Evidence map›Paper›PMID 31367906›Full record

Trial reportEuropean journal of nuclear medicine and molecular imaging2019

Introducing FDG PET/CT-guided chemoradiotherapy for stage III NSCLC in low- and middle-income countries: preliminary results from the IAEA PERTAIN trial.

T Konert, W V Vogel, D Paez, A Polo, E Fidarova, H Carvalho, P S Duarte, A C Zuliani, A O Santos, D Altuhhova and 17 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in European journal of nuclear medicine and molecular imaging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
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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

27 authors.

T KonertNuclear Medicine Department, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands. t.konert@nki.nl.ORCID http://orcid.org/0000-0003-4678-136X
W V VogelNuclear Medicine Department, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.
D PaezDivision of Human Health, Department of Nuclear Sciences and Applications, International Atomic Energy Agency, Vienna, Austria.
A PoloDivision of Human Health, Department of Nuclear Sciences and Applications, International Atomic Energy Agency, Vienna, Austria.
E FidarovaDivision of Human Health, Department of Nuclear Sciences and Applications, International Atomic Energy Agency, Vienna, Austria.
H CarvalhoDepartment of Radiology and Oncology, Faculty of Medicine, University of São Paulo - Institute of Cancer of Sao Paulo State, São Paulo, Brazil.
P S DuarteDepartment of Radiology and Oncology, Faculty of Medicine, University of São Paulo - Institute of Cancer of Sao Paulo State, São Paulo, Brazil.
A C ZulianiDepartment of Radiation Oncology and Nuclear Medicine Department, Hospital das Clínicas, Campinas University, Campinas, Brazil.
A O SantosDepartment of Radiation Oncology and Nuclear Medicine Department, Hospital das Clínicas, Campinas University, Campinas, Brazil.
D AltuhhovaDepartment of Radiation Oncology and Radiology Department, North Estonia Medical Center, Tallinn, Estonia.
L KarusooDepartment of Radiation Oncology and Radiology Department, North Estonia Medical Center, Tallinn, Estonia.
R KapoorDepartment of Radiation Oncology and Nuclear Medicine Department, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
A SoodDepartment of Radiation Oncology and Nuclear Medicine Department, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
J KhaderDepartment of Radiation Oncology and Nuclear Medicine Department, King Hussein Cancer Center, Amman, Jordan.
A Al-IbraheemDepartment of Radiation Oncology and Nuclear Medicine Department, King Hussein Cancer Center, Amman, Jordan.
Y NumairDepartment of Radiation Oncology and Nuclear Medicine Department, Institute of Nuclear Medicine and Oncology, Lahore, Pakistan.
S AbubakerDepartment of Radiation Oncology and Nuclear Medicine Department, Institute of Nuclear Medicine and Oncology, Lahore, Pakistan.
C SoydalDepartment of Radiation Oncology and Nuclear Medicine Department, Ankara University School of Medicine, Mamak/Ankara, Turkey.
T KütükDepartment of Radiation Oncology and Nuclear Medicine Department, Ankara University School of Medicine, Mamak/Ankara, Turkey.
T A LeDepartment of Radiation Oncology and Nuclear Medicine Department, Cho Ray Hospital, University of Ho Chi Minh City, Ho Chi Minh City, Vietnam.
N X CanhDepartment of Radiation Oncology and Nuclear Medicine Department, Cho Ray Hospital, University of Ho Chi Minh City, Ho Chi Minh City, Vietnam.
B Q BieuDepartment of Radiation Oncology and Radiosurgery, Tran Hung Dao Hospital, Hanoi, Vietnam.
L N HaDepartment of Radiation Oncology and Radiosurgery, Tran Hung Dao Hospital, Hanoi, Vietnam.
J S A BelderbosDepartment of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
M P MacManusDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
D ThorwarthSection for Biomedical Physics, Department of Radiation Oncology, University Hospital Tübingen, Tübingen, Germany.
G G HannaDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia. gerry.hanna@petermac.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatients with stage III non-small-cell lung cancer (NSCLC) treated with chemoradiotherapy (CRT) in low- and middle-income countries (LMIC) continue to have a poor prognosis. It is known that FDG PET/CT improves staging, treatment selection and target volume delineation (TVD), and although its use has grown rapidly, it is still not widely available in LMIC. CRT is often used as sequential treatment, but is known to be more effective when given concurrently. The aim of the PERTAIN study was to assess the impact of introducing FDG PET/CT-guided concurrent CRT, supported by training and quality control (QC), on the overall survival (OS) and progression-free survival (PFS) of patients with stage III NSCLC.

methodsThe study included patients with stage III NSCLC from nine medical centres in seven countries. A retrospective cohort was managed according to local practices between January 2010 and July 2014, which involved only optional diagnostic FDG PET/CT for staging (not for TVD), followed by sequential or concurrent CRT. A prospective cohort between August 2015 and October 2018 was treated according to the study protocol including FDG PET/CT in treatment position for staging and multimodal TVD followed by concurrent CRT by specialists trained in protocol-specific TVD and with TVD QC. Kaplan-Meier analysis was used to assess OS and PFS in the retrospective and prospective cohorts.

resultsGuidelines for FDG PET/CT image acquisition and TVD were developed and published. All specialists involved in the PERTAIN study received training between June 2014 and May 2016. The PET/CT scanners used received EARL accreditation. In November 2018 a planned interim analysis was performed including 230 patients in the retrospective cohort with a median follow-up of 14 months and 128 patients in the prospective cohort, of whom 69 had a follow-up of at least 1 year. Using the Kaplan-Meier method, OS was significantly longer in the prospective cohort than in the retrospective cohort (23 vs. 14 months, p = 0.012). In addition, median PFS was significantly longer in the prospective cohort than in the retrospective cohort (17 vs. 11 months, p = 0.012).

conclusionIn the PERTAIN study, the preliminary results indicate that introducing FDG PET/CT-guided concurrent CRT for patients with stage III NSCLC in LMIC resulted in a significant improvement in OS and PFS. The final study results based on complete data are expected in 2020.

Indexed as

ChemoradiotherapyPositron Emission Tomography Computed TomographyAdultAgedAged, 80 and overBrazilCarcinoma, Non-Small-Cell LungDisease-Free SurvivalEstoniaFemaleFluorodeoxyglucose F18HumansImage Processing, Computer-AssistedIndiaJordanKaplan-Meier EstimateFluorodeoxyglucose F18Low- and middle-income countriesNon-small-cell lung cancerPET/CT-guided chemoradiotherapy

Identifiers

PMID31367906
PMCPMC6717604

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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.