Kadcyla (trastuzumab emtansine) vs Trodelvy (sacituzumab govitecan-hziy)

Kadcyla (trastuzumab emtansine) vs Trodelvy (sacituzumab govitecan-hziy)

Kadcyla (trastuzumab emtansine) is a targeted therapy specifically designed for HER2-positive breast cancer, combining the HER2-targeting properties of trastuzumab with the chemotherapy agent emtansine. Trodelvy (sacituzumab govitecan-hziy), on the other hand, is an antibody-drug conjugate that targets the Trop-2 antigen and is used for the treatment of triple-negative breast cancer, a different subtype of breast cancer that does not express HER2, estrogen, or progesterone receptors. The choice between Kadcyla and Trodelvy would largely depend on the specific breast cancer subtype and biomarker status of the individual, as well as the overall treatment plan determined by the healthcare provider.

Difference between Kadcyla and Trodelvy

Metric Kadcyla (trastuzumab emtansine) Trodelvy (sacituzumab govitecan-hziy)
Generic name Trastuzumab emtansine Sacituzumab govitecan-hziy
Indications HER2-positive breast cancer Triple-negative breast cancer, urothelial cancer
Mechanism of action HER2 targeting antibody-drug conjugate Antibody-drug conjugate targeting TROP-2
Brand names Kadcyla Trodelvy
Administrative route Intravenous injection Intravenous injection
Side effects Fatigue, nausea, musculoskeletal pain, hemorrhage, hepatotoxicity Neutropenia, diarrhea, nausea, fatigue, anemia, vomiting
Contraindications Known hypersensitivity to trastuzumab emtansine or any of its excipients Known hypersensitivity to sacituzumab govitecan-hziy or any of its components
Drug class Antibody-drug conjugate Antibody-drug conjugate
Manufacturer Genentech (Roche) Gilead Sciences, Inc.

Efficacy

Kadcyla (Trastuzumab Emtansine) for Breast Cancer

Kadcyla (trastuzumab emtansine) is a targeted therapy drug used in the treatment of HER2-positive breast cancer. HER2 is a protein that can promote the growth of cancer cells. In some cancers, notably breast cancer, HER2 is overexpressed, leading to cancer growth. Kadcyla is a combination of trastuzumab, a monoclonal antibody that targets the HER2 protein, and a chemotherapy drug called DM1 (emtansine), which is attached to the antibody. This allows for the direct delivery of the chemotherapy to the cancer cells, sparing normal cells and potentially reducing some chemotherapy side effects.

The efficacy of Kadcyla has been demonstrated in several clinical trials. One pivotal trial that led to its approval was the EMILIA study, which showed that patients with HER2-positive metastatic breast cancer who were treated with Kadcyla had a significant improvement in median progression-free survival compared to those who received lapatinib plus capecitabine, another standard treatment. Furthermore, Kadcyla also showed an increase in overall survival in this patient population. These results have confirmed the role of Kadcyla as an important treatment option for patients with advanced HER2-positive breast cancer.

Trodelvy (Sacituzumab Govitecan-hziy) for Breast Cancer

Trodelvy (sacituzumab govitecan-hziy) is another innovative treatment option for patients with breast cancer, specifically for those with triple-negative breast cancer (TNBC), which is a type of cancer that does not express the genes for estrogen receptor (ER), progesterone receptor (PR), or HER2. Trodelvy is an antibody-drug conjugate which combines a monoclonal antibody that targets the Trop-2 antigen, a protein frequently overexpressed in many epithelial cancers, including TNBC, with a potent chemotherapy drug, SN-38.

The approval of Trodelvy was based on the results of clinical trials that showed a significant benefit in patients with metastatic TNBC who had received at least two prior therapies for metastatic disease. In a phase III trial, Trodelvy significantly improved progression-free survival and overall survival compared to standard single-agent chemotherapy. This marked an important advance in the treatment of TNBC, an aggressive form of breast cancer that previously had limited effective treatment options. Trodelvy's ability to target and deliver chemotherapy directly to cancer cells offers a new hope for patients with this challenging diagnosis.

Regulatory Agency Approvals

Kadcyla
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Trodelvy
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Kadcyla or Trodelvy today

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

How it works

Make an enquiry

Choose the medicine you want to buy, answer a couple of questions, and upload your prescription to speed things up. We’ll get back to you within 24 hours.

Breeze through the paperwork

We'll guide you through the required documents for importing unapproved medicine, ensuring you have all the necessary information.

Get a personalized quote

We’ll prepare a quote for you, including medicine costs and any shipping, administrative, or import fees that may apply.

Receive your medicine

Accept the quote and we’ll handle the rest - sourcing and safely delivering your medicine.

Some text on this page has been automatically generated. Speak to your physician before you start a new treatment or medication.

Let's talk

If you have any questions, call us or send us a message through WhatsApp or email:

Contact us
US 0