Evidence map›Paper›PMID 23302905›Full record

ReviewCancer control : journal of the Moffitt Cancer Center2013

Immunotherapy for gastrointestinal malignancies.

Paul G Toomey, Nasreen A Vohra, Tomar Ghansah, Amod A Sarnaik, Shari A Pilon-Thomas

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer control : journal of the Moffitt Cancer Center, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. mFrontiers in molecular biosciences · 2020
    Article
  10. Review
  11. Article
  12. Review
  13. Immunotherapy in Gastrointestinal Cancers.BioMed research international · 2017
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Current status of predictive biomarkers for neoadjuvant therapy in esophageal cancer.World journal of gastrointestinal pathophysiology · 2014
    Review
  19. Review
  20. Changes in T lymphocyte subsets in mice with CT26 colon tumors after treatment with donor lymphocyte infusion.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    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

5 authors at 1 institution in 1 country.

Paul G ToomeyDepartment of Surgery, USF Health Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
Nasreen A Vohra
Tomar Ghansah
Amod A Sarnaik
Shari A Pilon-Thomas
Moffitt Cancer Center · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

backgroundGastrointestinal (GI) cancers are the most common human tumors encountered worldwide. The majority of GI cancers are unresectable at the time of diagnosis, and in the subset of patients undergoing resection, few are cured. There is only a modest improvement in survival with the addition of modalities such as chemotherapy and radiation therapy. Due to an increasing global cancer burden, it is imperative to integrate alternative strategies to improve outcomes. It is well known that cancers possess diverse strategies to evade immune detection and destruction. This has led to the incorporation of various immunotherapeutic strategies, which enable reprogramming of the immune system to allow effective recognition and killing of GI tumors.

methodsA review was conducted of the results of published clinical trials employing immunotherapy for esophageal, gastroesophageal, gastric, hepatocellular, pancreatic, and colorectal cancers.

resultsMonoclonal antibody therapy has come to the forefront in the past decade for the treatment of colorectal cancer. Immunotherapeutic successes in solid cancers such as melanoma and prostate cancer have led to the active investigation of immunotherapy for GI malignancies, with some promising results.

conclusionsTo date, monoclonal antibody therapy is the only immunotherapy approved by the US Food and Drug Administration for GI cancers. Initial trials validating new immunotherapeutic approaches, including vaccination-based and adoptive cell therapy strategies, for GI malignancies have demonstrated safety and the induction of antitumor immune responses. Therefore, immunotherapy is at the forefront of neoadjuvant as well as adjuvant therapies for the treatment and eradication of GI malignancies.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedBevacizumabCancer VaccinesCetuximabCombined Modality TherapyGastrointestinal NeoplasmsHumansImmunotherapyImmunotherapy, AdoptivePanitumumabTrastuzumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBevacizumabCancer VaccinesCetuximabPanitumumabTrastuzumab

Identifiers

PMID23302905
PMCPMC4761871
OpenAlexW2185633646

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.