Enhertu (fam-trastuzumab deruxtecan-nxki) vs Orserdu (elacestrant)

Enhertu (fam-trastuzumab deruxtecan-nxki) vs Orserdu (elacestrant)

Enhertu (fam-trastuzumab deruxtecan-nxki) is an antibody-drug conjugate specifically designed for the treatment of HER2-positive breast cancer, targeting the HER2 protein and delivering chemotherapy directly to the cancer cells. Orserdu (elacestrant), on the other hand, is a selective estrogen receptor degrader (SERD) indicated for the treatment of estrogen receptor-positive (ER+) breast cancer, which works by binding to the estrogen receptor and degrading it, thus inhibiting the growth of cancer cells. When deciding between Enhertu and Orserdu, it is crucial to consider the specific type of breast cancer involved, as the effectiveness of each medication is dependent on the cancer's receptor status (HER2-positive for Enhertu and ER-positive for Orserdu), and to consult with a healthcare provider for a personalized treatment plan.

Difference between Enhertu and Orserdu

Metric Enhertu (fam-trastuzumab deruxtecan-nxki) Orserdu (elacestrant)
Generic name Fam-trastuzumab deruxtecan-nxki Elacestrant
Indications HER2-positive breast cancer ER+/HER2- advanced or metastatic breast cancer
Mechanism of action HER2-directed antibody and topoisomerase inhibitor conjugate Estrogen receptor antagonist
Brand names Enhertu Orserdu
Administrative route Injection Oral
Side effects Nausea, fatigue, vomiting, alopecia, constipation, decreased appetite, anemia, neutropenia, diarrhea, leukopenia, cough, and thrombocytopenia Hot flush, nausea, fatigue, musculoskeletal pain, and vomiting
Contraindications History of interstitial lung disease or pneumonitis Not specified
Drug class Antibody-drug conjugate Selective estrogen receptor degrader (SERD)
Manufacturer Daiichi Sankyo and AstraZeneca Radiant Pharmaceuticals

Efficacy

Enhertu (fam-trastuzumab deruxtecan-nxki) for Breast Cancer

Enhertu, also known by its generic name fam-trastuzumab deruxtecan-nxki, is a targeted therapy used for the treatment of breast cancer. Specifically, it is indicated for adult patients with unresectable or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2-based regimens in the metastatic setting. The efficacy of Enhertu was demonstrated in a pivotal phase II trial, where it showed a significant improvement in objective response rate (ORR) and progression-free survival (PFS) compared to other treatments. Patients treated with Enhertu experienced a higher rate of response to therapy, indicating a reduction in tumor size, and a longer duration before the disease progressed, which underscores its efficacy in this patient population.

Orserdu (elacestrant) for Breast Cancer

Orserdu, with the generic name elacestrant, is a selective estrogen receptor degrader (SERD) that has shown promise in the treatment of estrogen receptor-positive (ER+), HER2-negative advanced or metastatic breast cancer. Orserdu is particularly evaluated for patients who have received prior endocrine therapy. Clinical trials assessing the efficacy of Orserdu have indicated that it can provide a clinical benefit in terms of PFS in this subset of breast cancer patients. The drug's efficacy is highlighted by its ability to target and degrade the estrogen receptor, thereby inhibiting the growth of cancer cells that rely on this pathway.

Comparative Efficacy in Breast Cancer Treatment

When comparing Enhertu and Orserdu, it is essential to consider that they target different subtypes of breast cancer and mechanisms of action. Enhertu is focused on HER2-positive cases and acts as an antibody-drug conjugate, delivering cytotoxic agents directly to cancer cells. In contrast, Orserdu is used for ER+, HER2-negative breast cancer and functions by disrupting the estrogen receptor signaling pathway. Both medications have shown efficacy in their respective indications and represent significant advancements in the personalized treatment of breast cancer. The choice between these therapies would depend on the specific molecular characteristics of the breast cancer being treated.

Conclusion

Both Enhertu and Orserdu have made substantial contributions to the treatment landscape of breast cancer, offering new hope for patients with specific subtypes of the disease. The efficacy of Enhertu in HER2-positive breast cancer and Orserdu in ER+, HER2-negative breast cancer has been supported by clinical trials, which demonstrate their roles in improving patient outcomes. As research continues, these medicines may further establish themselves as key components of breast cancer therapy, potentially improving survival rates and quality of life for many patients.

Regulatory Agency Approvals

Enhertu
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Orserdu
  • Food and Drug Administration (FDA), USA

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If Enhertu or Orserdu are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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