Evidence map›Paper›PMID 40229450›Full record

ArticleNPJ precision oncology2025

Predicting survival in prospective clinical trials using weakly-supervised QSP.

Matthew West, Kenta Yoshida, Jiajie Yu, Vincent Lemaire

Abstract read
In one paragraph

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Matthew WestDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Kenta YoshidaModeling and Simulation, Clinical Pharmacology, Genentech Inc., South San Francisco, CA, USA.
Jiajie YuClinical Pharmacology, Genentech Inc., South San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-6975-5047
Vincent LemaireModeling and Simulation, Clinical Pharmacology, Genentech Inc., South San Francisco, CA, USA. lemaire.vincent@gene.com.ORCID http://orcid.org/0000-0003-2086-6787

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative systems pharmacology (QSP) models of cancer immunity provide mechanistic insights into cellular dynamics and drug effects that are difficult to study clinically. However, their inability to predict patient survival mechanistically limits their utility in anti-cancer drug development. To overcome this, we link virtual patients from a QSP model to real clinical trial patients. Using data from atezolizumab trials in non-small cell lung cancer, we show that tumor-based linkage effectively captures survival outcomes. By treating linked survival and censoring as weak supervision labels, we trained survival models using only QSP model covariates, without clinical covariates. Our approach also predicts survival for treatments not included in training data. Specifically, we accurately estimated survival hazard ratios (HR) for chemotherapy monotherapy and atezolizumab plus chemotherapy combination. The predicted HR of 0.70 (95% prediction interval [PI] 0.55-0.86) closely matches the observed HR of 0.79 (95% PI 0.64-0.98) from the IMpower130 trial.

Identifiers

PMID40229450
PMCPMC11997190

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LicenceCC BY-NC-ND
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Registered trials

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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.