
Fam-T-DXd-nxki Demonstrates Superior Outcomes in Early HER2-Positive Breast Cancer Across Phase 3 DESTINY Trials
Key Takeaways
- Fam-trastuzumab deruxtecan-nxki shows significant efficacy in high-risk early-stage HER2-positive breast cancer, improving invasive disease-free survival and pathologic complete response rates.
- The drug's mechanism involves a HER2-targeted antibody-drug conjugate, enabling effective targeting of cancer cells, including those with heterogeneous HER2 expression.
Recent trials reveal fam-trastuzumab deruxtecan-nxki's potential to transform treatment for high-risk HER2-positive breast cancer, enhancing survival rates significantly.
Recent results from two phase 3 DESTINY trials (DESTINY-Breast05; NCT04622319 and DESTINY-Breast11; NCT05113251)1,2 highlight the growing role of fam-trastuzumab deruxtecan-nxki (Enhertu; AstraZeneca, Daiichi Sankyo) as a potential practice-changing therapy for patients with high-risk early-stage breast cancer.
Breast cancer remains the most commonly diagnosed cancer among women worldwide, with human epidermal growth factor receptor 2 (HER2)-positive disease representing approximately 15% to 20% of all cases. Although advances in HER2-directed therapies have significantly improved outcomes, patients with high-risk early-stage breast cancer continue to face recurrence challenges despite standard-of-care treatment. These two recent trials show promising results for patients and could represent a new standard of care for some patients with breast cancer.
DESTINY-Breast05: Fam-Trastuzumab Deruxtecan-nxki vs T-DM1 in the Adjuvant Setting
The DESTINY-Breast05 trial compared fam-trastuzumab deruxtecan-nxki to ado-trastuzumab emtansine (T-DM1) in patients with high-risk, HER2-positive early breast cancer who had residual invasive disease after neoadjuvant therapy. The results showed a statistically significant and clinically very important prolongation of invasive disease-free survival (iDFS) when fam-trastuzumab deruxtecin-nxki was used versus T-DM1. This finding led to the first antibody-drug conjugate (ADC) to show superiority in this head-to-head setting.1,3
DESTINY-Breast11: Fam-Trastuzumab Deruxtecan-nxki in the Neoadjuvant Setting
The DESTINY-Breast11 trial was simultaneously conducted to compare fam-trastuzumab deruxtecan-nxki followed by a trastuzumab/pertuzumab-based chemotherapy regimen (THP) with standard-of-care therapies in the neoadjuvant setting for patients with high-risk, HER2-positive early-stage disease. The outcomes showed that improvement in pathologic complete response (pCR) rates with the fam-trastuzumab deruxtecan-nxki–based regimen was statistically significant and clinically meaningful.2,4
Neoadjuvant therapy leading to pCR has been correlated to reduced disease recurrence and survival extension. By significantly improving pCR rates, fam-trastuzumab deruxtecan-nxki could reshape the treatment paradigm for HER2-positive breast cancer patients at risk of recurrence after surgery.
Clinical Context and Mechanism of Action
Fam-trastuzumab deruxtecan-nxki is a HER2-targeted antibody-drug conjugate that connects trastuzumab to a topoisomerase I inhibitor payload through a cleavable linker. The treatment has shown strong activity in several cancers, notably heavily pretreated HER2-positive metastatic breast cancer, HER2-low breast cancer, gastric cancer, and non-small cell lung cancer.5
The structure of the ADC makes it possible for the 'bystander effect,' which means that the toxic payload can still reach the surrounding cancer cells that are not depending on the heterogeneity of HER2 expression. Such a process is especially important in the early stage of the disease when small metastatic or leftover cells with different HER2 expression might be present.
Implications for Pharmacists and Patient Care
One of the main roles of pharmacists in the process of fam-trastuzumab deruxtecan-nxki integration into practice will be to explain to patients the advantages and risks of ADC therapy in comparison with the previously used treatments. Besides that, they will be safety supervisors, especially for the occurrence of interstitial lung disease (ILD)—a side effect that may develop due to the use of fam-trastuzumab deruxtecan-nxki and thus requires prevention through immediate diagnosis and treatment of the case. In addition, pharmacists can help optimize adherence and coordinate multidisciplinary care to ensure patients receive guideline-directed treatment sequencing and the best possible outcomes.
What Does This Mean for Patients and Pharmacists?
The phase 3 DESTINY-Breast05 and DESTINY-Breast11 trials have verified that fam-trastuzumab deruxtecan-nxki offers notable clinical benefits beyond the currently available standards in both the adjuvant and neoadjuvant settings for high-risk HER2-positive early breast cancer. The findings of these studies deepen the indications of the drug in advanced breast cancer and have the potential to change the way breast cancer at an earlier stage is treated.
Pharmacists will be an essential part of the process, as they will be responsible for integrating fam-trastuzumab deruxtecan-nxki into practice, patient counseling, safety monitoring, and thus facilitating the achievement of long-term positive outcomes.
REFERENCES
A Study of Trastuzumab Deruxtecan (T-DXd) Versus Trastuzumab Emtansine (T-DM1) in High-risk HER2-positive Participants With Residual Invasive Breast Cancer Following Neoadjuvant Therapy (DESTINY-Breast05). Clinicaltrials.gov. Published May9, 2025. Accessed September 20, 2025.
https://clinicaltrials.gov/study/NCT04622319 Trastuzumab Deruxtecan (T-DXd) Alone or in Sequence With THP, Versus Standard Treatment (ddAC-THP), in HER2-positive Early Breast Cancer. Clinicaltrials.gov. Published August 8, 2025. Accessed September 30, 2025.
https://clinicaltrials.gov/study/NCT05113251 ENHERTU® (fam-trastuzumab deruxtecan-nxki) demonstrated highly statistically significant and clinically meaningful improvement in invasive disease-free survival vs. T-DM1 in DESTINY-Breast05 Phase III trial in patients with high-risk early breast cancer following neoadjuvant therapy. Published September 29, 2025.
https://www.astrazeneca-us.com/media/press-releases/2025/ENHERTU-fam-trastuzumab-deruxtecan-nxki-demonstrated-highly-statistically-significant-and-clinically-meaningful-improvement-in-invasive-disease-free-survival-vs-T-DM1-in-DESTINY-Breast05-Phase-III-trial-in-patients-with-high-risk-early-breast-cancer-following-neoadjuvant-therapy.html ENHERTU® (fam-trastuzumab deruxtecan-nxki) followed by THP before surgery showed statistically significant and clinically meaningful improvement in pathologic complete response in patients with high-risk HER2-positive early-stage breast cancer in DESTINY-Breast11 Phase III trial. Astrazeneca-us.com. May 7, 2025. Accessed September 30, 2025.
https://www.astrazeneca-us.com/media/press-releases/2025/ENHERTU-fam-trastuzumab-deruxtecan-nxki-followed-by-THP-before-surgery-showed-statistically-significant-and-clinically-meaningful-improvement-in-pathologic-complete-response-in-patients-with-high-risk-HER2-positive-early-stage-breast-cancer-in-DESTINY-Breast11-Phase-III-trial.html Modi S, Jacot W, Yamashita T, et al. Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer. New England Journal of Medicine. 2022;387(1). doi:10.1056/nejmoa2203690
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