Evidence map›Paper›PMID 42297911›Full record

ArticleNPJ precision oncology2026

Optimization of first-line treatment selection in advanced pancreatic adenocarcinoma using artificial intelligence.

Sebastian Cole, Paul Campitelli, Brian Grieb, Igor Astsaturov, Daniel Von Hoff, Harshabad Singh, Michael J Pishvaian, Tanios S Bekaii-Saab, Peter J Hosein, Philip A Philip and 6 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 2026. 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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0citing papers in PubMed
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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

16 authors.

Sebastian ColeCaris Life Sciences, Irving, TX, USA.
Paul CampitelliCaris Life Sciences, Irving, TX, USA.
Brian GriebTennessee Oncology, Nashville, TN, USA.
Igor AstsaturovFox Chase Cancer Center, Philadelphia, PA, USA.
Daniel Von HoffTranslational Genomics Research Institute, Phoenix, AZ, USA.
Harshabad SinghMass General Brigham Cancer Institute, Boston, MA, USA.
Michael J PishvaianJohns Hopkins University, Washington, DC, USA.
Tanios S Bekaii-SaabMayo Clinic, Phoenix, AZ, USA.
Peter J HoseinUniversity of Miami, Miami, FL, USA.
Philip A PhilipHenry Ford Cancer Institute, Wayne State University, Detroit, MI, USA.
Anthony HelmstetterCaris Life Sciences, Irving, TX, USA.
Todd ManeyCaris Life Sciences, Irving, TX, USA.
Jennifer R RibeiroCaris Life Sciences, Irving, TX, USA.
James HamrickCaris Life Sciences, Irving, TX, USA. jhamrick@carisls.com.
Daniel MageeCaris Life Sciences, Irving, TX, USA.
David SpetzlerCaris Life Sciences, Irving, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Improved clinical outcomes are reported for patients with advanced pancreatic adenocarcinoma (PDAC) treated with first-line FOLFIRINOX/NALIRIFOX, but elderly patients with comorbidities are more often treated with gemcitabine/nab-paclitaxel (gem/nab-p). There is currently no comprehensive method to optimize first-line treatment selection between these regimens. We developed a propensity score matched, transcriptomic-based AI model using 2202 molecularly-profiled PDAC specimens to provide clinically relevant treatment recommendations and prognostic information. In a testing dataset of patients predicted to have superior outcomes on first-line FOLFIRINOX, time-to-next-treatment (TTNT) and overall survival (OS) were significantly longer for patients treated with FOLFIRINOX first (HRs = 0.55 and 0.48, respectively, p < 0.001). Patients recommended for gem/nab-p treatment had similar outcomes on either treatment, but a subset had improved outcomes on gem/nab-p. Approximately half of patients had received the opposite therapy from the model recommendation. Applied clinically, this model could improve treatment decision-making in advanced PDAC in the first-line setting.

Identifiers

PMID42297911
PMCPMC13507153

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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.