Homocysteine and methylmalonic acid: markers to predict and avoid toxicity from pemetrexed therapy

The purpose of this study was to identify predictive factors for severe toxicity caused by antifolate-chemotherapy using pemetrexed (ALIMTA, LY231514), as a model. Data on potential predictive factors for severe toxicity from pemetrexed were collected from 246 patients treated between 1995 and 1999....

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Veröffentlicht in:Molecular cancer therapeutics 2002-05, Vol.1 (7), p.545
Hauptverfasser: Niyikiza, Clet, Baker, Sharyn D, Seitz, David E, Walling, Jackie M, Nelson, Katrina, Rusthoven, James J, Stabler, Sally P, Paoletti, Paolo, Calvert, A Hilary, Allen, Robert H
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container_end_page
container_issue 7
container_start_page 545
container_title Molecular cancer therapeutics
container_volume 1
creator Niyikiza, Clet
Baker, Sharyn D
Seitz, David E
Walling, Jackie M
Nelson, Katrina
Rusthoven, James J
Stabler, Sally P
Paoletti, Paolo
Calvert, A Hilary
Allen, Robert H
description The purpose of this study was to identify predictive factors for severe toxicity caused by antifolate-chemotherapy using pemetrexed (ALIMTA, LY231514), as a model. Data on potential predictive factors for severe toxicity from pemetrexed were collected from 246 patients treated between 1995 and 1999. Multivariate stepwise regression methods were used to identify markers predictive of severe toxicity. Using a multiple logistic regression model allowed us to quantify the relative risk of developing toxicities and to generate a validated clinical hypothesis on ways to improve the safety profile of pemetrexed. Pretreatment total plasma homocysteine (tHcy) levels significantly predict severe thrombocytopenia and neutropenia with or without associated grade 3/4 diarrhea, mucositis, or infection. Pretreatment methylmalonic acid (MMA) levels significantly and independently predict grade 3/4 diarrhea and mucositis; however, these toxicities are still predicted by tHcy alone. Patients with elevated baseline levels of tHcy alone, or of both tHcy and MMA, were found to have a high risk of severe toxicity that led us to postulate that reducing tHcy would result in a reduction of severe toxicity with no harm to efficacy. This study points out for the first time the importance of pretreatment tHcy levels in predicting severe toxicity associated with an antifolate and sets the stage for a prospective clinical intervention to protect patients from pemetrexed-induced severe toxicity and possibly improve the drug's efficacy. Antifolates as a class have been associated with sporadic severe myelosuppression with gastrointestinal toxicity. Although infrequent, a combination of such toxicities can carry a high risk of mortality. This phenomenon had been unpredictable until now. Our work shows that by measuring tHcy, one can identify patients that are at risk of toxicity before treatment. Most importantly, decreasing homocysteine levels via vitamin supplementation leads to a better safety profile of pemetrexed and possibly to an improved efficacy.
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source MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals
subjects Adult
Aged
Aged, 80 and over
Antineoplastic Agents - adverse effects
Antineoplastic Agents - therapeutic use
Antineoplastic Agents - toxicity
Female
Folic Acid - therapeutic use
Glutamates - adverse effects
Glutamates - therapeutic use
Glutamates - toxicity
Guanine - adverse effects
Guanine - analogs & derivatives
Guanine - therapeutic use
Guanine - toxicity
Homocysteine - pharmacology
Humans
Male
Methylmalonic Acid - pharmacology
Middle Aged
Models, Biological
Multivariate Analysis
Odds Ratio
Pemetrexed
Time Factors
Vitamin B 12 - therapeutic use
title Homocysteine and methylmalonic acid: markers to predict and avoid toxicity from pemetrexed therapy
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