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Management of solitary fibrous tumours of the pleura: a systematic review and meta-analysis.
Mercer, Rachel M; Wigston, Charlotte; Banka, Radhika; Cardillo, Giuseppe; Benamore, Rachel; Nicholson, Andrew G; Asciak, Rachelle; Hassan, Maged; Hallifax, Robert J; Wing, Louise; Bedawi, Eihab O; Maskell, Nick A; Harriss, Elinor K; Miller, Robert F; Rahman, Najib M.
Afiliação
  • Mercer RM; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
  • Wigston C; Oxford Centre for Respiratory Medicine, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Banka R; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
  • Cardillo G; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
  • Benamore R; San Camillo Forlanini Hospital, Rome, Italy.
  • Nicholson AG; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
  • Asciak R; Dept of Histopathology, Royal Brompton and Harefield NHS Foundation Trust, and National Heart and Lung Institute, Imperial College, London, UK.
  • Hassan M; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
  • Hallifax RJ; Oxford Centre for Respiratory Medicine, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Wing L; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
  • Bedawi EO; Oxford Centre for Respiratory Medicine, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Maskell NA; Chest Diseases Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
  • Harriss EK; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
  • Miller RF; Oxford Centre for Respiratory Medicine, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Rahman NM; University of Oxford Respiratory Trials Unit, Churchill Hospital, Oxford, UK.
ERJ Open Res ; 6(3)2020 Jul.
Article em En | MEDLINE | ID: mdl-32832532
BACKGROUND: Solitary fibrous tumours of the pleura (SFTP), or pleural fibromas, are rare tumours that generally, but not universally, follow a benign course. Surgical resection is the standard treatment, but there are no evidence-based guidelines regarding the management of these tumours. METHODS: Five databases were searched from inception to April 1, 2019 for studies reporting on SFTP management. RESULTS: Twenty-seven studies met the inclusion criteria (1542 patients, all non-comparative case series); 98% of these patients underwent resection and all SFTP included were pathologically diagnosed. 394 out of 1299 cases (30.5%, 95% CI 27.8-32.8%) were malignant with recurrence rates of between 0% and 42.9%. A pleural effusion was always associated with a negative outcome, but no other features were consistently reported to have negative associations. Preoperative biopsies incorrectly reported malignant histology in two studies. Over 25% of cases of recurrence occurred when a complete (R0) resection had been achieved. The first recurrence occurred >5 years after the initial resection in at least 23% of cases. CONCLUSIONS: There is strong evidence to support long-term surveillance after surgical resection of SFTP, even where a complete (R0) resection has been achieved; however, there is no clear evidence to inform clinicians regarding the selection of patients who should undergo resection. The rates of malignant SFTP and SFTP recurrence are higher than previously reported. Only those that were pathologically diagnosed or resected were included, which may bias the data towards more aggressive tumours. Data collection on radiologically diagnosed SFTP is required to draw conclusions regarding the timing and need for intervention.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article