Evidence map›Paper›PMID 29782599›Full record

ArticleEuropean journal of hybrid imaging2017

Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation.

Brittany Z Dashevsky, Chenpeng Zhang, Li Yan, Cindy Yuan, Lingyun Xiong, Yongmei Liu, Haiyan Liu, Feng-Ming Spring Kong, Yonglin Pu

Open access · goldAbstract read
In one paragraph

Article in European journal of hybrid imaging, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Incorporation of circulating tumor cells and whole-body metabolic tumor volume ofChinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2018
    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

9 authors at 6 institutions in 2 countries.

Brittany Z Dashevsky *1Department of Radiology, University Of Chicago, 5841 S. Maryland Ave. MC 2026, Chicago, IL 60637 USA.
Chenpeng Zhang2Department of Nuclear Medicine, RenJi Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Li Yan *3Department of Radiation Oncology, Linyi People's Hospital, Linyi, Shandong China.
Cindy Yuan1Department of Radiology, University Of Chicago, 5841 S. Maryland Ave. MC 2026, Chicago, IL 60637 USA.
Lingyun Xiong1Department of Radiology, University Of Chicago, 5841 S. Maryland Ave. MC 2026, Chicago, IL 60637 USA.
Yongmei LiuDepartment of Thoracic Oncology, China West University Hospital, Shichuan, Chengdu, China.
Haiyan Liu6Department of Nuclear Medicine, First Hospital of Shanxi Medical University and Molecular Imaging Precision Medical Collaborative Innovation Center, Shanxi Medical University, Taiyuan, 030001 Shanxi China.
Feng-Ming Spring Kong7Radiation Oncology, Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, USA.
Yonglin Pu1Department of Radiology, University Of Chicago, 5841 S. Maryland Ave. MC 2026, Chicago, IL 60637 USA.ORCID 0000-0002-9583-8185
University of Chicago · USIndiana University Health · USShandong University · CNShanghai Jiao Tong University · CNShanxi Medical University · CNSichuan University · CN

Funding

Developing a PET Volumetric Staging System for NSCLC: a Complement to TNM StagingR21CA181885 · NCI · UNIVERSITY OF CHICAGO · PI JIANG, YULEI, PU, YONGLIN · 2014 to 2015
$390k
NCI NIH HHS R21 CA181885
6 · The paper itself

Abstract

purposeTNM Stage 3B encompasses a wide range of primary tumor and nodal metastatic tumor burden. This study aimed to evaluate the prognostic value of quantitative FDG PET/CT parameters in patients with newly diagnosed Stage 3B Non-Small Cell Lung Cancer (NSCLC). MATERIALS AND

methodsInstitutional review board approved retrospective study identified patients diagnosed with Stage 3B NSCLC (8

resultsThe training set included 110 patients from center A with Stage 3B NSCLC. 78.2% of patients expired during follow-up. Median OS was 14 months. 1-year, 2-year, and 5-year OS was 56.5%, 34.6% and 13.9%, respectively. Univariate Cox regression analysis showed no significant difference in OS on the basis of age, gender, histology, ln(TLGwb), or ln(SUVmaxwb). ln(MTVwb) was positively associated with OS [hazard ratio (HR) of 1.23,

conclusionMTVwb is a prognostic marker for OS in patients with Stage 3B NSCLC, independent of age, gender, treatment, and tumor histology.

Indexed as

FDG, PET/CTLung cancerTumor volume

Identifiers

PMID29782599
PMCPMC5954780
OpenAlexW2762223816

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.