Vegzelma (bevacizumab-adcd) vs Orserdu (elacestrant)

Vegzelma (bevacizumab-adcd) vs Orserdu (elacestrant)

Vegzelma (bevacizumab-adcd) is a biosimilar to the original bevacizumab product, which is a monoclonal antibody designed to inhibit angiogenesis by targeting vascular endothelial growth factor (VEGF), and it is commonly used in the treatment of various types of cancer, including colorectal, lung, glioblastoma, kidney, and ovarian cancers. Orserdu (elacestrant) is a selective estrogen receptor degrader (SERD) indicated for the treatment of estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer in postmenopausal women or adult men. When deciding between Vegzelma and Orserdu, the choice would largely depend on the type and characteristics of the cancer being treated; Vegzelma is used for a broader range of cancers associated with abnormal blood vessel growth, while Orserdu is specifically targeted for certain hormone receptor-positive breast cancers.

Difference between Vegzelma and Orserdu

Metric Vegzelma (bevacizumab-adcd) Orserdu (elacestrant)
Generic name Bevacizumab-adcd Elacestrant
Indications Metastatic colorectal cancer, non-small cell lung cancer, glioblastoma, metastatic renal cell carcinoma, cervical cancer, ovarian cancer, fallopian tube cancer, primary peritoneal cancer Estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer
Mechanism of action Monoclonal antibody that inhibits angiogenesis by binding to vascular endothelial growth factor (VEGF) Oral selective estrogen receptor degrader (SERD) that binds to the estrogen receptor and degrades it, inhibiting the receptor signaling in breast cancer cells
Brand names Vegzelma Orserdu
Administrative route IV infusion Oral
Side effects Hypertension, proteinuria, hemorrhage, arterial thromboembolism, gastrointestinal perforation, wound healing complications, infusion reactions Nausea, vomiting, fatigue, increased blood cholesterol, musculoskeletal pain, decreased appetite, hot flushes
Contraindications Hypersensitivity to bevacizumab or its excipients, pregnancy Hypersensitivity to elacestrant or any of its components, pregnancy, breastfeeding
Drug class Monoclonal antibody, angiogenesis inhibitor Selective estrogen receptor degrader (SERD)
Manufacturer Celltrion Healthcare Co., Ltd. Radiant Pharmaceuticals

Efficacy

Vegzelma (bevacizumab-adcd) in Gynecological Cancers

Vegzelma (bevacizumab-adcd) is a biosimilar to the original bevacizumab, a monoclonal antibody that inhibits vascular endothelial growth factor (VEGF). It is used for the treatment of various types of cancer, including gynecological cancers such as ovarian, fallopian tube, and primary peritoneal cancer. The efficacy of bevacizumab in gynecological cancers has been established through several clinical trials. It has been shown to improve progression-free survival when used in combination with chemotherapy compared to chemotherapy alone. However, it is important to note that the specific efficacy of Vegzelma, as a biosimilar, should be supported by clinical trials demonstrating its similarity to the reference product.

Orserdu (elacestrant) in Gynecological Cancers

Orserdu (elacestrant) is a selective estrogen receptor degrader (SERD) that is being investigated for the treatment of estrogen receptor-positive (ER+) breast cancer. While it is primarily focused on breast cancer, its mechanism of action suggests potential utility in other hormone-driven cancers, including gynecological cancers that express estrogen receptors. However, as of the knowledge cutoff date, the efficacy of Orserdu in gynecological cancers specifically has not been established through clinical trials. Its use in this area would be considered off-label, and further research would be necessary to confirm its efficacy for gynecological cancer patients.

Considerations for Off-Label Use

When considering off-label use of medications such as Orserdu for gynecological cancers, it is important for healthcare professionals to rely on scientific evidence, clinical judgment, and patient-specific factors. The off-label use should be supported by a thorough understanding of the drug's pharmacology, published literature, and any available data from clinical experiences. In the absence of specific data for gynecological cancers, the efficacy of Orserdu would be speculative, and healthcare providers should exercise caution and consider the risks and benefits for individual patients.

Conclusion

While Vegzelma has demonstrated efficacy in the treatment of certain gynecological cancers, Orserdu's efficacy in this area remains to be established. It is crucial for healthcare providers to stay informed about the latest clinical trials and evidence to make informed decisions regarding the use of these medications in the treatment of gynecological cancers. As with any treatment, the potential benefits must be weighed against the risks, and the use of these drugs should be guided by clinical evidence and best practices in oncology.

Regulatory Agency Approvals

Vegzelma
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Orserdu
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

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If Vegzelma 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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