Evidence map›Paper›PMID 28923084›Full record

Trial reportJournal for immunotherapy of cancer2017

Viral based vaccine TG4010 induces broadening of specific immune response and improves outcome in advanced NSCLC.

Caroline Tosch, Bérangère Bastien, Luc Barraud, Benoit Grellier, Virginie Nourtier, Murielle Gantzer, Jean Marc Limacher, Eric Quemeneur, Kaïdre Bendjama, Xavier Préville

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal for immunotherapy of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01383148 (A Phase IIB/III Randomized, Double-blind, Placebo Controlled Study Comparing First Line Therapy With or Without TG4010 Immunotherapy Product in Patients With Stage IV Non-Small Cell Lung Cancer), which is not on this map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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.

NCT01383148 phase2 / phase3terminatednot on this map

A Phase IIB/III Randomized, Double-blind, Placebo Controlled Study Comparing First Line Therapy With or Without TG4010 Immunotherapy Product in Patients With Stage IV Non-Small Cell Lung Cancer (NSCLC)

TypeinterventionalSponsorTransgeneRan2012 to 2016Enrolled222ConditionsNon-Small-Cell Lung CarcinomaArmsTG4010, placebo
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Therapeutic vaccines for advanced non-small cell lung cancer.The Cochrane database of systematic reviews · 2024
    Pooled it
  2. Trial
  3. Therapeutic vaccines for NSCLC: From mechanisms to clinical translation.Chinese medical journal pulmonary and critical care medicine · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. MUC1 in the upper-lower airway inflammatory continuum: an endotype-centered perspective.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  8. Article
  9. The next generation of immunotherapies for lung cancers.Nature reviews. Clinical oncology · 2025
    Review
  10. Review
  11. Review
  12. The progress of tumor vaccines clinical trials in 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 · 2025
    Review
  13. Cancer vaccines: current status and future directions.Journal of hematology & oncology · 2025
    Review
  14. Review
  15. Therapeutic Vaccination in Lung Cancer: Past Attempts, Current Approaches and Future Promises.Journal of respiratory biology and translational medicine · 2025
    Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review
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

10 authors at 1 institution in 2 countries.

Caroline ToschTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Bérangère BastienTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Luc BarraudTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Benoit GrellierTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Virginie NourtierTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Murielle GantzerTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Jean Marc LimacherTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Eric QuemeneurTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Kaïdre BendjamaTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France. bendjama@transgene.fr.ORCID 0000-0003-2185-9116
Xavier PrévilleTransgene SA, 400 Bld Gonthier d'Andernach, Parc d'Innovation, CS80166, 67405, Illkirch Graffenstaden, Cedex, France.
Transgene (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvanced non-small cell lung cancer patients receiving TG4010, a therapeutic viral vaccine encoding human Mucin 1 and interleukin-2 in addition to standard chemotherapy, displayed longer overall survival in comparison to that of patients treated with standard chemotherapy alone. Our study intended to establish the association between overall survival and vaccine-induced T cell responses against tumor associated antigens (TAA) targeted by the vaccine.

methodThe TIME trial was a placebo-controlled, randomized phase II study aimed at assessing efficacy of TG4010 with chemotherapy in NSCLC. 78 patients from the TIME study carrying the HLA-A02*01 haplotype were analyzed using combinatorial encoding of MHC multimers to detect low frequencies of cellular immune responses to TG4010 and other unrelated TAA.

resultsWe report that improvement of survival under TG4010 treatment correlated with development of T cell responses against MUC1. Interestingly, responses against MUC1 were associated with broadening of CD8 responses against non-targeted TAA, thus demonstrating induction of epitope spreading.

conclusionOur results support the causality of specific T-cell response in improved survival in NSCLC. Additionally, vaccine induced epitope spreading to other TAA participates to the enrichment of the diversity of the anti-tumor response. Hence, TG4010 appears as a useful therapeutic option to maximize response rate and clinical benefit in association with other targeted immuno-modulators.

trial registrationRegistered on ClinicalTrials.gov under identifier NCT01383148 on June 23rd, 2011.

Indexed as

Antigens, NeoplasmCancer VaccinesCarcinoma, Non-Small-Cell LungDouble-Blind MethodHLA-A2 AntigenHumansLung NeoplasmsMembrane GlycoproteinsMucin-1Survival AnalysisT-LymphocytesTreatment OutcomeAntigens, NeoplasmCancer VaccinesHLA-A*02:01 antigenHLA-A2 AntigenMembrane GlycoproteinsMUC1 protein, humanMucin-1TG4010Cancer vaccineLung cancerT cell responseTumor associated antigenViral vaccine

Identifiers

PMID28923084
PMCPMC5604422
OpenAlexW2752478591

What OpenQuestion holds

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LicenceCC BY
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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.