Predicting the Risk of Disease Recurrence and Death Following Curative-intent Radiotherapy for Non-small Cell Lung Cancer: The Development and Validation of Two Scoring Systems From a Large Multicentre UK Cohort.


Journal

Clinical oncology (Royal College of Radiologists (Great Britain))
ISSN: 1433-2981
Titre abrégé: Clin Oncol (R Coll Radiol)
Pays: England
ID NLM: 9002902

Informations de publication

Date de publication:
03 2021
Historique:
received: 14 04 2020
revised: 30 07 2020
accepted: 02 09 2020
pubmed: 27 9 2020
medline: 15 10 2021
entrez: 26 9 2020
Statut: ppublish

Résumé

There is a paucity of evidence on which to produce recommendations on neither the clinical nor the imaging follow-up of lung cancer patients after curative-intent radiotherapy. In the 2019 National Institute for Health and Care Excellence lung cancer guidelines, further research into risk-stratification models to inform follow-up protocols was recommended. A retrospective study of consecutive patients undergoing curative-intent radiotherapy for non-small cell lung cancer from 1 October 2014 to 1 October 2016 across nine UK trusts was carried out. Twenty-two demographic, clinical and treatment-related variables were collected and multivariable logistic regression was used to develop and validate two risk-stratification models to determine the risk of disease recurrence and death. In total, 898 patients were included in the study. The mean age was 72 years, 63% (562/898) had a good performance status (0-1) and 43% (388/898), 15% (134/898) and 42% (376/898) were clinical stage I, II and III, respectively. Thirty-six per cent (322/898) suffered disease recurrence and 41% (369/898) died in the first 2 years after radiotherapy. The ASSENT score (age, performance status, smoking status, staging endobronchial ultrasound, N-stage, T-stage) was developed, which stratifies the risk for disease recurrence within 2 years, with an area under the receiver operating characteristic curve (AUROC) for the total score of 0.712 (0.671-0.753) and 0.72 (0.65-0.789) in the derivation and validation sets, respectively. The STEPS score (sex, performance status, staging endobronchial ultrasound, T-stage, N-stage) was developed, which stratifies the risk of death within 2 years, with an AUROC for the total score of 0.625 (0.581-0.669) and 0.607 (0.53-0.684) in the derivation and validation sets, respectively. These validated risk-stratification models could be used to inform follow-up protocols after curative-intent radiotherapy for lung cancer. The modest performance highlights the need for more advanced risk prediction tools.

Identifiants

pubmed: 32978027
pii: S0936-6555(20)30362-9
doi: 10.1016/j.clon.2020.09.001
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

145-154

Informations de copyright

Copyright © 2020 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.

Auteurs

M Evison (M)

Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK. Electronic address: m.evison@nhs.net.

E Barrett (E)

Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK.

A Cheng (A)

Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK.

A Mulla (A)

Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK.

G Walls (G)

Northern Ireland Cancer Centre, Belfast, UK.

D Johnston (D)

Cancer Centre Belfast City Hospital, Belfast, UK.

J McAleese (J)

Cancer Centre Belfast City Hospital, Belfast, UK.

K Moore (K)

NHS Greater Glasgow & Clyde, Glasgow, UK.

J Hicks (J)

NHS Greater Glasgow & Clyde, Glasgow, UK.

K Blyth (K)

NHS Greater Glasgow & Clyde, Glasgow, UK.

M Denholm (M)

Cambridge University Hospitals NHS Trust, Cambridge, UK.

L Magee (L)

Cambridge University Hospitals NHS Trust, Cambridge, UK.

D Gilligan (D)

Cambridge University Hospitals NHS Trust, Cambridge, UK.

S Silverman (S)

University College London Hospital, London, UK.

C Hiley (C)

CRUK Lung Cancer Centre of Excellence, UCL Cancer Institute, London, UK.

M Qureshi (M)

Weston Park Hospital, Sheffield, UK.

H Clinch (H)

The University of Sheffield Medical School, Sheffield, UK.

M Hatton (M)

Weston Park Hospital, Sheffield, UK.

L Philipps (L)

Royal Marsden Hospital, London, UK.

S Brown (S)

The Christie NHS Foundation Trust, Manchester, UK.

M O'Brien (M)

Royal Marsden Hospital, London, UK.

F McDonald (F)

Royal Marsden Hospital, London, UK.

C Faivre-Finn (C)

The Christie NHS Foundation Trust, Manchester, UK; The University of Manchester, Manchester, UK.

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Classifications MeSH