Evidence map›Paper›PMID 26227823›Full record

ReviewCancer gene therapy2015

Targeted radionuclide therapies for pancreatic cancer.

M Shah, R Da Silva, C Gravekamp, S K Libutti, T Abraham, E Dadachova

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer gene therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Molecular pharmaceutics · 2020
    Article
  6. B7-H3-targeted Radioimmunotherapy of Human Cancer.Current medicinal chemistry · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Nuclear medicine and biology · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Targeted Radionuclide Therapy of Human Tumors.International journal of molecular sciences · 2015
    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

6 authors at 1 institution in 1 country.

M ShahDepartments of Radiology, Albert Einstein College of Medicine, Bronx, NY, USA.
R Da SilvaDepartments of Radiology, Albert Einstein College of Medicine, Bronx, NY, USA.
C GravekampDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA.
S K Libutti1] Department of Surgery, Albert Einstein College of Medicine, Bronx, NY, USA [2] Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
T AbrahamDepartments of Radiology, Albert Einstein College of Medicine, Bronx, NY, USA.
E Dadachova1] Departments of Radiology, Albert Einstein College of Medicine, Bronx, NY, USA [2] Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA.
Albert Einstein College of Medicine · US

Funding

Project 4: New Approaches to Improving the Effectiveness of Radionuclide Targeted Treatments in Neuroendocrine TumorsP50CA174521 · NCI · UNIVERSITY OF IOWA · PI ODORISIO, THOMAS · 2015 to 2021
$13.2M
Treating pancreatic cancer with Listeria-32PR21CA199010 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GRAVEKAMP, CLAUDIA · 2015 to 2016
$400k
NCI NIH HHS P50 CA174521NCI NIH HHS R21 CA199010
6 · The paper itself

Abstract

Pancreatic malignancies, the fourth leading cause of cancer deaths, have an aggressive behavior with poor prognosis, resulting in a 5-year survival rate of only 4%. It is typically a silent malignancy until patients develop metastatic disease. Targeted radionuclide therapies of cancer such as radiolabeled peptides, which bind to the receptors overexpressed by cancer cells and radiolabeled antibodies to tumor-specific antigens provide a viable alternative to chemotherapy and external beam radiation of metastatic cancers. Multiple clinical trials of targeted radionuclide therapy of pancreatic cancer have been performed in the last decade and demonstrated safety and potential efficacy of radionuclide therapy for treatment of this formidable disease. Although a lot of progress has been made in treatment of pancreatic neuroendocrine tumors with radiolabeled (90)Y and (177)Lu somatostatin peptide analogs, pancreatic adenocarcinomas remain a major challenge. Novel approaches such as peptides and antibodies radiolabeled with alpha emitters, pre-targeting, bispecific antibodies and biological therapy based on the radioactive tumorlytic bacteria might offer a potential breakthrough in treatment of pancreatic adenocarcinomas.

Indexed as

AdenocarcinomaAnimalsAntibodies, MonoclonalCarcinoma, NeuroendocrineClinical Trials as TopicHumansListeriaMolecular Targeted TherapyOctreotideOrganometallic CompoundsPancreatic NeoplasmsRadioisotopesRadionuclide ImagingRadiopharmaceuticalsRhenium90Y-octreotate, DOTA(0)-Tyr(3)-Thr(8)-Antibodies, Monoclonalclivatuzumablutetium Lu 177 dotatateOctreotideOrganometallic CompoundsRadioisotopesRadiopharmaceuticalsRhenium

Identifiers

PMID26227823
PMCPMC4826043
OpenAlexW992368320

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.