Evidence map›Paper›PMID 39558509›Full record

ArticleClinical and translational science2024

Integrating real-world data and machine learning: A framework to assess covariate importance in real-world use of alternative intravenous dosing regimens for atezolizumab.

Bianca Vora, Ashutosh Jindal, Erick Velasquez, James Lu, Benjamin Wu

Abstract read
In one paragraph

Article in Clinical and translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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

5 authors.

Bianca VoraClinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.ORCID 0000-0002-0501-1804
Ashutosh JindalClinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.ORCID 0009-0002-6106-0958
Erick VelasquezClinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.ORCID 0000-0002-0874-4317
James LuClinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.ORCID 0000-0002-9687-5607
Benjamin WuClinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.ORCID 0000-0001-6443-3671

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increase in the availability of real-world data (RWD), in combination with advances in machine learning (ML) methods, provides a unique opportunity for the integration of the two to explore complex clinical pharmacology questions. Here we present a recently developed RWD/ML framework that utilizes ML algorithms to understand the influence and importance of various covariates on the use of a given dose and schedule for drugs that have multiple approved dosing regimens. To demonstrate the application of this framework, we present atezolizumab as a use case on account of its three approved alternative intravenous (IV) dosing regimens. As expected, the real-world use of atezolizumab has generally been increasing since 2016 for the 1200 mg every 3 weeks regimen and since 2019 for the 1680 mg every 4 weeks regimen. Out of the ML algorithms evaluated, XGBoost performed the best, as measured by the area under the precision-recall curve, with an emphasis on the under-sampled class given the imbalance in the data. The importance of features was measured by Shapley Additive exPlanations (SHAP) values and showed metastatic breast cancer and use of protein-bound paclitaxel as the most correlated with the use of 840 mg every 2 weeks. Although patient usage data for alternative IV dosing regimens are still maturing, these analyses provide initial insights on the use of atezolizumab and set up a framework for the re-analysis of atezolizumab (at a future data cut) as well as application to other molecules with approved alternative dosing regimens.

Indexed as

Antibodies, Monoclonal, HumanizedMachine LearningAdministration, IntravenousAgedAlgorithmsDose-Response Relationship, DrugDrug Administration ScheduleFemaleHumansInfusions, IntravenousMaleMiddle AgedAntibodies, Monoclonal, Humanizedatezolizumab

Identifiers

PMID39558509
PMCPMC11573720

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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.