Evidence map›Paper›PMID 42485106›Full record

Observational studyClinical cancer research : an official journal of the American Association for Cancer Research2026

Utilizing Machine Learning to Identify Multimodal Signatures for Patients Who Would Benefit from the Addition of Tremelimumab to Durvalumab and Chemotherapy (TRIDENT).

Ferdinandos Skoulidis, Salma K Jabbour, Edward B Garon, Puneeth Iyengar, Giorgio Scagliotti, Loïc Ferrer, Guillaume Etchepare, Olivier Gallinato, Jérôme Faure, Paul Bernard and 12 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03164616 (A Phase III, Randomized, Multi-Center, Open-Label, Comparative Global Study to Determine the Efficacy of Durvalumab or Durvalumab and Tremelimumab in Combination With Platinum-Based Chemotherapy for First-Line Treatment in Patients With Metastatic Non Small-Cell Lung Cancer), which is not on this 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.

NCT03164616 phase3active not recruitingnot on this map

A Phase III, Randomized, Multi-Center, Open-Label, Comparative Global Study to Determine the Efficacy of Durvalumab or Durvalumab and Tremelimumab in Combination With Platinum-Based Chemotherapy for First-Line Treatment in Patients With Metastatic Non Small-Cell Lung Cancer (NSCLC) (POSEIDON)

TypeinterventionalSponsorAstraZenecaRan2017 to 2027Enrolled1,186ConditionsNon Small Cell Lung Cancer NSCLCArmsDurvalumab, Tremelimumab, Abraxane + carboplatin, Gemcitabine + cisplatin, Gemcitabine + carboplatin
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

22 authors.

Ferdinandos SkoulidisDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-4676-4503
Salma K JabbourDepartment of Radiation Oncology, Rutgers Cancer Institute, New Brunswick, New Jersey.ORCID 0000-0001-8200-5371
Edward B GaronDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California.ORCID 0000-0001-7077-8801
Puneeth IyengarRadiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-3740-7915
Giorgio ScagliottiUniversity of Turin , Torino, Italy.ORCID 0000-0001-6646-958X
Loïc FerrerSOPHiA GENETICS, Pessac, France.ORCID 0000-0002-2107-0118
Guillaume EtchepareSOPHiA GENETICS, Pessac, France.ORCID 0009-0004-9410-0252
Olivier GallinatoSOPHiA GENETICS, Pessac, France.ORCID 0009-0002-7315-3828
Jérôme FaureSOPHiA GENETICS, Pessac, France.ORCID 0009-0008-2969-2270
Paul BernardSOPHiA GENETICS, Pessac, France.ORCID 0009-0001-4999-7388
Thierry ColinSOPHiA GENETICS, Pessac, France.ORCID 0009-0005-8740-7341
Philippe MenuSOPHiA GENETICS, Rolle, Switzerland.ORCID 0000-0002-1395-6410
Yian LinAstraZeneca, South San Francisco, California.ORCID 0009-0007-7583-0825
Ling CaiAstraZeneca, South San Francisco, California.ORCID 0009-0003-5086-3509
Ammar Ahmed ChaudhryAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0002-2126-0587
Amanda RemorinoAstraZeneca, Barcelona, Spain.ORCID 0009-0009-6150-2016
Ross StewartAstraZeneca, Cambridge, United Kingdom.ORCID 0000-0003-0188-7814
Luisa Luciani-SilvermanAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0003-3330-0210
Katy MillerAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0004-5320-1225
David DellamonicaAstraZeneca, Baar, Switzerland.ORCID 0000-0002-0350-1332
Jolyon FariaAstraZeneca, Cambridge, United Kingdom.ORCID 0009-0003-5728-8578
Yiduo ZhangAstraZeneca, Shanghai, China.ORCID 0000-0002-1978-9713

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePOSEIDON (NCT03164616) was a randomized, open-label, multicenter phase III trial comparing first-line durvalumab with or without tremelimumab in combination with chemotherapy versus chemotherapy alone in patients with metastatic non-small cell lung cancer (NSCLC). Overall survival (OS) and progression-free survival were significantly increased in the tremelimumab plus durvalumab and chemotherapy arm. We conducted a post hoc analysis (TRIDENT) to identify patients who may receive greater OS benefit from the addition of tremelimumab to durvalumab and chemotherapy. EXPERIMENTAL

designThis analysis included clinical, genomic, and radiomic data from the POSEIDON trial (data cutoff March 12, 2021). Machine learning models leveraging multimodal data were trained to identify subpopulations of patients who benefit from the addition of tremelimumab to first-line durvalumab and chemotherapy.

resultsUsing clinical and genomic data, the model was able to predict treatment benefit from adding tremelimumab to first-line durvalumab and chemotherapy, with the top ranked 50% of patients with nonsquamous tumors achieving a hazard ratio of 0.56 (95% confidence interval, 0.33-0.97). EGFR wild type, FGFR3 wild type, CDKN2A wild type, KRAS mutations, and STK11 mutations were the factors most associated with higher OS benefit.

conclusionsBy utilizing machine learning models to analyze POSEIDON data, we yielded genetic signatures identifying patients with nonsquamous metastatic NSCLC who may derive greater OS benefit from the addition of tremelimumab to first-line durvalumab and chemotherapy. Such approaches could be used in the future to enhance precision in tailoring therapies for individual patients.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungLung NeoplasmsMachine LearningBiomarkers, TumorClinical Trials, Phase III as TopicFemaleHumansMaleMiddle AgedMulticenter Studies as TopicRadiomicsRandomized Controlled Trials as TopicAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBiomarkers, Tumordurvalumabtremelimumab

Identifiers

PMID42485106
PMCPMC13628095

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Registered trials

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.