Aditya Bardia, MD, MPH, FASCO, discusses how fam-trastuzumab deruxtecan-nxki compares with physician’s choice of chemotherapy in estrogen receptor-positive/HER2-low breast cancer.
Aditya Bardia, MD, MPH, FASCO, professor, department of medicine, division of hematology/oncology, director of translational research integration, UCLA Health Jonsson Comprehensive Cancer Center, Los Angeles, CA, discusses how fam-trastuzumab deruxtecan-nxki (T-DXd; Enhertu) compares with physician’s choice of chemotherapy in estrogen receptor (ER)-positive/HER2-low breast cancer and how progression speed may influence a clinicians treatment choice between the two.
Bardia then covers some of the safety outcomes observed in the DESTINY-Breast06 trial (NCT04494425) and explains what oncologists should take away from the study’s updated findings presented at the 2024 SABCS.
Transcription:
0:09 | T-DXd is a HER2-directed antibody-drug conjugate that demonstrated superiority over standard chemotherapy just after endocrine-based therapy. So, pretty much first-line therapy after endocrine-based therapy in the DESTINY-Breast06 study showed improvement in progression-free survival, and much higher response rate as well. If we look at a subgroup of patients who had rapid disease progression on first-line therapy, even in this subgroup as presented at SABCS 2024, T-DXd was superior to standard chemotherapy.
0:43 | Important [adverse] effects to remember with T-DXd, which is seen in DESTINY-Breast06, as well as other studies, include nausea, myelosuppression, but also a serious [adverse] effect is pneumonitis, grade 4. Grade 4 pneumonitis is rare, but has been seen in clinical trials. So, physicians should be aware of pneumonitis, identify pneumonitis early, and intervene early.
1:08 | T-DXd is a potential option. In ER-positive, metastatic breast cancer, whenever you are thinking of chemotherapy for a patient, that is where potentially T-DXd is an option, as seen in the DESTINY-Breast06 study.
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