Evidence map›Paper›PMID 29574039›Full record

Trial reportClinical immunology (Orlando, Fla.)2018

Phase Ib trial of folate binding protein (FBP)-derived peptide vaccines, E39 and an attenuated version, E39': An analysis of safety and immune response.

Timothy J Vreeland, Jennifer K Litton, Na Qiao, Anne V Philips, Gheath Alatrash, Diane F Hale, Doreen O Jackson, Kaitlin M Peace, Julia M Greene, John S Berry and 3 more

Registry-linked trialAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Clinical immunology (Orlando, Fla.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02019524 (Phase Ib Trial of Two Folate Binding Protein), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 38% 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.

NCT02019524 phase1completednot on this map

Phase Ib Trial of Two Folate Binding Protein (FBP) Peptide Vaccines (E39 and J65) in Breast and Ovarian Cancer Patients

TypeinterventionalSponsorCOL George Peoples, MD, FACSRan2013 to 2016Enrolled39ConditionsBreast Cancer, Ovarian CancerArmsE39 peptide vaccine, E39 vaccine then J65 vaccine, J65 vaccine then E39 vaccine
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. [Research Progress of Lung Cancer Vaccines].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Review
  5. Review
  6. Review
  7. Review
  8. 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

13 authors at 4 institutions in 1 country.

Timothy J VreelandDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St, Unit 1484, Houston, TX 77030, United States. Electronic address: tjvreeland@mdanderson.org.
Jennifer K LittonDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, 1155 Pressler St, Unit 1354, Houston, TX 77030, United States. Electronic address: jlitton@mdanderson.org.
Na QiaoDepartment of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St, Unit 1434, Houston, TX 77030, United States. Electronic address: nqiao@mdanderson.org.
Anne V PhilipsDepartment of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St, Unit 1434, Houston, TX 77030, United States. Electronic address: avphilips@mdanderson.org.
Gheath AlatrashDepartment of Stem Cell Transplantation and Cellular Therapy, The University of MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 423, Houston, TX 77030, United States. Electronic address: galatras@mdanderson.org.
Diane F HaleDepartment of Surgery, San Antonio Military Medical Center, 3551 Roger Brooke Dr, San Antonio, TX 78234, United States. Electronic address: diane.f.hale.mil@mail.mil.
Doreen O JacksonDepartment of Surgery, San Antonio Military Medical Center, 3551 Roger Brooke Dr, San Antonio, TX 78234, United States. Electronic address: Doreen.o.jackson.mil@mail.mil.
Kaitlin M PeaceDepartment of Surgery, San Antonio Military Medical Center, 3551 Roger Brooke Dr, San Antonio, TX 78234, United States. Electronic address: Kaitlin.m.peace.mil@mail.mil.
Julia M GreeneDepartment of Surgery, San Antonio Military Medical Center, 3551 Roger Brooke Dr, San Antonio, TX 78234, United States. Electronic address: Julia.m.greene.mil@mail.mil.
John S BerryDepartment of Surgery, Womack Army Medical Center, 2817 Reilly Rd, Fort Bragg, NC 28310, United States. Electronic address: john.s.berry.mil@mail.mil.
Guy T CliftonDepartment of Surgery, San Antonio Military Medical Center, 3551 Roger Brooke Dr, San Antonio, TX 78234, United States. Electronic address: Guy.t.clifton.mil@mail.mil.
George E PeoplesDepartment of Surgery, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Rd, Bethesda, MD 20814, United States.
Elizabeth A MittendorfDepartment of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St, Unit 1434, Houston, TX 77030, United States. Electronic address: emittendorf@bwh.harvard.edu.
The University of Texas MD Anderson Cancer Center · USBrooke Army Medical Center · USUniformed Services University of the Health Sciences · USWomack Army Medical Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

In this randomized phase Ib trial, we tested combining the E39 peptide vaccine with a vaccine created from E39', an attenuated version of E39. Patients with breast or ovarian cancer, who were disease-free after standard of care therapy, were enrolled and randomized to one of three arms. Arm EE received six E39 inoculations; arm EE' received three E39 inoculations followed by three E39'; and arm E'E received three E39' inoculations, followed by three E39. Within each arm, the first five patients received 500 μg of peptide and the remainder received 1000 μg. Patients were followed for toxicity, and immune responses were measured. This initial analysis after completion of the primary vaccination series has confirmed the safety of both vaccines. Immune analyses suggest incorporating the attenuated version of the peptide improves immune responses and that sequencing of E39 followed by E39' might produce the optimal immune response.

trial registrationNCT02019524.

Indexed as

AdultAgedAged, 80 and overBreast NeoplasmsCancer VaccinesFemaleFolate Receptors, GPI-AnchoredHumansHypersensitivity, DelayedMiddle AgedOvarian NeoplasmsT-Lymphocytes, CytotoxicVaccinationVaccines, AttenuatedVaccines, SubunitCancer VaccinesFolate Receptors, GPI-AnchoredVaccines, AttenuatedVaccines, SubunitActivation induced cell deathAttenuated vaccineBreast cancerFolate binding proteinOvarian cancerPeptide vaccine

Identifiers

PMID29574039
PMCPMC5988975
OpenAlexW2793778387

What OpenQuestion holds

Textmetadata
LicenceTDM
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.