A Phase II Study of T-DXd Plus SRT in HER2-positive Breast Cancer Brain Metastases

Last updated: October 14, 2023
Sponsor: Fudan University
Overall Status: Active - Not Recruiting

Phase

2

Condition

Brain Metastases

Cancer Treatment

Neoplasm Metastasis

Treatment

Combination use of SRT with T-DXd

Clinical Study ID

NCT06088056
FDRT-BC021
  • Ages > 18
  • Female

Study Summary

This research study will evaluate the efficacy and safety of stereotactic radiotherapy (SRT) combined with Trastuzumab-Deruxtecan (T-DXd; DS-8201a) in HER2-positive Breast Cancer Patients with newly diagnosed or progressing Brain Metastases.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Pathologically confirmed HER2 positive advanced breast cancer
  • Age>18 years.
  • Brain metastases confirmed by enhanced brain MRI. Metastases number less than 15.
  • KPS≥70 or KPS ≥60 with neurologic symptoms caused by BM
  • Life expectancy of more than 6 months
  • Prior therapy of oral dexamethasone not exceeding 16mg/d
  • Time interval from prior therapy was more than 2 weeks, and evaluation of adverseevents is no more than grade 1.
  • Screening laboratory values must meet the following criteria( and should be obtainedwithin 28 days prior to registration):
  1. Absolute Neutrophil Count (ANC) ≥ 1.5 x 109/L, Platelets≥ 90 x 109/L, Hemoglobin ≥ 90 g/L
  2. Aspartate aminotransferase/alanine aminotransferase (AST/ALT) ≤2.5 x ULN withoutliver metastasis,≤ 5 x ULN with liver metastases
  3. Serum BUN and creatinine ≤ 1.5 x Upper Limit of Normal (ULN)
  4. LVEF ≥ 50%
  5. QTcF < 480 ms
  6. INR≤1.5×ULN,APTT≤1.5×ULN
  • Signed the informed consent form prior to patient entry

Exclusion

Exclusion Criteria:

  • Leptomeningeal or hemorrhagic metastases
  • Uncontrolled epilepsy
  • Severe or uncontrolled disease: severe cardiovascular disease, end-stage renaldisease, severe hepatic disease, history of immunodeficiency, including HIV positive,active HBV/HCV or other acquired congenital immunodeficiency disease, or organtransplantation history, active infection, etc.
  • History of allergy to treatment regimens
  • Pregnancy or lactation period, women of child-bearing age who are unwilling to acceptcontraceptive measures.
  • Inability to complete enhanced MRI
  • Not suitable for inclusion for specific reasons judged by sponsor

Study Design

Total Participants: 17
Treatment Group(s): 1
Primary Treatment: Combination use of SRT with T-DXd
Phase: 2
Study Start date:
November 01, 2023
Estimated Completion Date:
July 31, 2026

Connect with a study center

  • Fudan University Shanghai Cancer Center

    Shanghai,
    China

    Site Not Available

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