Evidence map›Paper›PMID 42039685›Full record

ArticleJTO clinical and research reports2026

Durvalumab Plus Chemotherapy in Patients With

Byoung Chul Cho, Makoto Nishio, Myung-Ju Ahn, Rosario García-Campelo, Santiago Ponce, Christina Baik, Ravi Salgia, Sang-We Kim, Jong Seok Lee, Tatsuya Yoshida and 14 more

Registry-linked trialAbstract read
In one paragraph

Article in JTO clinical and research reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03944772 (A Biomarker-directed Phase 2 Platform Study in Patients With Advanced Non-Small Lung Cancer Whose Disease Has Progressed on First-Line Osimertinib Therapy.), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT03944772 phase2active not recruitingnot on this map

A Biomarker-directed Phase 2 Platform Study in Patients With Advanced Non-Small Lung Cancer Whose Disease Has Progressed on First-Line Osimertinib Therapy.

TypeinterventionalSponsorAstraZenecaRan2019 to 2025Enrolled247ConditionsNon-Small Cell Lung CancerArmsOsimertinib, Savolitinib, Gefitinib, Necitumumab, Durvalumab
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Immune Doublet Checkpoint Inhibition inJTO clinical and research reports · 2026
    Article
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

24 authors.

Byoung Chul ChoDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Makoto NishioDepartment of Thoracic Medical Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Myung-Ju AhnDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Rosario García-CampeloMedical Oncology Unit, University Hospital of A Coruña, A Coruña, Spain.
Santiago PonceDepartment of Medical Oncology, Hospital Universitario 12 de Octubre & Centro Nacional de Investigaciones Oncologicas, Madrid, Spain.
Christina BaikDepartment of Medicine, Division of Medical Oncology, University of Washington School of Medicine, Fred Hutchinson Cancer Center, Seattle, Washington.
Ravi SalgiaDepartment of Medical Oncology and Therapeutics Research, City of Hope National Medical Center, Duarte, California.
Sang-We KimDepartment of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Jong Seok LeeDepartment of Hematology/Oncology, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.
Tatsuya YoshidaDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Helena A YuDepartment of Medicine, Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York.
Sarah B GoldbergDepartment of Medicine (Medical Oncology), Yale School of Medicine, New Haven, Connecticut.
Adrianus Johannes de LangenDepartment of Thoracic Oncology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Xiuning LeThoracic Head and Neck Medical Oncology Department, MD Anderson Cancer Center, Houston, Texas.
Zofia PiotrowskaDepartment of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Jonathan W RiessInternal Medicine - Hematology/Oncology, UC Davis Comprehensive Cancer Center, Sacramento, California.
Kentaro TanakaDepartment of Respiratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Helen AmbroseEarly Oncology, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.
Jan CosaertEarly Global Development, Oncology R&D, AstraZeneca, Den Haag, The Netherlands.
Paula G FraenkelEarly Global Development, Oncology R&D, AstraZeneca, Waltham, Massachusetts.
Kwan Ho TangTranslational Medicine, Research and Early Development, Oncology R&D, AstraZeneca, Waltham, Massachusetts.
Jonathan M LehmanEarly Global Development, Oncology R&D, AstraZeneca, Gaithersburg, Maryland.
Paul SmithOn behalf of Early Oncology, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.
Jonathan W GoldmanDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Gina M Dayton · 2002 to 2026
$84.9M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA093373
6 · The paper itself

Abstract

Introduction: ORCHARD (NCT03944772) was a phase II, biomarker-directed platform study designed to characterize resistance mechanisms and evaluate novel therapy combinations after progressive disease (PD) on first-line osimertinib. We report results of the module assessing durvalumab plus chemotherapy. Methods: Patients with epidermal growth factor receptor ( Results: Overall, 25 patients received more than or equal to 1 dose of durvalumab plus chemotherapy; all had discontinued treatment at the primary analysis data cutoff. Confirmed ORR was 16% (80% confidence interval [CI]: 7-30); response was maintained for more than 6 months in the four patients with confirmed response. Furthermore, 22 patients (88%) had PD and median progression-free survival was 4.8 months (95% CI: 2.6-7.6). Ten patients (40%) had died, and median overall survival was 23.4 months (95% CI: 8.8-not calculable). Nine patients (36%) had grade 3 or higher adverse events, most often neutrophil count decreased (20%). Conclusions: Durvalumab plus chemotherapy demonstrated limited clinical benefit for

Indexed as

ChemotherapyDurvalumabEpidermal growth factor receptor mutatedNon–small cell lung cancerOsimertinib

Identifiers

PMID42039685
PMCPMC13107052

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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.