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An Open-label, Multinational Study Assessing the Efficacy and Safety of Dato-DXd Treatment in Patients With HR-positive, HER2 IHC 0, Locally Advanced Inoperable or Metastatic Breast Cancer Refractory to Endocrine Therapy (TROPION-Breast06)

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521904-23-00
Acronym
D9260C00003
Enrollment
50
Registered
2025-11-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Locally Advanced Inoperable or Metastatic Breast Cancer Refractory to Endocrine Therapy

Brief summary

PFS is defined as time from date of first dose of study intervention until progression per RECIST 1.1 as assessed by the investigator or death due to any cause. The analysis will include all dosed participants. All events will be included, regardless of whether the participant withdraws from therapy, receives another anticancer therapy, or experiences clinical progression prior to RECIST 1.1.

Detailed description

Proportion of participants with oral mucositis/stomatitis . Proportion of participants with ocular events. Proportion of participants with Grade 3 or higher AEs possibly related to Dato-DXd treatment (Grade ≥ 3 treatment-related AEs) according to NCI CTCAE 5.0., CBR at 24 weeks is defined as the percentage of participants who have a confirmed CR or PR or who have SD per RECIST 1.1 as assessed by the investigator and derived from the raw tumour data for at least 24 weeks after date of first dose., ORR is defined as the proportion of participants with measurable disease at baseline who have a confirmed CR or confirmed PR, as assessed by the investigator and derived from raw tumour data per RECIST 1.1. The analysis will include all dosed participants with measurable disease at baseline., DoR will be defined as the time from the date of first documented confirmed response until date of documented progression per RECIST 1.1 as assessed by the investigator or death due to any cause. The analysis will include all dosed participants who have a confirmed response., OS defined as the time from the date of the first dose of study intervention until the date of death due to any cause. The analysis will include all dosed participants. All deaths will be included, regardless of whether the participant withdraws from therapy or receives another anticancer therapy. The measure of interest is the OS rate at 6 months.

Interventions

DRUGDatopotamab deruxtecan

Sponsors

AstraZeneca AB
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
PFS is defined as time from date of first dose of study intervention until progression per RECIST 1.1 as assessed by the investigator or death due to any cause. The analysis will include all dosed participants. All events will be included, regardless of whether the participant withdraws from therapy, receives another anticancer therapy, or experiences clinical progression prior to RECIST 1.1.

Secondary

MeasureTime frame
Proportion of participants with oral mucositis/stomatitis . Proportion of participants with ocular events. Proportion of participants with Grade 3 or higher AEs possibly related to Dato-DXd treatment (Grade ≥ 3 treatment-related AEs) according to NCI CTCAE 5.0., CBR at 24 weeks is defined as the percentage of participants who have a confirmed CR or PR or who have SD per RECIST 1.1 as assessed by the investigator and derived from the raw tumour data for at least 24 weeks after date of first dose., ORR is defined as the proportion of participants with measurable disease at baseline who have a confirmed CR or confirmed PR, as assessed by the investigator and derived from raw tumour data per RECIST 1.1. The analysis will include all dosed participants with measurable disease at baseline., DoR will be defined as the time from the date of first documented confirmed response until date of documented progression per RECIST 1.1 as assessed by the investigator or death due to any cause. The anal

Countries

France, Italy, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 19, 2026