Evidence map›Paper›PMID 11676282›Full record

ReviewHematology/oncology clinics of North America2001

Cancer vaccines.

R F Rousseau, C Hirschmann-Jax, S Takahashi, M K Brenner

Abstract readReview
In one paragraph

Review in Hematology/oncology clinics of North America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Mesoporous Silica Materials as an Emerging Tool for Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  5. Review
  6. Review
  7. 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

4 authors.

R F RousseauCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas, USA.
C Hirschmann-Jax
S Takahashi
M K Brenner

Funding

Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

Attempts to generate an anticancer immune response in vivo in patients with cancer have taken several forms. Although to date there have been relatively few published studies describing the effects of the approach in hematologic malignancy, that circumstance is expected to change rapidly during the next few years. In solid tumors, it is not known which, if any, of the approaches being explored will be able to produce responses of sufficient effectiveness and duration to be of general clinical value. Despite the documented increase in survival of patients developing an immune response to tumor immunization, no randomized clinical trial has been entirely convincing. As knowledge of the molecular basis of the immune response and of the immune defenses used by cancer cells improves, it is reasonable to expect to see increasing benefits from tumor vaccines, which are likely to complement, long before they replace, conventional therapies.

Indexed as

Cancer VaccinesAntigen PresentationAntigens, NeoplasmB-Lymphocyte SubsetsDendritic CellsEpitopesGenetic EngineeringHematologic NeoplasmsHLA AntigensHumansImmunizationImmunization, PassiveImmunologic Deficiency SyndromesImmunologic SurveillanceImmunotherapyModels, ImmunologicalAntigens, NeoplasmCancer VaccinesEpitopesHLA AntigensPeptide FragmentsPolynucleotidesReceptors, Antigen, T-Cell

Identifiers

PMID11676282
PMCPMC6361626

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.