Evidence map›Paper›PMID 38898120›Full record

Trial reportNature medicine2024

Entrectinib in ROS1-positive advanced non-small cell lung cancer: the phase 2/3 BFAST trial.

Solange Peters, Shirish M Gadgeel, Tony Mok, Ernest Nadal, Saadettin Kilickap, Aurélie Swalduz, Jacques Cadranel, Shunichi Sugawara, Chao-Hua Chiu, Chong-Jen Yu and 11 more

Registry-linked trialAbstract readClinical Trial, Phase IIClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Nature medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03178552 (A Phase II/III Multicenter Study Evaluating the Efficacy and Safety of Multiple Targeted Therapies as Treatments for Patients With Advanced or Metastatic Non-Small Cell Lung Cancer), which is not on this map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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.

NCT03178552 phase2 / phase3active not recruitingnot on this map

A Phase II/III Multicenter Study Evaluating the Efficacy and Safety of Multiple Targeted Therapies as Treatments for Patients With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) Harboring Actionable Somatic Mutations Detected in Blood (B-FAST: Blood-First Assay Screening Trial)

TypeinterventionalSponsorHoffmann-La RocheRan2017 to 2026Enrolled1,000ConditionsNon-Small Cell Lung CancerArmsAlectinib, Atezolizumab, Pemetrexed, Cisplatin, Carboplatin
3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

  1. Review
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  8. Review
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  11. Neuro-Cancer Interactions Shape Glioma Intratumoral Heterogeneity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  12. Article
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  14. Review
  15. Article
  16. Translational cancer research · 2025
    Article
  17. 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

21 authors.

Solange PetersLausanne University Hospital, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland. solange.peters@chuv.ch.ORCID 0000-0002-0412-7143
Shirish M GadgeelHenry Ford Cancer Institute/Henry Ford Health System, Detroit, MI, USA.
Tony MokState Laboratory of Translational Oncology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, Hong Kong SAR.ORCID 0000-0002-8251-0551
Ernest NadalThoracic Oncology Unit, Department of Medical Oncology, Catalan Institute of Oncology (ICO), L'Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0002-9674-5554
Saadettin KilickapDepartment of Medical Oncology, Instinye University Faculty of Medicine, Istanbul, Turkey.
Aurélie SwalduzDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Jacques CadranelDepartment of Pneumology and Thoracic Oncology, APHP, Hôpital Tenon and GRC04 Theranoscan Sorbonne Université, Paris, France.
Shunichi SugawaraDepartment of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan.ORCID 0000-0002-3427-4558
Chao-Hua ChiuDepartment of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Chong-Jen YuDepartment of Internal Medicine, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu, Taiwan.ORCID 0000-0001-5664-9392
Mor MoskovitzThoracic Cancer Service, Davidoff Cancer Center, Rabin Medical Center, Beilinson Campus, Petah Tikva, Israel.
Tomohiro TanakaChugai Pharmaceutical Co. Ltd, Tokyo, Japan.
Rhea NersesianGenentech Inc., South San Francisco, CA, USA.
Sarah M ShaganGenentech Inc., South San Francisco, CA, USA.ORCID 0000-0003-0071-3791
Margaret MaclennanSyneos Health, Edinburgh, UK.
Michael MathisenGenentech Inc., South San Francisco, CA, USA.
Vijay Bhagawati-PrasadF. Hoffmann-La Roche Ltd, Welwyn Garden City, UK.
Cheick DiarraGenentech Inc., South San Francisco, CA, USA.
Zoe June AssafGenentech Inc., South San Francisco, CA, USA.ORCID 0000-0002-3469-6697
Venice ArcherF. Hoffmann-La Roche Ltd, Welwyn Garden City, UK.
Rafal DziadziuszkoDepartment of Oncology and Radiotherapy and Early Clinical Trials Unit, Medical University of Gdansk, Gdansk, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although comprehensive biomarker testing is recommended for all patients with advanced/metastatic non-small cell lung cancer (NSCLC) before initiation of first-line treatment, tissue availability can limit testing. Genomic testing in liquid biopsies can be utilized to overcome the inherent limitations of tissue sampling and identify the most appropriate biomarker-informed treatment option for patients. The Blood First Assay Screening Trial is a global, open-label, multicohort trial that evaluates the efficacy and safety of multiple therapies in patients with advanced/metastatic NSCLC and targetable alterations identified by liquid biopsy. We present data from Cohort D (ROS1-positive). Patients ≥18 years of age with stage IIIB/IV, ROS1-positive NSCLC detected by liquid biopsies received entrectinib 600 mg daily. At data cutoff (November 2021), 55 patients were enrolled and 54 had measurable disease. Cohort D met its primary endpoint: the confirmed objective response rate (ORR) by investigator was 81.5%, which was consistent with the ORR from the integrated analysis of entrectinib (investigator-assessed ORR, 73.4%; data cutoff May 2019, ≥12 months of follow-up). The safety profile of entrectinib was consistent with previous reports. These results demonstrate consistency with those from the integrated analysis of entrectinib in patients with ROS1-positive NSCLC identified by tissue-based testing, and support the clinical value of liquid biopsies to inform clinical decision-making. The integration of liquid biopsies into clinical practice provides patients with a less invasive diagnostic method than tissue-based testing and has faster turnaround times that may expedite the reaching of clinical decisions in the advanced/metastatic NSCLC setting. ClinicalTrials.gov registration: NCT03178552 .

Indexed as

BenzamidesCarcinoma, Non-Small-Cell LungIndazolesLung NeoplasmsProtein-Tyrosine KinasesProto-Oncogene ProteinsAdultAgedAged, 80 and overBiomarkers, TumorFemaleHumansLiquid BiopsyMaleMiddle AgedProtein Kinase InhibitorsBenzamidesBiomarkers, TumorentrectinibIndazolesProtein Kinase InhibitorsProtein-Tyrosine KinasesProto-Oncogene ProteinsROS1 protein, human

Identifiers

PMID38898120
PMCPMC11271410

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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.