Understanding Calquence (Acalabrutinib)
Calquence (acalabrutinib) is a prescription oral medication that targets Bruton's tyrosine kinase (BTK), a protein important for the growth and survival of certain cancer cells. It is a targeted therapy, distinguishing it from traditional chemotherapy. Calquence is classified as a kinase inhibitor, specifically targeting BTK. Manufactured by AstraZeneca, it is available as a 100 mg oral tablet taken twice daily.
How Calquence Works (Mechanism of Action)
Calquence works by blocking BTK, a protein critical for the B-cell receptor signaling pathway. In blood cancers like chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL), this pathway is essential for malignant B-cells to grow and survive. By binding to BTK, Calquence disrupts this signaling, leading to the death of cancerous B-cells. Calquence is a highly selective BTK inhibitor with minimal off-target activity, which may result in a more favorable side effect profile compared to older BTK inhibitors.
What Conditions Does Calquence Treat?
Calquence is approved for treating specific adult B-cell malignancies. Its use and combinations depend on the patient's condition and history.
Calquence is indicated for:
- Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL): For adult patients with CLL or SLL.
- Mantle Cell Lymphoma (MCL): For adult patients with previously treated MCL, or in combination with bendamustine and rituximab for previously untreated MCL patients not eligible for autologous hematopoietic stem cell transplantation.
Dosage and Administration
The usual dose is one 100 mg Calquence tablet taken orally twice daily, approximately 12 hours apart. It should be swallowed whole with water, and can be taken with or without food. Treatment continues until disease progression or unacceptable side effects occur. Consistent dosing is important for continuous BTK inhibition.
Side Effects of Calquence
Calquence can cause side effects. {Link: Drugs.com https://www.drugs.com/calquence.html} provides information on common side effects, which may include headache, diarrhea, fatigue, musculoskeletal pain, bruising, nausea, and upper respiratory tract infection. Serious side effects like infections, hemorrhage, decreased blood cell counts, cardiac arrhythmias, and a risk of developing other cancers have also been reported. Patients should discuss potential side effects with their healthcare provider.
Comparing Calquence to Other BTK Inhibitors
Calquence, a second-generation BTK inhibitor, is often compared to the first-generation inhibitor ibrutinib and another second-generation inhibitor, zanubrutinib. Information on BTK selectivity, mechanism, cardiovascular risks, common side effects, tolerability, and efficacy for these drugs can be found on {Link: Drugs.com https://www.drugs.com/calquence.html}.
Important Warnings and Drug Interactions
Inform your doctor about all medications and supplements before starting Calquence.
- CYP3A Interactions: Calquence is metabolized by CYP3A. Strong inhibitors can increase Calquence levels (e.g., ketoconazole), while strong inducers can decrease them (e.g., rifampin).
- Gastric Acid Reducers: Avoid proton pump inhibitors. Take H2-receptor antagonists at a different time.
- Blood Thinners: Concomitant use can increase bleeding risk.
- Herbal Supplements: Avoid St. John's wort.
- Surgery: Your doctor may recommend stopping Calquence before and after surgery to reduce bleeding risk.
Conclusion
Calquence offers a targeted treatment option for specific B-cell malignancies, acting as a BTK inhibitor to disrupt cancer cell growth and survival. It is used for conditions like CLL, SLL, and MCL. While generally well-tolerated, potential side effects and drug interactions require careful medical monitoring. Ongoing research continues to evaluate its use and compare it to other treatments. Treatment decisions should be made in consultation with a healthcare provider. More information is available on the {Link: FDA.gov https://www.fda.gov/drugs/resources-information-approved-drugs/project-orbis-fda-approves-acalabrutinib-cll-and-sll}.