What is the administration frequency of Kadcyla (ado-trastuzumab emtansine)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: July 18, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Kadcyla Administration Frequency

Kadcyla (ado-trastuzumab emtansine) is administered intravenously at a dose of 3.6 mg/kg every 3 weeks (21-day cycle) until disease progression or unmanageable toxicity. 1

Administration Protocol

The FDA-approved administration schedule for Kadcyla follows a specific protocol:

  • First infusion: Administer over 90 minutes

    • Observe patients during infusion and for at least 90 minutes following the initial dose
    • Monitor for fever, chills, or other infusion-related reactions
  • Subsequent infusions: Administer over 30 minutes if prior infusions were well tolerated

    • Continue observation during infusion and for at least 30 minutes afterward

Duration of Treatment

Treatment duration depends on the indication:

  • Metastatic Breast Cancer (MBC): Continue treatment until disease progression or unmanageable toxicity
  • Early Breast Cancer (EBC): Complete a total of 14 cycles unless disease recurrence or unmanageable toxicity occurs 1

Dose Modifications

Dose modifications may be necessary based on adverse reactions:

  • Do not re-escalate the dose after a reduction
  • If a dose is delayed or missed, administer as soon as possible
  • Maintain the 3-week interval between doses
  • Dose reduction schedule:
    • Starting dose: 3.6 mg/kg
    • First reduction: 3.0 mg/kg
    • Second reduction: 2.4 mg/kg
    • Further reduction needed: Discontinue treatment 1

Important Considerations

  • Patient Selection: Ensure proper patient selection based on HER2 protein overexpression or HER2 gene amplification in tumor specimens
  • Monitoring: Regular cardiac monitoring is essential due to potential cardiotoxicity
  • Toxicity Management: Dose modifications may be required for increased transaminases, hyperbilirubinemia, left ventricular dysfunction, thrombocytopenia, pulmonary toxicity, or peripheral neuropathy 1

Common Side Effects

The most common adverse reactions (>25%) with Kadcyla include:

  • Fatigue
  • Nausea
  • Increased transaminases
  • Musculoskeletal pain
  • Hemorrhage
  • Thrombocytopenia
  • Headache
  • Peripheral neuropathy
  • Arthralgia 2

Kadcyla should not be substituted for or with trastuzumab, as they are different medications with different dosing schedules and safety profiles 1.

References

Research

FDA Approval Summary: Ado-Trastuzumab Emtansine for the Adjuvant Treatment of HER2-positive Early Breast Cancer.

Clinical cancer research : an official journal of the American Association for Cancer Research, 2020

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.