Evidence map›Paper›PMID 33016924›Full record

Trial reportThe Journal of clinical investigation2020

mRNA vaccine-induced neoantigen-specific T cell immunity in patients with gastrointestinal cancer.

Gal Cafri, Jared J Gartner, Tal Zaks, Kristen Hopson, Noam Levin, Biman C Paria, Maria R Parkhurst, Rami Yossef, Frank J Lowery, Mohammad S Jafferji and 9 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03480152 (A Phase I/II Trial to Evaluate the Safety and Immunogenicity of a Messenger RNA), which is not on this map. Cited by 293 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
293citing papers in PubMed, 2 pooled it
18.3field-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.

NCT03480152 phase1 / phase2terminatednot on this map

A Phase I/II Trial to Evaluate the Safety and Immunogenicity of a Messenger RNA (mRNA)-Based, Personalized Cancer Vaccine Against Neoantigens Expressed by the Autologous Cancer

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2018 to 2019Enrolled5ConditionsMelanoma, Colon Cancer, Gastrointestinal Cancer, Genitourinary CancerArmsNational Cancer Institute (NCI)-4650, a messenger ribonucleic acid (mRNA)-based, Personalized Cancer Vaccine
3 · Its place in the literature

Who cites it

293 citing papers in PubMed, 2 syntheses or guidelines pooled it, 397 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. [Novel therapeutic strategies for liver metastases driven by the common microenvironment].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
    Review
  6. Predicting Neoantigen Immunogenicity frombioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Precision Targeting ofInternational journal of molecular sciences · 2026
    Review
  14. Article
  15. Review
  16. Review
  17. Article
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  19. Review
  20. Review

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

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

19 authors at 3 institutions in 2 countries.

Gal CafriSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Jared J GartnerSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Tal ZaksModerna Inc., Cambridge, Massachusetts, USA.
Kristen HopsonModerna Inc., Cambridge, Massachusetts, USA.
Noam LevinSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Biman C PariaSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Maria R ParkhurstSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Rami YossefSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Frank J LowerySurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Mohammad S JafferjiSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Todd D PrickettSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Stephanie L GoffSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Christine T McGowanSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Samantha SeitterSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Mackenzie L ShindorfSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Anup ParikhSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Praveen D ChataniSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Paul F RobbinsSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
Steven A RosenbergSurgery Branch, National Cancer Institute (NCI), NIH, Bethesda, Maryland, USA.
National Cancer Institute · USModerna Therapeutics (United States) · USSheba Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUNDTherapeutic vaccinations against cancer have mainly targeted differentiation antigens, cancer-testis antigens, and overexpressed antigens and have thus far resulted in little clinical benefit. Studies conducted by multiple groups have demonstrated that T cells recognizing neoantigens are present in most cancers and offer a specific and highly immunogenic target for personalized vaccination.METHODSWe recently developed a process using tumor-infiltrating lymphocytes to identify the specific immunogenic mutations expressed in patients' tumors. Here, validated, defined neoantigens, predicted neoepitopes, and mutations of driver genes were concatenated into a single mRNA construct to vaccinate patients with metastatic gastrointestinal cancer.RESULTSThe vaccine was safe and elicited mutation-specific T cell responses against predicted neoepitopes not detected before vaccination. Furthermore, we were able to isolate and verify T cell receptors targeting KRASG12D mutation. We observed no objective clinical responses in the 4 patients treated in this trial.CONCLUSIONThis vaccine was safe, and potential future combination of such vaccines with checkpoint inhibitors or adoptive T cell therapy should be evaluated for possible clinical benefit in patients with common epithelial cancers.TRIAL REGISTRATIONPhase I/II protocol (NCT03480152) was approved by the IRB committee of the NIH and the FDA.FUNDINGCenter for Clinical Research, NCI, NIH.

Indexed as

Antigens, NeoplasmCancer VaccinesGastrointestinal NeoplasmsImmunity, CellularMutation, MissenseProto-Oncogene Proteins p21(ras)RNA, MessengerAmino Acid SubstitutionFemaleHumansMaleT-LymphocytesAntigens, NeoplasmCancer VaccinesKRAS protein, humanProto-Oncogene Proteins p21(ras)RNA, MessengerCancer immunotherapyOncologyVaccines

Identifiers

PMID33016924
PMCPMC7598064
OpenAlexW3091061098

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.