Evidence map›Paper›PMID 17517052›Full record

Trial reportCancer science2007

Clinical trial of autologous formalin-fixed tumor vaccine for glioblastoma multiforme patients.

Eiichi Ishikawa, Koji Tsuboi, Tetsuya Yamamoto, Ai Muroi, Shingo Takano, Takao Enomoto, Akira Matsumura, Tadao Ohno

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Cancer science, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 22% 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

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 83 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Glioblastoma vaccine tumor therapy research progress.Chinese neurosurgical journal · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Vaccination in the immunotherapy of glioblastoma.Human vaccines & immunotherapeutics · 2018
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  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

8 authors at 4 institutions in 1 country.

Eiichi IshikawaDepartment of Neurosurgery, Ibaraki Prefectural Central Hospital, Kasama, Ibaraki 309-1793, Japan.
Koji Tsuboi
Tetsuya Yamamoto
Ai Muroi
Shingo Takano
Takao Enomoto
Akira Matsumura
Tadao Ohno
University of Tsukuba · JPUniversity of Tsukuba Hospital · JPIbaraki Prefectural Central Hospital · JPWaseda University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A pilot study was performed to investigate the safety and feasibility of autologous formalin-fixed tumor vaccines (AFTV) and the clinical responses to these vaccines by glioblastoma multiforme (GBM) patients. Twelve primary GBM patients were recruited. Eight had recurrent disease while four had been treated for primary disease but retained a visible tumor mass. AFTV were prepared from formalin-fixed and/or paraffin-embedded tumor tissue obtained upon surgery and premixed with original adjuvant materials. The patients were given three five-site intradermal inoculations at weekly intervals. A delayed-type hypersensitivity test was performed before and after each vaccination. In addition, the tumor tissues were subjected to immunohistochemical analysis to determine whether MIB-1, p53, and major histocompatibility complex (MHC) class-I complex expression could predict the response to the treatment. The treatment was well tolerated, with only local erythema, induration, and low-grade fever being reported. Of the 12 patients, one showed a complete response, one showed a partial response, two showed minor responses, one had stable disease, and seven exhibited progressive disease. The median survival period was 10.7 months from the initiation of the AFTV treatment but three of the five responders survived for 20 months or more after AFTV inoculation. Low p53 and high MHC class-I expression by the tumor may help predict the efficacy of this therapy. Thus, the AFTV is safe and feasible, and could significantly improve the outcome of GBM. Further clinical investigations to confirm this are highly desirable.

Indexed as

Cancer VaccinesAdolescentAdultAgedBrain NeoplasmsFeasibility StudiesFemaleFixativesGlioblastomaHumansImmunohistochemistryMagnetic Resonance ImagingMaleMiddle AgedPilot ProjectsPredictive Value of TestsCancer VaccinesFixatives

Identifiers

PMID17517052
PMCPMC11158799
OpenAlexW1995172058

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.