Evidence map›Paper›PMID 19456205›Full record

ReviewExpert opinion on biological therapy2009

Cellular immunotherapy for ovarian cancer.

Martin J Cannon, Timothy J O'Brien

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on biological therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Multifaceted therapeutic targeting of ovarian peritoneal carcinomatosis through virus-induced immunomodulation.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  5. Immunotherapy in ovarian cancer.Human vaccines & immunotherapeutics · 2012
    Review
  6. Immunotherapy for ovarian cancer: what's next?Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Review
  7. Article
  8. Whole tumor antigen vaccines.Seminars in immunology · 2010
    Review
  9. Article
  10. Review
  11. Immunotherapy of cancer in 2012.CA: a cancer journal for clinicians
    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

2 authors at 1 institution in 1 country.

Martin J CannonUniversity of Arkansas for Medical Sciences, Department of Microbiology and Immunology, 4301 West Markham, Little Rock, AR 72205, USA. mjcannon@uams.edu
Timothy J O'Brien
University of Arkansas for Medical Sciences · US

Funding

Novel target antigens for ovarian cancer immunotherapyR01CA098927 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI CANNON, MARTIN J. · 2004 to 2007
$1.0M
Dendritic cell immunotherapy for ovarian cancerR41CA108257 · NCI · DCV TECHNOLOGIES, INC. · PI CANNON, MARTIN J · 2005 to 2005
$67k
NCI NIH HHS CA 098927NCI NIH HHS CA 108257NCI NIH HHS R01 CA098927NCI NIH HHS R41 CA108257
6 · The paper itself

Abstract

backgroundOvarian cancer is frequently diagnosed at an advanced stage, and although initially responsive to surgery and chemotherapy, has a high rate of recurrence and mortality. Cellular immunotherapy may offer the prospect of treatment to prevent or delay recurrent metastatic disease.

objectiveTo provide an overview of current innovations in cellular immunotherapy for ovarian cancer, with an emphasis on dendritic cell vaccination and adoptive T-cell immunotherapy.

methodsThree key areas are explored in this review: first, an appraisal of the current state of the art of cellular immunotherapy for treatment of ovarian cancer; second, a discussion of the immunological defenses erected by ovarian cancer to prevent immunological attack, with an emphasis on the role of tumor-associated regulatory T cells; and third, an exploration of innovative techniques that may enhance the ability of cellular immunotherapy to overcome ovarian tumor-associated immune suppression. RESULTS/

conclusionOvarian cancer is recognized as a paradigm for tumor-associated immune suppression. Innovative approaches for antagonism of tumor-associated regulatory T-cell infiltration and redirection of self antigen-driven regulatory T-cell activation may provide the key to development of future strategies for cellular immunotherapy against ovarian cancer.

Indexed as

Adoptive TransferFemaleHumansOvarian NeoplasmsT-Lymphocytes, Regulatory

Identifiers

PMID19456205
PMCPMC2718679
OpenAlexW2063940197

What OpenQuestion holds

Textmetadata
LicenceTDM
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.