Evidence map›Paper›PMID 36624662›Full record

ArticleJournal of clinical pharmacology2023

In Silico Re-Optimization of Atezolizumab Dosing Using Population Pharmacokinetic Simulation and Exposure-Response Simulation.

Cody J Peer, Keith T Schmidt, Oluwatobi Arisa, William J Richardson, Koosha Paydary, Daniel A Goldstein, James L Gulley, William D Figg, Mark J Ratain

Abstract read
In one paragraph

Article in Journal of clinical pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Pharmacokinetic insights into atezolizumab SC: viability of extended dosing intervals beyond the standard regimen.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Observational
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Cody J PeerClinical Pharmacology Program, National Cancer Institute, Bethesda, Maryland, USA.ORCID 0000-0001-9395-3473
Keith T SchmidtClinical Pharmacology Program, National Cancer Institute, Bethesda, Maryland, USA.
Oluwatobi ArisaClinical Pharmacology Program, National Cancer Institute, Bethesda, Maryland, USA.
William J RichardsonClinical Pharmacology Program, National Cancer Institute, Bethesda, Maryland, USA.
Koosha PaydaryDepartment of Medicine, Section of Hematology/Oncology, and Committee on Clinical Pharmacology & Pharmacogenomics, The University of Chicago, Chicago, Illinois, USA.
Daniel A GoldsteinFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
James L GulleyGenitourinary Malignancies Branch, National Cancer Institute, Bethesda, Maryland, USA.
William D FiggClinical Pharmacology Program, National Cancer Institute, Bethesda, Maryland, USA.
Mark J RatainDepartment of Medicine, Section of Hematology/Oncology, and Committee on Clinical Pharmacology & Pharmacogenomics, The University of Chicago, Chicago, Illinois, USA.

Funding

Using Clinical Pharmacology Principles to Develop New Anticancer TherapiesZICSC006537 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI FIGG, WILLIAM DOUGLAS · 2009 to 2025
$14.4M
CLINICAL THERAPEUTICST32GM007019 · NIGMS · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell, MARK J RATAIN · 1985 to 2026
$8.7M
Using Clinical Pharmacology Principles to Develop New Anticancer TherapiesZ01SC006537 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI FIGG, WILLIAM DOUGLAS · 1997 to 2008
$379k
Intramural NIH HHS Z01 SC006537Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIC SC006537NIGMS NIH HHS T32 GM007019
6 · The paper itself

Abstract

Atezolizumab, a humanized monoclonal antibody against programmed cell death ligand 1 (PD-L1), was initially approved in 2016, around the same time that the sponsor published the minimum serum concentration to maintain the saturation of receptor occupancy (6 μg/mL). The initially approved dose regimen of 1200 mg every 3 weeks (q3w) was subsequently modified to 840 mg q2w or 1680 mg q4w through pharmacokinetic simulations. Yet, each standard regimen yields steady-state trough concentrations (C

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntibodies, Monoclonal, HumanizedComputer SimulationHumansTreatment OutcomeAntibodies, Monoclonal, Humanizedatezolizumabclinical trialsimmunopharmacologymodeling & simulationoncologypopulation pharmacokinetics

Identifiers

PMID36624662
PMCPMC10175103

What OpenQuestion holds

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Registered trials

None linked

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.