Study Protocol of SURVIVE HERoes (NCT06643585): Trastuzumab Deruxtecan for molecular relapse in HER2+/ Low early breast cancer with ctDNA positivity after primary therapy

TL;DR

This study tests if trastuzumab deruxtecan can clear ctDNA in early breast cancer patients with molecular relapse, potentially offering a new treatment approach.

Contribution

The trial introduces a novel approach of treating ctDNA-positive patients without visible recurrence using an antibody-drug conjugate.

Findings

The trial aims to evaluate ctDNA clearance after 12 months of treatment with trastuzumab deruxtecan.

It may redefine breast cancer staging and treatment by targeting molecular residual disease.

180 patients will be enrolled and randomized in a 2:1 ratio for the study.

Abstract

Current evidence on circulating tumor DNA (ctDNA) in the adjuvant setting of early breast cancer (eBC) confirms its high prognostic value. CtDNA-positive patients without radiographic signs of relapse show reduced disease-free and overall survival. Secondary adjuvant treatment intervention studies represent a new appealing therapeutic option.

We present SURVIVE HERoes, a phase III randomized clinical trial of the potent antibody-drug conjugate trastuzumab deruxtecan versus standard of care (SoC) in patients with HER2 positive or HER2 low eBC and molecular residual or recurrent disease (ctDNA positive, cM0) after primary therapy. The primary endpoint is the ctDNA clearance rate after 12 months of therapeutic intervention. A total of 180 study participants will be enrolled and randomized in a 2:1 ratio to receive trastuzumab deruxtecan or SoC therapy. The trial is accompanied by an extensive translational research project.

Treating ctDNA positive patients without radiographic signs of recurrence is a novel approach. If SURVIVE HERoes and similar studies targeting MRD will be positive, this may lead the way to a new molecular understanding of breast cancer stages and individualized therapy and may open a new therapeutic window for cure.

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