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Multidisciplinary management of phyllodes tumours and breast sarcoma: a cross-sectional survey of clinical practice across the United Kingdom and Ireland

  • Mai K. Bishr*
  • , Jenny Banks
  • , Mohamed S. Abdelaziz
  • , Marwa Badawi
  • , Peter W. Crane
  • , Urszula Joanna Donigiewicz
  • , Mohamed Elkorety
  • , Mina Girgis
  • , Alex Humphreys
  • , Jen Isherwood
  • , Jennifer Kahan
  • , Stephen Keelan
  • , Ebba K. Lindqvist
  • , Ioanna Nixon
  • , Helena Sackey
  • , Carl Sars
  • , Hesham Soliman
  • , Nader Touqan
  • , Dionysios Dennis Remoundos
  • , Mahbubl Ahmed
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Aims: Phyllodes tumours and breast sarcomas are uncommon tumours and their rarity poses significant challenges in diagnosis and management. This cross-sectional study was conducted to evaluate the multidisciplinary clinical practice for these tumours across the UK and Ireland, with the aim of identifying gaps in knowledge and providing direction for establishing national guidelines.

Materials and methods: An international survey was adapted and circulated to breast and/or sarcoma surgeons and oncologists in the UK and Ireland through national organisations. Multidisciplinary team (MDT) responses were analysed anonymously.

Results: Twenty-eight MDTs participated in this study, predominately from high-volume units (85.5%). Although only 43% of the surveyed units were part of a trust that holds a sarcoma MDT, 68% of units managed malignant phyllodes and angiosarcoma, whereas 64.5% managed soft-tissue sarcoma of the breast. Across all subtypes, axillary surgery was recommended by 14–21% of the MDTs and the most recommended resection margins for breast surgery were ‘no tumour on ink’ in benign phyllodes (39%) and 10 mm in the remaining subtypes (25–29%). Immediate breast reconstruction was supported by 11–18% of MDTs for breast sarcoma subtypes, whereas 36% and 32% advocated this approach in benign and borderline phyllodes tumours, respectively. Adjuvant radiotherapy and chemotherapy were recommended by up to 29% and 11% of the MDTs, respectively.

Conclusion: The results of this study demonstrate a wide variation in clinical practice across the surveyed MDTs. As only 28 MDTs participated in our study, with under-representation from low-volume units, our results might be an underestimation of the variability in practice across the UK and Ireland. This multi-institutional study sheds light on controversial aspects in the management of phyllodes tumours and breast sarcoma, identifies the need for national guidelines to inform best practice, and calls for the centralisation of the management of breast sarcoma within specialist centres.
Original languageEnglish
Pages (from-to)e31-e39
Number of pages19
JournalClinical Oncology
Volume36
Issue number1
Early online date21 Oct 2023
DOIs
Publication statusPublished - 31 Jan 2024

Funding

Mai K. Bishr ( NIHR Academic Clinical Fellowship award, Institute of Cancer Research UK, ACF-2022-22-002) is funded by Health Education England (HEE)/ NIHR for this research project. The views expressed in this publication are those of the author(s) and not necessarily those of the NIHR, Institute of Cancer Research UK, NHS or the UK Department of Health and Social Care. The funding source had no involvement in any aspect of this study design, data collection, analysis or interpretation. Figures were created with BioRender. In non-radiation-induced breast angiosarcoma, also known as primary breast angiosarcoma, there is evidence from retrospective studies and meta-analysis that adjuvant radiotherapy improves local control, but not survival outcomes [35–37]. Similar local control outcomes were reported for STS of the breast [38,39], with evidence supporting improved survival with adjuvant radiotherapy for tumours >5 cm [40]. Among the participating MDTs in this study, up to 25% recommended adjuvant radiotherapy for angiosarcoma and up to 29% for STS.Mai K. Bishr (NIHR Academic Clinical Fellowship award, Institute of Cancer Research UK, ACF-2022-22-002) is funded by Health Education England (HEE)/NIHR for this research project. The views expressed in this publication are those of the author(s) and not necessarily those of the NIHR, Institute of Cancer Research UK, NHS or the UK Department of Health and Social Care. The funding source had no involvement in any aspect of this study design, data collection, analysis or interpretation. Figures were created with BioRender.

Keywords

  • angiosarcoma
  • breast sarcoma
  • management
  • phyllodes
  • radiotherapy
  • surgical margin

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