Authorised Phase III and phase IV (Integrated) Treatment of patients with HER2-positive breast cancer with or without brain metastasis

A study to investigate the efficacy and safety of trastuzumab deruxtecan in patients With or Without Brain Metastasis Who Have Previously-Treated Advanced or Metastatic HER2 Positive Breast Cancer

EU CTIS ID: 2024-510588-53-00

What this study is testing

To describe the overall treatment effect of T DXd in HER2-positive MBC patients with or without baseline BM

  • Phase III and phase IV (Integrated)

A plain-language read of the study's public EU CTIS listing. The study team confirms the details.

Who can take part

You may be able to join if

  • Pathologically documented breast cancer that: (a) Is unresectable/advanced or metastatic, and (b) Has confirmed HER2-positive status as determined according to ASCO/CAP guidelines (Wolff et al, 2018) evaluated at a local laboratory
  • Participant must have either: (a) No evidence of BM, or (b) Untreated BM on screening contrast brain MRI / CT scan (i)not needing immediate local therapy, or (ii)For participants with untreated CNS lesions: - if lesion ≤ 2 cm, no discussion with study physician is required prior to enrollment- if lesion is > 2.0 cm, discussion with and approval from the study physician is required prior to enrollment, or (c) Previously treated stable or progressing BM (i) Previously treated BM with local therapy may either be radiographically stable for ≥ 4 weeks since completion of treatment or may have progressed since prior local CNS therapy, provided that there is no clinical indication for immediate re-treatment with local therapy (ii) Patients treated with CNS local therapy for newly identified lesions found on contrast brain MRI/CT scan performed during screening for this study who also have other sites of disease assessable by RECIST 1.1
  • Participants with BMs must be neurologically stable and: (a) Be receiving the equivalent of dexamethasone ≤ 3 mg/day if treatment is required (b) If receiving an anticonvulsant regimen, the regimen must have been stable for ≥ 14 days before first day of dosing (c) Relevant records of any CNS treatment must be available to allow for classification of TLs and NTLs
  • Previous breast cancer treatment: (a) Radiologic or objective evidence of disease progression on or after HER2 targeted therapies. Note: Disease progression within 6 months after adjuvant treatment with HER2 targeted therapies is also acceptable. (b) No more than 2 lines/regimens of therapy in the metastatic setting. Note: A line/regimen of treatment should be counted based on a progression event.

You likely can't join if

  • Known or suspected LMD
  • Prior exposure to tucatinib treatment
  • Based on screening contrast brain MRI/ CT scan, participants must not have any of the following: (a) Any untreated brain lesions > 2.0 cm in size (b) Ongoing use of systemic corticosteroids for control of symptoms of BMs at a total daily dose of > 3 mg of dexamethasone (or equivalent). (c) Any brain lesion thought to require immediate local therapy, (d) Have poorly controlled (> 1/week) generalized or complex partial seizures, or manifest neurologic progression due to BMs notwithstanding CNS-directed therapy
  • Has spinal cord compression

The study team makes the final eligibility decision.

Where it's taking place

  • Japan
  • Switzerland
  • United States
  • Canada
  • Australia
  • United Kingdom

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Japan; Switzerland; United States; Canada; Australia; United Kingdom. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.