Evidence map›Paper›PMID 32732224›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Stimulation of Oncogene-Specific Tumor-Infiltrating T Cells through Combined Vaccine and αPD-1 Enable Sustained Antitumor Responses against Established HER2 Breast Cancer.

Erika J Crosby, Chaitanya R Acharya, Anthony-Fayez Haddad, Christopher A Rabiola, Gangjun Lei, Jun-Ping Wei, Xiao-Yi Yang, Tao Wang, Cong-Xiao Liu, Kay U Wagner and 16 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03632941 (A Phase II Randomized Study to Evaluate the Immunologic and Antitumor Activity of Concurrent VRP-HER2 Vaccination and Pembrolizumab for Patients With Advanced HER2-overexpressing Breast Cancer), which is not on this map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 9% 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.

NCT03632941 phase2terminatednot on this map

A Phase II Randomized Study to Evaluate the Immunologic and Antitumor Activity of Concurrent VRP-HER2 Vaccination and Pembrolizumab for Patients With Advanced HER2-overexpressing Breast Cancer

TypeinterventionalSponsorHerbert LyerlyRan2019 to 2024Enrolled8ConditionsBreast Cancer, HER2+ Breast CancerArmsVRP-HER2, Pembrolizumab
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Restoring the CD226 in CD8Cell death & disease · 2026
    Article
  4. Enhanced efficacy of a next-generation EEEV self-replicating RNA platform for combination cancer immunotherapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Vaccines targetingHuman vaccines & immunotherapeutics · 2024
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Beyond Neoantigens: Antigens Derived from Tumor Drivers as Cancer Vaccine Targets.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    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

26 authors at 5 institutions in 2 countries.

Erika J CrosbyDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.ORCID 0000-0002-4872-6711
Chaitanya R AcharyaDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.ORCID 0000-0001-7149-1749
Anthony-Fayez HaddadDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.ORCID 0000-0001-6814-376X
Christopher A RabiolaDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.
Gangjun LeiDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.
Jun-Ping WeiDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.
Xiao-Yi YangDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.
Tao WangDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.
Cong-Xiao LiuDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.
Kay U WagnerDepartment of Oncology, Wayne State University, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan.ORCID 0000-0002-5081-0226
William J MullerDepartments of Biochemistry and Medicine, Goodman Cancer Center, McGill University, Montreal, Quebec.
Lewis A ChodoshDepartment of Cancer Biology, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-1027-8674
Gloria BroadwaterDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.
Terry HyslopDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.
Jonathan H ShepherdLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Daniel P HollernLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Xiaping HeLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0001-9464-7910
Charles M PerouLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0001-9827-2247
Shengjie ChaiLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Benjamin K AshbyLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Benjamin G VincentLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0002-1762-2282
Joshua C SnyderDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.
Jeremy ForceDepartment of Medicine, Duke University, Durham, North Carolina.
Michael A MorseDepartment of Medicine, Duke University, Durham, North Carolina.
Herbert K LyerlyDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina.ORCID 0000-0002-0063-4770
Zachary C HartmanDepartment of Surgery, Division of Surgical Sciences, Duke University, Durham North Carolina. Zachary.hartman@duke.edu.ORCID 0000-0001-6549-8207
Duke University · USUniversity of North Carolina at Chapel Hill · USMcGill University · CAThe Barbara Ann Karmanos Cancer Institute · USUniversity of Pennsylvania · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Viral Oncology Training GrantT32CA009111 · NCI · DUKE UNIVERSITY · PI LUFTIG, MICAH A. · 1985 to 2023
$8.9M
Clinical Oncology Research Career Development ProgramK12CA100639 · NCI · DUKE UNIVERSITY · PI LYERLY, HERBERT KIM · 2004 to 2013
$8.0M
In Vivo Ras-induced Senescence and TumorigenesisR01CA098371 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LEWIS A CHODOSH · 2003 to 2026
$7.4M
Enabling effective anti-tumor immunity from targeted antibodies through dual innate and adaptive immune checkpoint blockade in non-immunogenic cancersR01CA238217 · NCI · DUKE UNIVERSITY · PI HARTMAN, ZACHARY CONRAD · 2020 to 2024
$2.4M
Supplemental Funds for K22 Establishing the molecular and cellular mechanisms of Lgr5 signaling for controlling cancer stem cell behaviorK22CA212058 · NCI · DUKE UNIVERSITY · PI SNYDER, JOSHUA CLAIR · 2017 to 2020
$622k
CIHR FND-148373NCI NIH HHS K12 CA100639NCI NIH HHS K22 CA212058NCI NIH HHS P30 CA016086NCI NIH HHS R01 CA098371NCI NIH HHS R01 CA238217NCI NIH HHS T32 CA009111
6 · The paper itself

Abstract

purposeDespite promising advances in breast cancer immunotherapy, augmenting T-cell infiltration has remained a significant challenge. Although neither individual vaccines nor immune checkpoint blockade (ICB) have had broad success as monotherapies, we hypothesized that targeted vaccination against an oncogenic driver in combination with ICB could direct and enable antitumor immunity in advanced cancers. EXPERIMENTAL

designOur models of HER2

resultsWe found that only vaccination targeting HER2Δ16, a driver of oncogenicity and HER2-therapeutic resistance, could elicit significant antitumor responses, while vaccines targeting a nondriver tumor-specific antigen or tumor neoepitopes did not. Vaccine-induced HER2-specific CD8

conclusionsCombining oncogenic driver targeted vaccines with selective ICB offers a rational paradigm for precision immunotherapy, which we are clinically evaluating in a phase II trial (NCT03632941).

Indexed as

AnimalsAntigens, NeoplasmBreast NeoplasmsCancer VaccinesCD8-Positive T-LymphocytesCell Line, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansImmune Checkpoint InhibitorsImmunotherapyLymphocytes, Tumor-InfiltratingMammary Neoplasms, ExperimentalMiceMice, TransgenicProgrammed Cell Death 1 ReceptorAntigens, NeoplasmCancer VaccinesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorVaccines, Combined

Identifiers

PMID32732224
PMCPMC7483405
OpenAlexW3046570011

What OpenQuestion holds

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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.