Solid tumours that display a Neurotrophic Tyrosine Receptor Kinase (NTRK) gene fusion

Active Ingredient: Larotrectinib

Indication for Larotrectinib

Population group: only adults (18 - 65 years old)

Larotrectinib as monotherapy is indicated for the treatment of adult and paediatric patients with solid tumours that display a Neurotrophic Tyrosine Receptor Kinase (NTRK) gene fusion,

  • who have a disease that is locally advanced, metastatic or where surgical resection is likely to result in severe morbidity, and
  • who have no satisfactory treatment options.

For this indication, competent medicine agencies globally authorize below treatments:

200 mg in 2 divided doses daily

Route of admnistration

Oral

Defined daily dose

200 - 200 mg

Dosage regimen

From 100 To 100 mg 2 time(s) per day every day

Detailed description

The recommended dose in adults is 100 mg larotrectinib twice daily, until disease progression or until unacceptable toxicity occurs.

Missed dose

If a dose is missed, the patient should not take two doses at the same time to make up for a missed dose. Patients should take the next dose at the next scheduled time. If the patient vomits after taking a dose, the patient should not take an additional dose to make up for vomiting.

Dose modification

For all Grade 2 adverse reactions, continued dosing may be appropriate, though close monitoring to ensure no worsening of the toxicity is advised. Patients with Grade 2 ALT and/or AST increases, should be followed with serial laboratory evaluations every one to two weeks after the observation of Grade 2 toxicity until resolved to establish whether a dose interruption or reduction is required.

For Grade 3 or 4 adverse reactions:

  • Larotrectinib should be withheld until the adverse reaction resolves or improves to baseline or Grade 1. Resume at the next dose modification if resolution occurs within 4 weeks.
  • Larotrectinib should be permanently discontinued if an adverse reaction does not resolve within 4 weeks.

The recommended dose modifications for larotrectinib for adverse reactions are provided in the following table.

Recommended dose modifications for larotrectinib for adverse reactions:

Dose modificationAdult and paediatric patients with body surface area of at least 1.0 m²Paediatric patients with body surface area less than 1.0 m²
First 75 mg twice daily 75 mg/m² twice daily
Second 50 mg twice daily 50 mg/m² twice daily
Third100 mg once daily 25 mg/m² twice dailya

a Paediatric patients on 25 mg/m² twice daily should remain on this dose even if body surface area becomes greater 1.0 m² during the treatment. Maximum dose should be 25 mg twice daily at the third dose modification.

Larotrectinib should be permanently discontinued in patients who are unable to tolerate larotrectinib after three dose modifications.

Dosage considerations

Larotrectinib can be taken with or without food but should not be taken with grapefruit or grapefruit juice.

Active ingredient

Larotrectinib

Larotrectinib is an adenosine triphosphate (ATP)-competitive and selective tropomyosin receptor kinase (TRK) inhibitor. The TRK family of proteins, TRKA, TRKB, and TRKC, is encoded by NTRK1, NTRK2 and NTRK3 genes. Larotrectinib was rationally designed to avoid activity with off-target kinases. It is indicated for the treatment of adult and paediatric patients with solid tumours that display a Neurotrophic Tyrosine Receptor Kinase (NTRK) gene fusion.

Read more about Larotrectinib

Related medicines

Develop a tailored medication plan for your case, considering factors such as age, gender, and health history

Ask the Reasoner

Liability Disclaimer : RxReasoner has utilized reasonable care in providing content and services that are accurate, complete and up to date. However, RxReasoner does not accept any responsibility or liability about it. The content and services of RxReasoner are for informational purposes only and they are not intended to be a substitute for the knowledge, expertise, skill, and judgment of physicians, pharmacists, nurses, or other healthcare professionals involved in patient care. RxReasoner offers no medical advice. Users are responsible for the use of the provided content. A shown indication or treatment should not be construed to indicate that the medication is safe, appropriate, or effective in any given patient or under any particular circumstances. The absence of an indication or treatment should not roule out the existence of other appropriate medications. Always seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition or medicament. RxReasoner is not liable for any damages allegedly sustained arising out of the use of its content and services.