Evidence map›Paper›PMID 17981543›Full record

ReviewFrontiers in bioscience : a journal and virtual library2008

Chemotherapy and tumor immunity: an unexpected collaboration.

Leisha A Emens

Open access · bronzeAbstract readReview
In one paragraph

Review in Frontiers in bioscience : a journal and virtual library, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Immunotherapy in breast cancer.Journal of carcinogenesis · 2019
    Review
  9. Article
  10. Article
  11. Polysaccharides Extracted fromInternational journal of molecular sciences · 2018
    Article
  12. Review
  13. Review
  14. Changes in the immune cell population and cell proliferation in peripheral blood after gemcitabine-based chemotherapy for pancreatic cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2014
    Article
  15. Review
  16. Optimal treatment strategy for a tumor model under immune suppression.Computational and mathematical methods in medicine · 2014
    Article
  17. Review
  18. Consensus report of the national cancer institute clinical trials planning meeting on pancreas cancer treatment.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2009
    Review
  19. Article
  20. Pretreatment with cisplatin enhances E7-specific CD8+ T-Cell-mediated antitumor immunity induced by DNA vaccination.Clinical cancer research : an official journal of the American Association for Cancer Research · 2008
    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

1 author at 1 institution in 1 country.

Leisha A EmensDepartment of Oncology, The Johns Hopkins University and the Sidney Kimmel Comprehensive Cancer Center, 1650 Orleans Street, Room 4M90, Bunting Blaustein Cancer Research Building, Baltimore, MD 21231-1000, USA. emensle@jhmi.edu
Sidney Kimmel Comprehensive Cancer Center · US

Funding

SYNERGISTIC CHEMOTHERAPY HER2/NEU VACCINES--BREAST CANCEU19CA072108 · NCI · JOHNS HOPKINS UNIVERSITY · PI JAFFEE, ELIZABETH MARION · 1996 to 2003
$3.7M
CHEMOIMMUNOTHERAPY FOR BREAST CANCER TREATMENTK23CA098498 · NCI · JOHNS HOPKINS UNIVERSITY · PI EMENS, LEISHA A · 2003 to 2006
$554k
NCI NIH HHS 1K23 CA098498NCI NIH HHS K23 CA098498NCI NIH HHS U19 CA072108NCI NIH HHS U19CA72108
6 · The paper itself

Abstract

Chemotherapy directly targets the transformed tumor cell, and has long been a key component of therapy for most early and advanced cancers. However, its utility is ultimately limited by unavoidable toxicity to normal tissues, and by drug resistance pathways deeply embedded within the biology of the tumor cell itself. These limitations strongly argue for innovative strategies to treat and manage cancer. Engaging the power of the patient's own immune system is a highly attractive way to complement the activity of standard cancer treatment. Tumor vaccines offer the potential for preventing cancer in those at high risk for disease development, preventing relapse in those diagnosed with early cancer, and treating advanced disease. Notably, the barriers to tumor vaccine efficacy are distinct from the limitations of combination chemotherapy. The ability of vaccines to induce a response robust enough to mediate tumor rejection is limited by the extent of disease burden, the suppressive effect of the local tumor micronenvironment, and multiple layers of systemic immune tolerance established to keep the immune response turned off. Chemotherapy can be used with tumor vaccines in unexpected ways, breaking down these barriers and unleashing the full potential of the antitumor immune response.

Indexed as

AnimalsAntineoplastic AgentsCombined Modality TherapyHumansImmune SystemImmune ToleranceImmunotherapyMiceNeoplasmsAntineoplastic Agents

Identifiers

PMID17981543
PMCPMC3086378
OpenAlexW1631276405

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.