EULAR Suggested New Points on Drug Monitoring in Rheumatic Disease

Therapeutic drug monitoring (TDM) plays a vital role in improving clinical outcomes. There are many knowledge gaps around the potential use of TDM, and many rheumatologists are unaware of the pharmacokinetic properties of the biopharmaceuticals that they prescribe. Although biopharmaceuticals typically have a dose recommendation on their label, research has shown that individual patients have variations in the levels of the drug found in their blood. This finding suggests a potential benefit for dose optimization.

However, the new points highlight that — despite an association with the clinical response — the use of blood concentrations to guide dosing is not recommended due to the lack of an identified optimal range for most biopharmaceuticals in most indications.

New EULAR Operating Procedures

The new European Alliance of Associations for Rheumatology (EULAR) points’ work was completed in line with EULAR standardized operating procedures. All information included in the final paper was based on a systematic literature review and expert consensus.

Overall, 6 overarching principles and 13 points were formulated. The principles define two broad categories of TDM: proactive (scheduled testing irrespective of clinical situation) and reactive (testing in response to particular scenarios).

The principles also reinforce key underlying pharmacokinetic and pharmacodynamic principles, which are relevant to all biopharmaceutical classes. An important consideration is that TDM should be part of a shared decision-making process between the patient and health care professionals, incorporating the patient’s individual experiences and preferences.

The points-to-consider highlight the clinical utility of the measurement and interpretation of biopharmaceutical blood concentrations — as well as anti-drug antibodies in specific clinical scenarios.

They stress that measurements should be performed in a validated laboratory, preferably using a consistent assay over time when measuring anti-drug antibodies.

Advertisement

This new publication highlights the potential clinical utility of the measurement and interpretation of biopharmaceutical blood concentrations and anti-drug antibodies, but places this alongside factors that influence these parameters such as dose, administration interval, body weight, and methotrexate cotreatment, disease activity, and adherence to treatment.

As the field rapidly progresses, it is anticipated that more data will become available, which may prompt an update of these points to consider in the years ahead.

Advertisement

Future research should focus on providing evidence on the effectiveness and safety of TDM, as well as a robust economic evaluation of its utility in patients with various RMDs.



Source-Medindia