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Video-Assisted Thoracoscopic or Open Lobectomy in Early-Stage Lung Cancer.
Lim, Eric; Batchelor, Tim J P; Dunning, Joel; Shackcloth, Michael; Anikin, Vladimir; Naidu, Babu; Belcher, Elizabeth; Loubani, Mahmoud; Zamvar, Vipin; Harris, Rosie A; Dabner, Lucy; McKeon, Holly E; Paramasivan, Sangeetha; Realpe, Alba; Elliott, Daisy; De Sousa, Paulo; Stokes, Elizabeth A; Wordsworth, Sarah; Blazeby, Jane M; Rogers, Chris A.
Afiliación
  • Lim E; Academic Division of Thoracic Surgery, Royal Brompton and Harefield Hospitals, London.
  • Batchelor TJP; Imperial College London, London.
  • Dunning J; Thoracic Surgery, Bristol Royal Infirmary, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom.
  • Shackcloth M; Department of Cardiothoracic Surgery, The James Cook University Hospital, South Tees Hospitals NHS Foundation Trust, Middlesbrough, United Kingdom.
  • Anikin V; Department of Thoracic Surgery, Liverpool Heart and Chest Hospital, Liverpool, United Kingdom.
  • Naidu B; Academic Division of Thoracic Surgery, Royal Brompton and Harefield Hospitals, London.
  • Belcher E; Department of Oncology and Reconstructive Surgery, I.M. Sechenov First Moscow State Medical University, Moscow.
  • Loubani M; Department of Thoracic Surgery, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom.
  • Zamvar V; Cardiothoracic Surgery, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Harris RA; Department of Cardiothoracic Surgery, Castle Hill Hospital, Hull University Teaching Hospitals, Cottingham, United Kingdom.
  • Dabner L; Department of Cardiothoracic Surgery, Edinburgh Royal Infirmary, NHS Lothian, Edinburgh.
  • McKeon HE; Clinical Trials and Evaluation Unit, Bristol Trials Centre, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Paramasivan S; Clinical Trials and Evaluation Unit, Bristol Trials Centre, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Realpe A; Clinical Trials and Evaluation Unit, Bristol Trials Centre, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Elliott D; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • De Sousa P; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Stokes EA; National Institute for Health Research Bristol Biomedical Research Centre, Surgical Innovation Theme, Centre for Surgical Research, University of Bristol, Bristol, United Kingdom.
  • Wordsworth S; Academic Division of Thoracic Surgery, Royal Brompton and Harefield Hospitals, London.
  • Blazeby JM; Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
  • Rogers CA; National Institute for Health Research Oxford Biomedical Research Centre, Oxford, United Kingdom.
NEJM Evid ; 1(3): EVIDoa2100016, 2022 03.
Article en En | MEDLINE | ID: mdl-38319202
ABSTRACT

BACKGROUND:

There is limited randomized evidence on the comparative outcomes of early-stage lung cancer resection by video-assisted thoracoscopic surgery (VATS) versus open resection.

METHODS:

We conducted a parallel-group multicenter randomized trial that recruited participants with known or suspected early-stage lung cancer and randomly assigned them to open or VATS resection of their lesions. The primary outcome was physical function at 5 weeks as a measure of recovery using the European Organisation for Research and Treatment of Cancer core health-related quality of life questionnaire (QLQ-C30) (scores range from 0 to 100, with higher scores indicating better function; the clinical minimally important difference for improvement is 5 points). We followed the patients for an additional 47 weeks for other outcomes.

RESULTS:

A total of 503 participants were randomly assigned (247 to VATS and 256 to open lobectomy). At 5 weeks, median physical function was 73 in the VATS group and 67 in the open surgery group, with a mean difference of 4.65 points (95% confidence interval, 1.69 to 7.61). Of the participants allocated to VATS, 30.7% had serious adverse events after discharge compared with 37.8% of those allocated to open surgery (risk ratio, 0.81 [95% confidence interval, 0.66 to 1.00]). At 52 weeks, there were no differences in cancer progression-free survival (hazard ratio, 0.74 [0.43 to 1.27]) or overall survival (hazard ratio, 0.67 [0.32 to 1.40]).

CONCLUSIONS:

VATS lobectomy for lung cancer is associated with a better recovery of physical function in the 5 weeks after random assignment compared with open surgery. Long-term oncologic outcomes will require continued follow-up to assess. (Funded by the National Institute for Health Research Health Technology Assessment programme [reference number 13/04/03]; ISRCTN number, ISRCTN13472721.)
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neumonectomía / Calidad de Vida / Cirugía Torácica Asistida por Video / Neoplasias Pulmonares Tipo de estudio: Clinical_trials Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: NEJM Evid Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neumonectomía / Calidad de Vida / Cirugía Torácica Asistida por Video / Neoplasias Pulmonares Tipo de estudio: Clinical_trials Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: NEJM Evid Año: 2022 Tipo del documento: Article