How long can you stay on Imbruvica (ibrutinib)?
- Imbruvica is usually given until disease progression or unacceptable toxicity occurs, or in the case of graft vs host disease, recurrence of an underlying malignancy.
- The average duration of Imbruvica therapy in CLL clinical trials has been around 41 months (range, 2–51 months).
Imbruvica (ibrutinib) is usually continued indefinitely if it is being well tolerated, there is limited disease progression, and toxicity has not occurred.
In some people, very good partial clinical responses may occur within three to six months.
However, most people are kept on Imbruvica indefinitely regardless of clinical response. This is a common treatment strategy for people with certain types of leukemia and solid tumors because often when the treatment agent is stopped, symptoms can reappear and lymph nodes enlarge within a relatively short period, particularly if patients have not been taking Imbruvica for very long or if they have tried many other previous treatments.
The average duration of Imbruvica therapy in clinical trials has been around 41 months (range, 2–51 months). In people who have stopped Imbruvica, the average survival after treatment discontinuation was 8 months.
What is the dosage of Imbruvica?
The recommended starting dose for Imbruvica varies depending on the condition being treated, but examples include:
- Mantle cell lymphoma: 560mg once daily
- Marginal zone lymphoma: 560mg once daily
- Waldenstrom's macroglobulinemia: 420mg once daily
- Chronic lymphocytic leukemia (CLL): 420mg once daily
- Small lymphocytic lymphoma: 420mg once daily
- Chronic graft-versus-host disease: 420mg once daily.
Dosages may need reducing if toxicities occur. Imbruvica is usually given until disease progression or unacceptable toxicity occurs, or in the case of graft vs host disease, recurrence of an underlying malignancy.
What are the most common side effects with Imbruvica?
The most common side effects reported with Imbruvica include:
- Back pain
- Chest pain, atrial fibrillation, atrial flutter
- High blood pressure
- Lowered blood counts
- Muscle aches
- Blood in the urine.
These are typically noted more at the beginning of therapy, but for most people, they resolve quickly with time and are often non-existent within 2-3 months. Older people are more at risk of side effects including bruising. In general, Imbruvica is usually well tolerated.
What is Imbruvica?
Imbruvica is a targeted medicine that works by inhibiting the enzyme Bruton tyrosine kinase (BTK), which is part of a crucial signaling pathway in certain cancers, especially B-cell leukemias and lymphomas.
By blocking this pathway Imbruvica triggers the death of cancer cells. Imbruvica may be used in the treatment of
- Mantle cell lymphoma
- Marginal zone lymphoma
- Waldenstrom's macroglobulinemia
- Chronic lymphocytic leukemia
- Small lymphocytic lymphoma.
Imbruvica may also be used to treat chronic graft-versus-host disease.
- Imbruvica (ibrutinib) capsules [Package Insert] Pharmacyclics LLC, an AbbVie Company and Janssen Biotech, Inc https://www.drugs.com/pro/imbruvica.html
- You and I support program. Pharmacyclics LLC, an AbbVie Company and Janssen Biotech, Inc https://youandisupport.com/
- Preetesh J, Keating M, Wierda w, et al. Long-term Follow-up of Treatment with Ibrutinib and Rituximab in Patients with High-Risk Chronic Lymphocytic Leukemia. Clinical Cancer Research. October 19, 2016; DOI: 10.1158/1078-0432.CCR-16-1948
- Top 15 Questions About Ibrutinib CLL Society June 2016. https://cllsociety.org/2016/06/top-15-questions-ibrutinib/
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