Calquence (acalabrutinib) vs Lunsumio (mosunetuzumab-axgb)

Calquence (acalabrutinib) vs Lunsumio (mosunetuzumab-axgb)

Calquence (acalabrutinib) is a small molecule Bruton's tyrosine kinase (BTK) inhibitor used primarily for the treatment of certain types of B-cell malignancies, such as chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL). Lunsumio (mosunetuzumab-axgb), on the other hand, is a bispecific T-cell engager antibody indicated for the treatment of relapsed or refractory follicular lymphoma, which works by redirecting the body's own T-cells to engage and eliminate B-cells. The choice between Calquence and Lunsumio would depend on the specific type and stage of lymphoma, previous treatments, patient's overall health, potential side effects, and the recommendation of an oncologist.

Difference between Calquence and Lunsumio

Metric Calquence (acalabrutinib) Lunsumio (mosunetuzumab-axgb)
Generic name Acalabrutinib Mosunetuzumab-axgb
Indications Chronic lymphocytic leukemia (CLL), Small lymphocytic lymphoma (SLL), Mantle cell lymphoma (MCL) Follicular lymphoma
Mechanism of action Bruton's tyrosine kinase (BTK) inhibitor Bispecific T-cell engager antibody
Brand names Calquence Lunsumio
Administrative route Oral Intravenous
Side effects Headache, diarrhea, muscle pain, bruising, fatigue, and others Cytokine release syndrome, infections, fatigue, diarrhea, and others
Contraindications History of serious hypersensitivity to acalabrutinib or its excipients No known contraindications
Drug class Small molecule kinase inhibitor Monoclonal antibody
Manufacturer AstraZeneca Genentech, a member of the Roche Group

Efficacy

Calquence (Acalabrutinib) Efficacy in Lymphoma

Calquence, also known by its generic name acalabrutinib, is a novel Bruton's tyrosine kinase (BTK) inhibitor that has shown efficacy in the treatment of certain types of lymphoma. Specifically, acalabrutinib has been approved for the treatment of mantle cell lymphoma (MCL) in patients who have received at least one prior therapy. Clinical trials have demonstrated that acalabrutinib can lead to high response rates in relapsed or refractory MCL, with a significant proportion of patients achieving complete remission. The drug's mechanism of action involves the selective inhibition of BTK, a key molecule in the B-cell receptor signaling pathway, which is critical for the survival and proliferation of malignant B cells.

In addition to MCL, acalabrutinib is being investigated for its potential use in other types of B-cell lymphomas, including chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL), where it has also shown promising results. The efficacy of acalabrutinib in these lymphomas is reflected in the overall response rates and duration of response observed in clinical trials, with some patients experiencing long-term remissions.

Lunsumio (Mosunetuzumab-axgb) Efficacy in Lymphoma

Lunsumio, with the generic name mosunetuzumab-axgb, is a bispecific T-cell engager antibody that has been designed to target CD20 on B cells and CD3 on T cells, thereby redirecting T cells to engage and eliminate B-cell lymphomas. Mosunetuzumab-axgb has shown efficacy in the treatment of non-Hodgkin lymphoma (NHL), including both relapsed or refractory follicular lymphoma and diffuse large B-cell lymphoma (DLBCL). Clinical studies have reported that mosunetuzumab-axgb can induce complete remissions in a significant number of patients with relapsed or refractory NHL, including those who have not responded to or have relapsed after multiple prior treatments, including CAR T-cell therapies.

The clinical efficacy of mosunetuzumab-axgb is particularly noteworthy in follicular lymphoma, where it has demonstrated a high complete response rate with durable remissions. The treatment is generally well-tolerated, and its novel mechanism of action offers a new therapeutic option for patients with B-cell lymphomas who have limited treatment choices. As with any therapy, ongoing studies continue to evaluate the long-term efficacy and safety profile of mosunetuzumab-axgb in a broader patient population.

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
Lunsumio
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Calquence or Lunsumio today

If Calquence or Lunsumio 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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