DESTINY-PANTUMOUR04

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-130
SponsorAstraZeneca

About this trial

This study will evaluate the effectiveness of T-DXd in patients with HER2-positive (IHC 3+) locally advanced, unresectable, or metastatic solid tumors who have received prior systemic treatment for metastatic or advanced disease and have no satisfactory alternative treatment options in a real-world setting in the US

Eligibility criteria

Qualifiers

Adults aged ≥18 years

Patients with locally advanced, unresectable, or metastatic HER2-positive (IHC 3+) solid tumors who have received prior systemic treatment for metastatic or advanced disease and have no satisfactory alternative treatment options as determined by the Investigator (see Exclusion Criterion 1 for excluded solid tumors);

A clinician decision has been made for treatment with T-DXd in accordance with the FDA label;

HER2-positive (IHC 3+) by local testing prior to study enrolment at the time of signed and dated informed consent;

Disqualifiers

Primary diagnosis of adenocarcinoma of the breast, adenocarcinoma of the colon or rectum, NSCLC, adenocarcinoma of the gastric body or gastroesophageal junction or hematological malignancies;

Prior T-DXd therapy;

Patients without a baseline assessment of tumor burden undertaken prior to initiating T-DXd.

Patient is participating in a clinical trial at time of enrolment

Trial design

Treatments tested in this trial

  • Trastuzumab deruxtecan

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators