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Thoracic radiation-induced pleural effusion and risk factors in patients with lung cancer

  • Jing Zhao
    ,
  • Regina M. Day
    ,
  • JianYue Jin
    ,
  • Leslie Quint
    ,
  • Hadyn T Williams
    ,
  • Catherine Lowrie Ferguson
*Corresponding author for this work
  • Huazhong University of Science and Technology
    ,
  • Medical College of Georgia
    ,
  • Uniformed Services University of the Health Sciences
    ,
  • ,
  • University of Michigan, Ann Arbor
    ,
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

The risk factors and potential practice implications of radiation-induced pleural effusion (RIPE) are undefined. This study examined lung cancer patients treated with thoracic radiation therapy (TRT) having follow-up computed tomography (CT) or 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT. Increased volumes of pleural effusion after TRT without evidence of tumor progression was considered RIPE. Parameters of lung dose-volume histogram including percent volumes irradiated with 5-55 Gy (V5-V55) and mean lung dose (MLD) were analyzed by receiver operating characteristic analysis. Clinical and treatment-related risk factors were detected by univariate and multivariate analyses. 175 out of 806 patients receiving TRT with post-treatment imaging were included. 51 patients (24.9%) developed RIPE; 40 had symptomatic RIPE including chest pain (47.1%), cough (23.5%) and dyspnea (35.3%). Female (OR = 0.380, 95% CI: 0.156-0.926, p = 0.033) and Caucasian race (OR = 3.519, 95% CI: 1.327-9.336, p = 0.011) were significantly associated with lower risk of RIPE. Stage and concurrent chemotherapy had borderline significance (OR = 1.665, p = 0.069 and OR = 2.580, p = 0.080, respectively) for RIPE. Patients with RIPE had significantly higher whole lung V5-V40, V50 and MLD. V5 remained as a significant predictive factor for RIPE and symptomatic RIPE (p = 0.007 and 0.022) after adjusting for race, gender and histology. To include, the incidence of RIPE is notable. Whole lung V5 appeared to be the most significant independent risk factor for symptomatic RIPE.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 97623-97632 (10 pages)

Journal (Volume, Issue Number)

Oncotarget (Volume 8, Issue 57)

Publication milestones

  • Published - 2017

Publication status

Published - 2017

ISSN

1949-2553

Publication IDs

  • Scopus: 85033781052
  • PubMed: 29228638

Publication metrics

Metrics

Scopus
citations
Fractional count
4
Fractional count
0.36
Fractional count
7
Fractional count
0.64
Fractional count
4
Fractional count
1
SciVal
FWCI
0.31
SciVal
Author count
11
SciVal
citations
4
SciVal
Paper percentile
56

PlumX, opens in new tab

Captures
22
Citation count
13

Funding Details

This work was supported in part by NIH/NCI R01CA142840 (Kong).
FunderFunding number
NCI, NIH
R01CA142840