Evidence map›Paper›PMID 41372843›Full record

ArticleBMC cancer2025

Effective serum concentration of high-dose methotrexate therapy for osteosarcoma with dose adjustment for pharmacokinetic parameters: a retrospective study.

Ayumu Nagamine, Takuya Araki, Hideaki Yashima, Akane Kamimura, Takumi Shiraishi, Takashi Yanagawa, Kyoko Obayashi, Koujirou Yamamoto

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ayumu NagamineEducation Center for Clinical Pharmacy, Faculty of Pharmacy, Takasaki University of Health and Welfare, 60 Nakaorui-machi, Takasaki, Gunma, 370- 0033, Japan.
Takuya ArakiDepartment of Clinical Pharmacology and Therapeutics, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371- 8511, Japan. tkyaraki@gunma-u.ac.jp.
Hideaki YashimaDepartment of Clinical Pharmacology and Therapeutics, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371- 8511, Japan.
Akane KamimuraLaboratory of Clinical Pharmacy, Faculty of Pharmacy, Takasaki University of Health and Welfare, 60 Nakaorui-machi, Takasaki, Gunma, 370-0033, Japan.
Takumi ShiraishiLaboratory of Clinical Pharmacy, Faculty of Pharmacy, Takasaki University of Health and Welfare, 60 Nakaorui-machi, Takasaki, Gunma, 370-0033, Japan.
Takashi YanagawaDepartment of Orthopaedic Surgery, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Kyoko ObayashiEducation Center for Clinical Pharmacy, Faculty of Pharmacy, Takasaki University of Health and Welfare, 60 Nakaorui-machi, Takasaki, Gunma, 370- 0033, Japan.
Koujirou YamamotoDepartment of Clinical Pharmacology and Therapeutics, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371- 8511, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn high-dose methotrexate (MTX) (HD-MTX) therapy, a dosage regimen utilizing the pharmacokinetic (PK) parameters of individual patients (PK method) has been developed to successfully reduce the intra- and inter-individual variability of serum MTX concentration. In this study, we evaluated the relationship between the therapeutic effect and serum MTX concentration in HD-MTX therapy performed under conditions in which the serum MTX concentration was precisely controlled using the PK method.

methodsHD-MTX therapy consisted of 1 h of rapid dosing and 5 h of maintenance dosing, with a target serum concentration of 700–1000 µmol/L 1–6 h after the start of administration. The initial MTX dose was determined based on the body surface area, and subsequent courses were determined using PK parameters calculated from changes in MTX concentration at 1, 2, 4, 6, 7, 9, 12, 24, 48, and 72 h after the start of MTX administration. The relationship between the maximum serum MTX concentration (Cmax) and mean concentration from 1 to 6 h after MTX administration [Cmean(1−6)] and efficacy was evaluated. The cut-off values for Cmax and Cmean(1−6) were the values with the best sensitivity and specificity in terms of 5-year survival in the receiver operating characteristic curve.

resultsWe included 33 patients with osteosarcoma without distant metastasis who underwent HD-MTX therapy. Those with a Cmean(1−6) > 768 µmol/L had significantly longer overall survival (OS) (p = 0.010) and tended to have longer event-free survival (EFS) (p = 0.061), with a 5-year survival rate as high as 92.9% (p = 0.077). In contrast, prolonged OS, EFS, and 5-year survival rates were observed in patients with Cmax >936 µmol/L, but none of these differences were significant (p = 0.088, 0.200, and 0.103, respectively). Moreover, OS and EFS improved for Cmean(1−6) > 768 µmol/L regardless of Cmax. In a subgroup analysis of 24 patients aged < 20 years, OS and EFS were significantly prolonged in patients with a Cmean(1−6) > 768 µmol/L (p = 0.010 and 0.025, respectively).

conclusionsThe usefulness of the serum MTX concentration was demonstrated by designing dosing using the PK method. Furthermore, Cmean(1−6) contributed more to prolonging OS and EFS than Cmax.

Indexed as

Antimetabolites, AntineoplasticBone NeoplasmsMethotrexateOsteosarcomaAdolescentAdultChildDose-Response Relationship, DrugFemaleHumansMaleRetrospective StudiesTreatment OutcomeYoung AdultAntimetabolites, AntineoplasticMethotrexateEvent-free survivalHigh-dose methotrexateOsteosarcomaOverall survivalPharmacokineticTarget concentrationTherapeutic drug monitoring

Identifiers

PMID41372843
PMCPMC12822136

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.