Evidence map›Paper›PMID 30370397›Full record

ArticleJCO precision oncology2018

Megakaryocyte Potentiating Factor as a Predictive Biomarker for Therapies Against Malignant Mesothelioma.

Liang Cao, Yunkai Yu, Anish Thomas, Jingli Zhang, Masanori Onda, Paul Meltzer, Raffit Hassan, Ira Pastan

Open access · greenAbstract read
In one paragraph

Article in JCO precision oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Observational
  2. Article
  3. Review
  4. Furin is not required for processing of mesothelin precursor protein.Biochimica et biophysica acta. Molecular cell research · 2021
    Article
  5. Circulating biomarkers in malignant pleural mesothelioma.Exploration of targeted anti-tumor therapy · 2020
    Review
  6. 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

8 authors at 1 institution in 1 country.

Liang CaoNational Cancer Institute, Bethesda, MD.
Yunkai YuNational Cancer Institute, Bethesda, MD.
Anish ThomasNational Cancer Institute, Bethesda, MD.
Jingli ZhangNational Cancer Institute, Bethesda, MD.
Masanori OndaNational Cancer Institute, Bethesda, MD.
Paul MeltzerNational Cancer Institute, Bethesda, MD.
Raffit Hassan *National Cancer Institute, Bethesda, MD.
Ira Pastan *National Cancer Institute, Bethesda, MD.
National Cancer Institute · US

Funding

Design, Develop, Validate, and Implement Biomarkers for Clinical InvestigationsZICBC010981 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HESELMEYER, KERSTIN · 2009 to 2025
$11.7M
Predictive Biomarkers and Mechanism of Action for Anti-IGF1R Agents for CancerZ01BC011048 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CAO, LIANG · 2008 to 2008
$317k
Design, Develop, Validate, and Implement Biomarkers for Clinical InvestigationsZ01BC010981 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CAO, LIANG · 2008 to 2008
$211k
Intramural NIH HHS Z01 BC010981Intramural NIH HHS Z01 BC011048
6 · The paper itself

Abstract

purposeEffective biomarkers for malignant mesothelioma (MM) are needed for clinical management and the development of mesothelin-targeted therapies. We evaluated serum megakaryocyte potentiating factor (MPF) as a biomarker predictive of treatment outcome in patients with MM and for developing mesothelin-targeted therapies. MATERIALS AND

methodsSerial serum samples from patients with MM in two clinical trials of an antimesothelin immunotoxin were tested with our clinically validated MPF assay. Correlative studies were performed to determine the test effectiveness in treatment monitoring and outcome prediction. MPF was further evaluated for an association with response to an antimesothelin therapy and for disease monitoring.

resultsThere was a significant reduction of serum MPF in patients with elevated baseline and radiologic response, with an average change from -52% to -78% after one to six cycles. Using a -50% change as the cutoff, patients with MM with positive MPF response had significantly improved progression-free survival (

conclusionAt a cutoff of -50% change after receiving systemic therapies, a reduction in MPF was associated with improved clinical outcome, both progression-free survival and overall survival. An elevated baseline serum MPF was associated with a response to an antimesothelin therapy in patients with refractory MM; however, this finding needs to be confirmed in another study.

Identifiers

PMID30370397
PMCPMC6201260
OpenAlexW2800390367

What OpenQuestion holds

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Registered trials

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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.