NEPA in Patients With HER2-positive or HER2-low Advanced Breast Cancer Treated With T-DXd

Prior treatment

• Patients who experienced nausea and/or vomiting within 7 days prior to the first cycle of T-DXd treatment
• Patients requiring treatment with steroids, antiemetics, benzodiazepines, antipsychotics, or other contraindicated drugs, including but not limited to pimozide, terfenadine, astemizole, cisapride, rifampin, carbamazepine, phenytoin, ketoconazole, itraconazole, nefazodone, troleandomycin, clarithromycin, fluvoxamine, SSRIs, SNRIs, ritonavir, or nelfinavir.

Other illness

• Patients with hypersensitivity to any components of the drug or 5-HT3 receptor antagonists.
• Any illness or condition that, in the opinion of the Investigator, may pose unwarranted risks in administering T-DXd or NEPA to the patient.

Other

• Leptomeningeal metastasis and/or brain metastasis
• Pregnant women or those suspected of being pregnant, as well as breastfeeding mothers.

• Age \>19 years
• Histologically confirmed breast cancer with metastatic or locally advanced breast cancer not amenable to definitive surgery, with or without measurable disease
• Stage IV breast cancer at initial diagnosis (de novo) or progression at distant metastatic sites following curative surgery
• HER2-positive breast cancer (HER2 IHC 3+ or IHC 2+/ISH-positive) or HER2-low breast cancer (HER2 IHC 2+/ISH-negative or HER2 IHC 1+), as defined by the ASCO/CAP guidelines
• ECOG performance status 0-2
• Patients who are scheduled to initiate their first cycle of T-DXd therapy
• Patients who are scheduled to receive netupitant/palonosetron (NEPA) for the prevention of acute and delayed CINV according to the approved indications and dosage instructions
• Patients who agree to use highly effective contraception methods or not of childbearing potential. Highly effective contraception methods include:
  • Total abstinence (when this is in line with the preferred and usual lifestyle of the subject). Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception.
  • Total hysterectomy (surgical removal of the uterus and cervix) or tubal ligation (getting your "tubes tied") at least six weeks before taking study treatment.
  • Male sterilization (at least 6 months prior to screening). For female subjects on the study, the vasectomized male partner should be the sole partner for that subject.
  • Combination of the following:
  • Placement of an intrauterine device (IUD) or intrauterine system (IUS) II. Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository
• Written informed consent