Evidence map›Paper›PMID 35387421›Full record

ArticleAdvances in radiation oncology

Prognostic Value of Early Fluorodeoxyglucose-Positron Emission Tomography Response Imaging and Peripheral Immunologic Biomarkers: Substudy of a Phase II Trial of Risk-Adaptive Chemoradiation for Unresectable Non-Small Cell Lung Cancer.

Stephen R Bowen, Daniel S Hippe, Hannah M Thomas, Balukrishna Sasidharan, Paul D Lampe, Christina S Baik, Keith D Eaton, Sylvia Lee, Renato G Martins, Rafael Santana-Davila and 7 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Advances in radiation oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02773238 (Personalized Radiation Therapy Through Functional Lung Avoidance and Response-Adaptive Dose Escalation), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 34% 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.

NCT02773238 phase2completednot on this map

Personalized Radiation Therapy Through Functional Lung Avoidance and Response-Adaptive Dose Escalation: Utilizing Multimodal Molecular Imaging to Improve the Therapeutic Ratio (FLARE RT)

TypeinterventionalSponsorUniversity of WashingtonRan2016 to 2023Enrolled51ConditionsStage IIB Lung Non-Small Cell Carcinoma AJCC v7, Stage IIIA Lung Non-Small Cell Cancer AJCC v7, Stage IIIB Lung Non-Small Cell Cancer AJCC v7ArmsComputed Tomography, Fludeoxyglucose F-18, Laboratory Biomarker Analysis, Positron Emission Tomography, Radiation Therapy
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 3 citations in OpenAlex.

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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

17 authors at 5 institutions in 2 countries.

Stephen R BowenRadiation Oncology and.
Daniel S HippeRadiology, University of Washington School of Medicine, Seattle, Washington.
Hannah M ThomasDepartment of Radiation Oncology, Christian Medical College, Vellore, India.
Balukrishna SasidharanDepartment of Radiation Oncology, Christian Medical College, Vellore, India.
Paul D LampeHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Christina S BaikDivision of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Keith D EatonDivision of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Sylvia LeeDivision of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Renato G MartinsDivision of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Rafael Santana-DavilaDivision of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Delphine L ChenRadiology, University of Washington School of Medicine, Seattle, Washington.
Paul E KinahanRadiology, University of Washington School of Medicine, Seattle, Washington.
Robert S MiyaokaRadiology, University of Washington School of Medicine, Seattle, Washington.
Hubert J VesselleRadiology, University of Washington School of Medicine, Seattle, Washington.
A McGarry HoughtonHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Ramesh RenganRadiation Oncology and.
Jing ZengRadiation Oncology and.
University of Washington · USUniversity of Washington Medical Center · USFred Hutch Cancer Center · USChristian Medical College, Vellore · INRadiation Oncology Associates · US

Funding

Project 4: Risk stratification for pulmonary nodules detected by CT imaging using plasma and imaging biomarkersP50CA228944 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI A McGarry Houghton · 2019 to 2026
$19.6M
Biomarkers of Response to Immuno-chemotherapy & oliGometastatic Hypofractionated radioTherapy (BRIGHT) for Lung Cancer: Synergy of PET/CT Imaging and Peripheral Blood AssaysR01CA258997 · NCI · UNIVERSITY OF WASHINGTON · PI Stephen R. Bowen, Jing Zeng · 2022 to 2026
$2.8M
Personalized radiation therapy through functional lung avoidance and response-adaptive dose escalation: utilizing multimodal molecular imaging to improve the therapeutic ratioR01CA204301 · NCI · UNIVERSITY OF WASHINGTON · PI BOWEN, STEPHEN R., ZENG, JING · 2016 to 2020
$2.3M
NCI NIH HHS P50 CA228944NCI NIH HHS R01 CA204301NCI NIH HHS R01 CA258997
6 · The paper itself

Abstract

Purpose: We sought to examine the prognostic value of fluorodeoxyglucose-positron emission tomography (PET) imaging during chemoradiation for unresectable non-small cell lung cancer for survival and hypothesized that tumor PET response is correlated with peripheral T-cell function. Methods and Materials: Forty-five patients with American Joint Committee on Cancer version 7 stage IIB-IIIB non-small cell lung cancer enrolled in a phase II trial and received platinum-doublet chemotherapy concurrent with 6 weeks of radiation (NCT02773238). Fluorodeoxyglucose-PET was performed before treatment start and after 24 Gy of radiation (week 3). PET response status was prospectively defined by multifactorial radiologic interpretation. PET responders received 60 Gy in 30 fractions, while nonresponders received concomitant boosts to 74 Gy in 30 fractions. Peripheral blood was drawn synchronously with PET imaging, from which germline DNA sequencing, T-cell receptor sequencing, and plasma cytokine analysis were performed. Results: Median follow-up was 18.8 months, 1-year overall survival (OS) 82%, 1-year progression-free survival 53%, and 1-year locoregional control 88%. Higher midtreatment PET total lesion glycolysis was detrimental to OS (1 year 87% vs 63%, Conclusions: Midchemoradiation PET imaging is prognostic for survival; PET response may be linked to tumor and peripheral T-cell biomarkers.

Identifiers

PMID35387421
PMCPMC8977846
OpenAlexW3217080958

What OpenQuestion holds

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Registered trials

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.