Therapies

Ado-trastuzumab emtansine

Kadcyla

This post is under:

Oncofocus Test Kit
includes suggestions for Ado-trastuzumab emtansine

Oncofocus is the world’s most comprehensive precision oncology test that precisely identifies the right drug for your cancer thereby increasing your chances of successful treatment.

Discover Oncofocus Today Do you want to order now? Request a test.

SUMMARY

Company: Genentech
Approval Status: FDA Approved February 2013
Specific Treatments: HER2-positive metastatic breast cancer
Drug: Ado-trastuzumab emtansine

 

GENERAL INFORMATION

Kadcyla (ado-trastuzumab emtansine) is a HER2-targeted antibody-drug conjugate. Upon binding to the HER2 receptor, ado-trastuzumab emtansine results in intracellular release of DM1-containing cytotoxic catabolites. Binding of DM1 to tubulin disrupts microtubule networks in the cell, which results in cell cycle arrest and apoptotic cell death.

Kadcyla is specifically indicated for the treatment of patients with HER2-positive, metastatic breast cancerwho previously received trastuzumab and a taxane, separately or in combination.

Kadcyla is supplied as a solution designed for intravenous infusion. The recommended initial dose is 3.6 mg/kg given as an intravenous infusion every 3 weeks (21-day cycle) until disease progression or unacceptable toxicity. Do not administer Kadcyla at doses greater than 3.6 mg/kg. First infusion: Administer infusion over 90 minutes. Patients should be observed during the infusion and for at least 90 minutes following the initial dose for fever, chills, or other infusion related reactions. Subsequent infusions: Administer over 30 minutes if prior infusions were well tolerated. Patients should be observed during the infusion and for at least 30 minutes after infusion.

 

CLINICAL RESULTS

FDA Approval

The FDA approval of Kadcyla was based on a randomized, multicenter, open-label trial of 991 subjects with HER2-positive, unresectable locally advanced or metastatic breast cancer. All subjects had received prior taxane and trastuzumab-based therapy. The subjects were randomly assigned to receive Kadcyla (3.6 mg/kg on Day 1 of a 21-day cycle) or lapatinib (1250 mg/day orally once per day of a 21-day cycle) plus capecitabine (1000 mg/m2 orally twice daily on Days 1-14 of a 21-day cycle). Treatment continued until disease progression, withdrawal of consent, or unacceptable toxicity. The co-primary efficacy endpoints of the study were progression-free survival (PFS) based on tumor response assessments by an independent review committee and overall survival (OS). The subjects treated with Kadcyla had a median progression-free survival of 9.6 months compared to 6.4 months in patients treated with lapatinib plus capecitabine. The median overall survival was 30.9 months in the Kadcyla group and 25.1 months in the lapatinib plus capecitabine group.

 

SIDE EFFECTS

Adverse events associated with the use of Kadcyla may include, but are not limited to, the following:

  • fatigue
  • nausea
  • musculoskeletal pain
  • thrombocytopenia
  • headache
  • increased transaminases
  • constipation

 

MECHANISM OF ACTION

Ado-trastuzumab emtansine is a HER2-targeted antibody-drug conjugate. The antibody is the humanized anti-HER2 IgG1, trastuzumab. The small molecule cytotoxin, DM1, is a microtubule inhibitor. Upon binding to sub-domain IV of the HER2 receptor, ado-trastuzumab emtansine undergoes receptor-mediated internalization and subsequent lysosomal degradation, resulting in intracellular release of DM1-containing cytotoxic catabolites. Binding of DM1 to tubulin disrupts microtubule networks in the cell, which results in cell cycle arrest and apoptotic cell death.

Source: centerwatch