Related Experiment Videos

Statistical examination to determine whether only 48-h value for serum concentration during high-dose methotrexate

Yuko Kanbayashi1, Kenichi Nomura, Kousuke Okamoto

  • 1Department of Hospital Pharmacy, Kyoto Prefectural University of Medicine, Kawaramachi Hirokoji, Kamigyo-ku, Japan. ykokanba@koto.kpu-m.ac.jp

Annals of Hematology
|April 29, 2010
PubMed

Insights

High-dose methotrexate (HD-MTX) therapy can cause adverse events. A longer infusion time, higher dose, and combination chemotherapy predict toxicity, not just serum MTX levels at 48 hours.

Area of Science:

  • Oncology
  • Pharmacology
  • Clinical Medicine

Background:

  • Sustained high serum methotrexate (MTX) concentrations (>1.0 microM) for 48 hours predict toxicity.
  • Severe adverse events can occur during high-dose (HD) MTX therapy even with acceptable serum MTX levels.

Purpose of the Study:

  • To identify predictors of adverse events in patients receiving HD-MTX therapy.
  • To determine if the 48-hour serum MTX level is a significant predictor of clinical adverse events.

Main Methods:

  • Retrospective study of 32 hematological patients (58 episodes) treated with HD-MTX.
  • Ordered logistic regression analysis to identify predictors of adverse events.

Main Results:

  • Longer infusion time (24-h C-IV) predicted fatigue (OR=2.890) and neutropenia (OR=2.573).
  • Higher MTX dose (OR=2.282) and combination chemotherapy (OR=2.177) predicted stomatitis.
  • The 48-hour serum MTX value was not a significant predictor of clinical adverse events.

Conclusions:

  • Longer infusion times are significant predictors of fatigue and neutropenia in HD-MTX therapy.
  • Higher doses and combination chemotherapy predict stomatitis.
  • The 48-hour serum MTX level alone is insufficient for predicting toxicity in HD-MTX therapy.

Related Concept Videos

Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations01:15

Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations

Gentamicin, an aminoglycoside antibiotic, is commonly administered via intermittent intravenous infusion to treat severe infections. An intermittent one-hour infusion of gentamicin, administered at eight-hour intervals, allows for precise control of plasma drug concentrations, minimizing toxicity while ensuring therapeutic efficacy. Pharmacokinetic principles govern the dynamics of plasma concentrations and can be mathematically described using specific equations.The plasma drug concentration...
Dosage Regimen: Multiple Oral Dosage01:25

Dosage Regimen: Multiple Oral Dosage

Understanding how a drug's concentration fluctuates within the body over time is crucial in pharmacokinetics, particularly with multiple oral doses. A graphical representation of multiple oral dosages provides insight into these dynamics. Typical accumulation curves of a drug's concentration in the body reveal a sawtooth pattern, indicating periodic peaks and troughs correlating with each dose administration and the drug's subsequent elimination.The plasma concentration at any time during an...
Therapeutic Drug Monitoring: Drug Analysis Methods01:26

Therapeutic Drug Monitoring: Drug Analysis Methods

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood or body tissues to tailor drug therapy effectively. This monitoring is critical for managing drugs with narrow therapeutic indices like digoxin and phenytoin, ensuring they are both safe and effective. For instance, monitoring theophylline levels in asthma patients involves precision and sensitivity to adjust doses according to individual responses to therapy, ensuring efficacy and...
Dosage Regimens: Partial Pharmacokinetic Parameters01:01

Dosage Regimens: Partial Pharmacokinetic Parameters

It is not uncommon for complete drug pharmacokinetic profiles to remain elusive in pharmacokinetics. This necessitates certain educated assumptions by pharmacokineticists to determine appropriate dosage regimens without comprehensive pharmacokinetic data from animal or human studies. One prevalent assumption is setting the bioavailability factor, denoted as F, to 1 or 100%. This assumption caters to the scenario where a drug doesn't achieve full systemic absorption, resulting in the patient...
Dosage Regimen Designs: Nomograms and Tabulations01:23

Dosage Regimen Designs: Nomograms and Tabulations

Nomograms and tabulations are vital tools used by clinicians to design accurate and individualized dosage regimens. These instruments provide a straightforward method for adjusting dosages based on individual patient characteristics, including age, weight, and physiological condition. The foundation of a drug's nomogram is population pharmacokinetic data collected and analyzed using specific models. This data simplifies complex equations, presenting them diagrammatically or tabularly for easy...