Evidence map›Paper›PMID 32135247›Full record

ReviewPharmacological research2020

Developing effective combination therapy for pancreatic cancer: An overview.

Aubrey L Miller, Patrick L Garcia, Karina J Yoon

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacological research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
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  13. The ethyl acetate extract ofSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
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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

3 authors at 1 institution in 1 country.

Aubrey L MillerDepartment of Pharmacology and Toxicology, University of Alabama at Birmingham, Birmingham AL, 35294 USA.
Patrick L GarciaDepartment of Pharmacology and Toxicology, University of Alabama at Birmingham, Birmingham AL, 35294 USA.
Karina J YoonDepartment of Pharmacology and Toxicology, University of Alabama at Birmingham, Birmingham AL, 35294 USA. Electronic address: kyoon@uab.edu.
University of Alabama at Birmingham · US

Funding

Developing novel combination therapies for pancreatic cancerR01CA208272 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YOON, KARINA J · 2017 to 2021
$1.7M
NCI NIH HHS R01 CA208272
6 · The paper itself

Abstract

Pancreatic cancer is a fatal disease. The five-year survival for patients with all stages of this tumor type is less than 10%, with a majority of patients dying from drug resistant, metastatic disease. Gemcitabine has been a standard of care for the treatment of pancreatic cancer for over 20 years, but as a single agent gemcitabine is not curative. Since the only therapeutic option for the over 80 percent of pancreatic cancer patients ineligible for surgical resection is chemotherapy with or without radiation, the last few decades have seen a significant effort to develop effective therapy for this disease. This review addresses preclinical and clinical efforts to identify agents that target molecular characteristics common to pancreatic tumors and to develop mechanism-based combination approaches to therapy. Some of the most promising combinations include agents that inhibit transcription dependent on BET proteins (BET bromodomain inhibitors) or that inhibit DNA repair mediated by PARP (PARP inhibitors).

Indexed as

AcetylationAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBromodomain Containing ProteinsDeoxycytidineDNA DamageGemcitabineHistonesHumansPancreatic NeoplasmsProteinsAntineoplastic Agentsbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsDeoxycytidineGemcitabineHistonesProteinsAZD6738 (PubChem CID: 54761306)BET bromodomain inhibitorsBevacizumab (PubChem SID: 46504473)Cetuximab (PubChem SID: 46507042)Erlotinib (PubChem CID: 176870)GemcitabineGemcitabine (PubChem CID: 60750)JQ1 (PubChem CID: 49871818)MK-8776 (PubChem CID: 46239015)Nivolumab (PubChem SID: 178103907)Olaparib (PubChem CID: 23725625)Pancreatic cancerPARP inhibitorsVorinostat (PubChem CID: 5311)

Identifiers

PMID32135247
PMCPMC7365261
OpenAlexW3009108530

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.