Calquence (acalabrutinib) vs Columvi (glofitamab-gxbm)

Calquence (acalabrutinib) vs Columvi (glofitamab-gxbm)

Calquence (acalabrutinib) is a Bruton's tyrosine kinase (BTK) inhibitor used primarily in the treatment of certain types of B-cell malignancies, such as chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL). On the other hand, Glofitamab (under the investigational name and not yet approved with the trade name Columvi as of the knowledge cutoff in 2023) is a bispecific CD20xCD3 T-cell engager designed for the treatment of relapsed or refractory B-cell non-Hodgkin lymphomas. When deciding between these medications, a patient should consider the specific type of lymphoma they have, the stage of the disease, previous treatments, potential side effects, and the advice of their healthcare provider, as each medication targets different mechanisms of action and is indicated for different patient populations.

Difference between Calquence and Columvi

Metric Calquence (acalabrutinib) Columvi (glofitamab-gxbm)
Generic name Acalabrutinib Glofitamab-gxbm
Indications Chronic lymphocytic leukemia (CLL), Small lymphocytic lymphoma (SLL), Mantle cell lymphoma (MCL) Currently under investigation, potential use in B-cell non-Hodgkin lymphoma
Mechanism of action Bruton's tyrosine kinase (BTK) inhibitor Bispecific monoclonal antibody targeting CD20 on B-cells and CD3 on T-cells
Brand names Calquence Columvi (not yet commercially available)
Administrative route Oral Intravenous
Side effects Headache, diarrhea, muscle pain, bruising, fatigue, anemia Not fully characterized, may include cytokine release syndrome, infusion-related reactions
Contraindications Hypersensitivity to acalabrutinib or its excipients, severe hepatic impairment Not fully established, likely hypersensitivity to glofitamab or its excipients
Drug class Small molecule kinase inhibitor Monoclonal antibody
Manufacturer AstraZeneca Roche

Efficacy

Calquence (Acalabrutinib) Efficacy in Lymphoma

Calquence (acalabrutinib) is a Bruton's tyrosine kinase (BTK) inhibitor that has shown efficacy in treating certain types of lymphoma, particularly mantle cell lymphoma (MCL) and chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). In clinical trials, acalabrutinib has demonstrated a high overall response rate in patients with relapsed or refractory MCL. The drug has been approved by regulatory agencies for these indications due to its ability to block BTK signaling, which is essential for the growth and survival of malignant B cells.

In clinical settings, acalabrutinib has been favored for its efficacy and a tolerable safety profile. Studies have shown that the progression-free survival (PFS) rates are significantly improved in patients treated with acalabrutinib compared to alternative treatments. The drug's efficacy in CLL/SLL has also been notable, with a substantial proportion of patients achieving partial or complete remission. The effectiveness of acalabrutinib in these lymphoma subtypes has led to its consideration as a frontline treatment option.

Columvi (Glofitamab-gxbm) Efficacy in Lymphoma

Columvi (glofitamab-gxbm) is an investigational bispecific monoclonal antibody designed to target CD20 on B cells and CD3 on T cells, thereby engaging the patient's own immune system to attack B-cell lymphomas. While not yet approved, glofitamab is being studied in clinical trials for its potential to treat various B-cell lymphomas, including non-Hodgkin's lymphoma (NHL). Early clinical trial results have shown promising efficacy in heavily pretreated patients with relapsed or refractory NHL, including those who have not responded to or have relapsed after CAR T-cell therapies.

Initial data from these trials suggest that glofitamab can induce complete responses in a significant number of patients, with some experiencing durable remissions. The dual targeting mechanism of glofitamab is thought to enhance its ability to eliminate lymphoma cells compared to traditional monoclonal antibodies. Ongoing studies continue to evaluate the long-term efficacy and safety of glofitamab in a broader lymphoma population, with the hope of providing a new therapeutic option for patients with limited treatment choices.

Regulatory Agency Approvals

Calquence
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
Columvi
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Calquence or Columvi today

If Calquence or Columvi are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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