Spatial Location of Breast Cancer Local Recurrence After Mastectomy

NCT06130111 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 170

Last updated 2023-11-14

No results posted yet for this study

Summary

Rationale:To improve the definition of the target volume for radiotherapy of the chestwall after different types of mastectomy, the exact localization of regions at risk for a local recurrence should be known. However, there are currently insufficient data in literature showing where local recurrences occur after different types of mastectomy.

Objective: The primary objective of the proposed study is to determine whether the spatial, location of a breast cancer recurrence after mastectomy, differs for different types of mastectomy.

Study design: Retrospective study evaluating spatial location and site of recurrences after mastectomy.

Study population: The investigators aim to include all breast cancer patients treated with mastectomy in the Netherlands between 2003- 2008, and known to have experienced a local recurrence as the first site of failure.

Primary endpoint: Spatial location of local recurrence (e.g., primary tumour bed, scar, skin, subcutaneous, nipple, areola, pectoral muscles).

Conditions

Interventions

PROCEDURE

Mastectomy

Mastectomy as a surgical procedure for breast cancer (regardless of perioperative treatment).

Sponsors & Collaborators

  • Albert Schweitzer Hospital

    collaborator OTHER
  • Canisius-Wilhelmina Hospital

    collaborator OTHER
  • Diakonessenhuis, Utrecht

    collaborator OTHER
  • Erasmus Medical Center

    collaborator OTHER
  • Franciscus Gasthuis

    collaborator OTHER
  • Haaglanden Medical Centre

    collaborator OTHER
  • Jeroen Bosch Ziekenhuis

    collaborator OTHER
  • Maastricht University Medical Center

    collaborator OTHER
  • Maxima Medical Center

    collaborator OTHER
  • St. Antonius Hospital

    collaborator OTHER
  • Laurentius ziekenhuis

    collaborator UNKNOWN
  • VieCuri Medical Centre

    collaborator OTHER
  • NKI-AvL

    collaborator UNKNOWN
  • Ziekenhuis Netwerk Antwerpen (ZNA)

    collaborator OTHER
  • Aarhus University Hospital

    collaborator OTHER
  • Sheba Medical Center

    collaborator OTHER_GOV
  • University of Florence

    collaborator OTHER
  • Maastricht Radiation Oncology

    lead OTHER

Principal Investigators

  • Liesbeth Boersma, Prof. · Maastro

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2023-12-01
Completion
2024-01-01

Countries

  • Netherlands

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06130111 on ClinicalTrials.gov