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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
Abstract:
Sustained elevation of serum methotrexate (MTX) concentrations (>1.0 microM) for 48 h (48-h value) has been found to have predictive significance for the development of toxicity. However, we sometimes experience severe adverse events during high-dose (HD) MTX therapy even if serum MTX concentrations comply with recommended values. We performed a retrospective study to identify predictors for occurrence of adverse events and examined whether only the 48-h value is a statistically significant predictor for clinical adverse events during HD MTX therapy. The subjects were 32 hematological patients (n = 58 episodes) treated with MTX at Kyoto Prefectural University of Medicine between February 2003 and July 2007. Ordered logistic regression analysis was used to identify predictors for occurrence of adverse events. The predictive factors identified were: 24-h continuous infusion therapy (24-h C-IV) (long infusion time) [odds ratio (OR) = 2.890, confidence interval (CI) =1.493-5.594; P = 0.0016] for fatigue, higher dose [OR = 2.282, CI = 1.287-4.046; P = 0.0048] and combination chemotherapy [OR = 2.177, CI = 1.059-4.477; P = 0.0344] for stomatitis, and 24-h C-IV [OR = 2.573, CI = 1.101-6.016; P = 0.0291] for neutropenia. We found that only the 48-h value was not a predictor for clinical adverse events for HD MTX therapy. A major limitation of the present study was the small number of participants. However, our findings suggest that there is evidence that a long infusion time is a significant predictor for general fatigue and neutropenia, while a higher dose and combination chemotherapy are predictors for stomatitis.
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.
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