Sousa
Gastroenterology Department, Hospital de S. Teotónio, Viseu, Portugal
Tânia Meira
Gastroenterology Department, Hospital Garcia de Orta, Almada, Portugal
Joanne Lopes
Department of Pathology, Centro Hospitalar São João, Porto, Portugal
Joana Moleiro
Gastroenterology Department, Instituto Português de Oncologia de Lisboa, Lisboa, Portugal
Cláudia Camila Dias
Department of Community Medicine, Information and Health Decision Sciences, Faculty of Medicine, University of Porto, Porto, Portugal
Amílcar Falcão
Faculty of Pharmacy, University of Coimbra, Coimbra, Portugal
Karel Geboes
Department of Pathology, University Hospital of KU Leuven and UZ Gent, Leuven, Belgium
Fatima Carneiro
Department of Pathology, Centro Hospitalar São João, Porto, Portugal
Although infliximab (IFX) is an efficient therapy for ulcerative colitis (UC) patients, a considerably high rate of therapeutic failures still occurs. This study aimed at a better understanding of IFX pharmacokinetics and pharmacodynamics among clinically-asymptomatic UC patients. This was a multicentric and prospective study involving 65 UC patients in the maintenance phase of IFX therapy. There were no significant differences between patients with positive and negative clinical, endoscopic and histological outcomes concerning their IFX trough levels (TLs), area under the IFX concentration vs. time curve (AUC), clearance and antibodies to infliximab (ATI) levels. However, the need to undergo therapeutic escalation later in disease development was significantly associated with higher ATI levels (2.62 μg/mL vs. 1.15 μg/mL, p = 0.028). Moreover, and after adjusting for disease severity, the HR (hazard ratio) for therapeutic escalation was significantly decreased for patients with an ATI concentration below 3 μg/mL (HR = 0.119, p = 0.010), and increased for patients with fecal calprotectin (FC) level above 250 μg/g (HR = 9.309, p = 0.018). In clinically-stable UC patients, IFX pharmacokinetic features cannot predict therapeutic response on a short-term basis. However, high levels of ATIs or FC may be indicative of a future therapeutic escalation.