Evidence map›Paper›PMID 37707791›Full record

Trial reportCancer discovery2023

Neoadjuvant Durvalumab Alone or Combined with Novel Immuno-Oncology Agents in Resectable Lung Cancer: The Phase II NeoCOAST Platform Trial.

Tina Cascone, Gozde Kar, Jonathan D Spicer, Rosario García-Campelo, Walter Weder, Davey B Daniel, David R Spigel, Maen Hussein, Julien Mazieres, Julio Oliveira and 18 more

Open access · hybridAbstract readClinical Trial, Phase IIRandomized Controlled TrialAdaptive Clinical Trial
In one paragraph

Trial report in Cancer discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 5 pooled it
24.6field-weighted citation impact, top 1% of its field
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

101 citing papers in PubMed, 5 syntheses or guidelines pooled it, 107 citations in OpenAlex.

  1. Cancer-related fatigue during treatment with neoadjuvant and/or adjuvant immune checkpoint inhibitors: a systematic review and meta-analysis.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Pooled it
  2. Adjuvant immune checkpoint inhibitors in early-stage non-small cell lung cancer: insights from a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Trial
  8. Trial
  9. Review
  10. Management of borderline resectable NSCLC: a narrative review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  11. RNA therapeutics: current status and future directions.Signal transduction and targeted therapy · 2026
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. A systematic review and meta-analysis on survival, pathological response, and safety of durvalumab in early-stage non-small cell lung cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  17. Review
  18. Review
  19. Article
  20. Article

41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 14 institutions in 7 countries.

Tina CasconeDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0003-3008-5407
Gozde KarAstraZeneca, Translational Medicine, Research and Early Development, Oncology Research and Development, Cambridge, United Kingdom.ORCID 0009-0002-7473-2725
Jonathan D SpicerDepartment of Thoracic Surgery, McGill University, Montreal, Quebec, Canada.ORCID 0000-0003-2708-1309
Rosario García-CampeloMedical Oncology Unit, University Hospital A Coruña, A Coruña, Spain.ORCID 0000-0003-2113-1504
Walter WederThoracic Surgery, Clinic Bethanien, Zurich, Switzerland.ORCID 0009-0008-3641-7568
Davey B DanielSarah Cannon Research Institute/Tennessee Oncology, Nashville, Tennessee.ORCID 0000-0001-9647-0119
David R SpigelSarah Cannon Research Institute/Tennessee Oncology, Nashville, Tennessee.ORCID 0000-0003-3215-9465
Maen HusseinSarah Cannon Research Institute, Florida Cancer Specialists, Leesburg, Florida.ORCID 0000-0001-6160-6776
Julien MazieresThoracic Oncology Department, Toulouse University Hospital, Toulouse, France.ORCID 0000-0002-5921-7613
Julio OliveiraMedical Oncology Department, Portuguese Oncology Institute (IPO-PORTO), Porto, Portugal.ORCID 0000-0002-9576-3486
Edwin H YauDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-3972-0756
Alexander I SpiraVirginia Cancer Specialists, US Oncology Research, NEXT Oncology Virginia, Fairfax, Virginia.ORCID 0000-0003-1303-0447
Valsamo AnagnostouBloomberg-Kimmel Institute for Cancer Immunotherapy, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland.ORCID 0000-0001-9480-3047
Raymond MagerAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0004-6753-7416
Oday HamidAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0001-8846-4795
Lin-Yang ChengAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0003-1781-3270
Ying ZhengAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0008-4072-1773
Jorge BlandoAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0003-3628-6656
Tze Heng TanAstraZeneca, Munich, Germany.ORCID 0009-0004-6730-6183
Michael SuraceAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0000-8326-5159
Jaime Rodriguez-CanalesAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0002-0885-2377
Vancheswaran GopalakrishnanAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0002-8704-035X
Bret R SellmanAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0008-4254-8134
Italia GrengaAstraZeneca, Waltham, Massachusetts.ORCID 0009-0006-0585-0532
Yee Soo-HooAstraZeneca, Gaithersburg, Maryland.ORCID 0009-0001-5997-8682
Rakesh KumarAstraZeneca, Gaithersburg, Maryland.ORCID 0000-0002-4627-3667
Lara McGrathAstraZeneca, Waltham, Massachusetts.ORCID 0000-0001-6190-4802
Patrick M FordeBloomberg-Kimmel Institute for Cancer Immunotherapy, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland.ORCID 0000-0001-6925-6344
AstraZeneca (Japan) · JPMassachusetts Medical Society · USSidney Kimmel Comprehensive Cancer Center · USTennessee Oncology · USFlorida Cancer Specialists & Research Institute · USInstituto Português de Oncologia Francisco Gentil · PTKrankenhaus Bethanien · DEMcGill University · CARoswell Park Comprehensive Cancer Center · USThe University of Texas MD Anderson Cancer Center · USTranslational Research in Oncology · FRUniversidade da Coruña · ESUniversité Fédérale de Toulouse Midi-Pyrénées · FRVirginia Cancer Specialists · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neoadjuvant chemoimmunotherapy improves pathologic complete response rate and event-free survival in patients with resectable non-small cell lung cancer (NSCLC) versus chemotherapy alone. NeoCOAST was the first randomized, multidrug platform trial to examine novel neoadjuvant immuno-oncology combinations for patients with resectable NSCLC, using major pathologic response (MPR) rate as the primary endpoint. Eighty-three patients received a single cycle of treatment: 26 received durvalumab (anti-PD-L1) monotherapy, 21 received durvalumab plus oleclumab (anti-CD73), 20 received durvalumab plus monalizumab (anti-NKG2A), and 16 received durvalumab plus danvatirsen (anti-STAT3 antisense oligonucleotide). MPR rates were higher for patients in the combination arms versus durvalumab alone. Safety profiles for the combinations were similar to those of durvalumab alone. Multiplatform immune profiling suggested that improved MPR rates in the durvalumab plus oleclumab and durvalumab plus monalizumab arms were associated with enhanced effector immune infiltration of tumors, interferon responses and markers of tertiary lymphoid structure formation, and systemic functional immune cell activation. SIGNIFICANCE: A neoadjuvant platform trial can rapidly generate clinical and translational data using candidate surrogate endpoints like MPR. In NeoCOAST, patients with resectable NSCLC had improved MPR rates after durvalumab plus oleclumab or monalizumab versus durvalumab alone and tumoral transcriptomic signatures indicative of augmented immune cell activation and function. See related commentary by Cooper and Yu, p. 2306. This article is featured in Selected Articles from This Issue, p. 2293.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsHumansNeoadjuvant TherapyAntibodies, Monoclonaldurvalumab

Identifiers

PMID37707791
PMCPMC10618740
OpenAlexW4386725951

What OpenQuestion holds

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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.