Evidence map›Paper›PMID 37458784›Full record

ArticleCancer chemotherapy and pharmacology2023

Effect of massive ascites on ramucirumab pharmacokinetics in patients with gastrointestinal cancers: a population pharmacokinetic analysis.

Takuya Kaneko, Kosuke Doki, Takeshi Yamada, Yoshiyuki Yamamoto, Toshikazu Moriwaki, Yoshiharu Suzuki, Masato Homma

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Article in Cancer chemotherapy and pharmacology, 2023. 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Takuya KanekoDepartment of Pharmacy, University of Tsukuba Hospital, Ibaraki, Japan.
Kosuke DokiDepartment of Pharmacy, University of Tsukuba Hospital, Ibaraki, Japan. k-doki@md.tsukuba.ac.jp.ORCID 0000-0003-2497-0063
Takeshi YamadaDivision of Gastroenterology, University of Tsukuba Hospital, Ibaraki, Japan.
Yoshiyuki YamamotoDivision of Gastroenterology, University of Tsukuba Hospital, Ibaraki, Japan.
Toshikazu MoriwakiDivision of Gastroenterology, University of Tsukuba Hospital, Ibaraki, Japan.
Yoshiharu SuzukiDepartment of Pharmacy, University of Tsukuba Hospital, Ibaraki, Japan.
Masato HommaDepartment of Pharmacy, University of Tsukuba Hospital, Ibaraki, Japan.
University of Tsukuba · JPUniversity of Tsukuba Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeConsiderable amounts of injected immunoglobulin G-based therapeutic monoclonal antibodies, such as ramucirumab, are distributed into ascites. This study aimed to examine the effect of massive ascites on ramucirumab pharmacokinetics in patients with gastrointestinal cancers.

methodsPopulation pharmacokinetic analysis of ramucirumab was performed using data on serum ramucirumab concentrations of 52 patients with gastrointestinal cancers, including 8 patients with massive ascites. The Bayesian method using the final population pharmacokinetic model was utilized to estimate trough ramucirumab concentrations after the first dose and at steady state.

resultsPopulation pharmacokinetic analysis revealed that massive ascites as well as body weight were influencing factors for ramucirumab clearance. The estimated ramucirumab clearance was significantly higher in patients with massive ascites than in those with no/mild ascites (0.020 ± 0.004 versus 0.013 ± 0.004 L/h, P < 0.001). The estimated trough ramucirumab concentrations were significantly lower in patients with massive ascites than in those with no/mild ascites after the first dose (26.4 ± 6.8 versus 36.1 ± 7.1 μg/mL, P < 0.001) and at steady state (41.4 ± 16.3 versus 65.9 ± 18.0 μg/mL, P < 0.001).

conclusionIn the present study, the presence of massive ascites affected the pharmacokinetics of ramucirumab in patients with gastrointestinal cancers. Our results suggest that dose optimization of ramucirumab may be necessary in patients with massive ascites due to higher ramucirumab clearance.

Indexed as

AscitesGastrointestinal NeoplasmsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBayes TheoremHumansRamucirumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedRamucirumabAscitesClearancePopulation pharmacokinetic analysisRamucirumabSystemic exposure

Identifiers

PMID37458784
OpenAlexW4384525780

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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 Socratic graph.