Clinical trial · Observational
HER-TEMPO - Real World Treatment-related Outcomes on T-DXd in Canada
Real World Study of TrEatment Discontinuations and Modifications for Patients With HER2+ and HER2-low Metastatic Breast Cancer On Trastuzumab Deruxtecan
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Trastuzumab deruxtecan (T-DXd) has been studied in multiple global prospective DESTINY-Breast trials and has a marketing authorization from Health Canada for patients with HER2-positive metastatic breast cancer (mBC) and HER2-low mBC, respectively. Multiple stakeholders, including clinicians, patients, regulators, and healthcare decision makers, are interested in real-world treatment-related outcomes in order to better represent the effectiveness of therapies in routine care settings.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| HER2-low Expressing Breast Cancer | Breast Neoplasm | PROBABILISTIC | 0.70 |
| HER2-positive Breast Cancer | HER2-Positive Breast Carcinoma | ALIAS | 0.90 |
| Metastatic Breast Cancer | Malignant Breast Neoplasm | CURATED_BROADER | 0.78 |
| Unresectable Breast Cancer | Malignant Breast Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Trastuzumab deruxtecan | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- HER2-positive
- description
- This cohort includes patients with HER2+ mBC who started treatment with T-DXd in the PSP.
- interventionNames
- Drug: Trastuzumab deruxtecan
- label
- HER2-low
- description
- This cohort includes patients with HER2-low mBC who started treatment with T-DXd in the PSP.
- interventionNames
- Drug: Trastuzumab deruxtecan
Primary outcomes (2)
- measure
- Early treatment discontinuation rates
- timeFrame
- 3, 6, 9 months
- description
- Summary statistics of cumulative number and proportion of patients discontinuing at each timepoint
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 130 Years
Show eligibility criteria text
Inclusion Criteria: Enrollment criteria for HER2-positive PSP: * Adults, 18 years of age or older * Unresectable or metastatic HER2-positive breast cancer who have received at least one prior anti-HER2-based regimen either in the metastatic setting, or in the neoadjuvant or adjuvant setting and developed disease recurrence during or within 6 months of completing neoadjuvant or adjuvant therapy * Patients must not have received a prior anti-HER2 ADC, such as trastuzumab emtansine, in the metastatic setting * Patients who received a prior anti-HER2 ADC in the adjuvant setting must have progressed \>12 months following the completion of therapy Enrollment criteria for HER2-low PSP: * Adults, 18 years of age or older * Unresectable or metastatic HER2-low (IHC 1+ or IHC 2+/ISH-) breast cancer who have received at least one prior line of chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy * Patients with HR+ breast cancer should have received at least one or be considered ineligible for endocrine therapy. Patients in the SPP must additionally meet the following criteria: * Patients must have provided consent to be contacted for future research and provided consent to participate in the current observational study Exclusion Criteria (both cohorts): * Patients who enrolled in the PSP, but did not initiate therapy with T-DXd by the end of the PSP program * Patients with medical history of Interstitial Lung Disease (ILD) / pneumonitis that required steroids or current ILD /pneumonitis * Patients who do not have adequate renal or hepatic function, defined as: * Inadequate renal function is defined as Creatinine clearance \<30 mL/min, as calculated using the Cockcroft-Gault equation . * Inadequate hepatic function is aspartate aminotransferase (AST)/alanine aminotransferase (ALT) \>5 × upper limit of normal (ULN). Total bilirubin \>1.5 × ULN if no liver metastases or ≥ 3 x ULN in the presence of documented Gilbert's syndrome (unconjugated hyperbilirubinemia) or liver metastases at baseline.
References
Publications (1)
- DERIVEDBrezden-Masley C, Qadeer R, Senhaji Mouhri Z, Salvo B, Bonar N, Spin P, Shokar S. Canadian real-world hybrid longitudinal cohort study of treatment discontinuations and modifications for patients with HER2+ and HER2-low metastatic breast cancer on trastuzumab deruxtecan enrolled in a patient support programme: the HER-TEMPO study protocol. BMJ Open. 2025 Sep 21;15(9):e100889. doi: 10.1136/bmjopen-2025-100889. PMID 40976668