Polivy (polatuzumab vedotin-piiq) vs Lunsumio (mosunetuzumab-axgb)

Polivy (polatuzumab vedotin-piiq) vs Lunsumio (mosunetuzumab-axgb)

Polivy (polatuzumab vedotin-piiq) is an antibody-drug conjugate specifically targeting CD79b, a protein associated with B-cell non-Hodgkin lymphoma, and is used in combination with other drugs for the treatment of adults with relapsed or refractory diffuse large B-cell lymphoma. Lunsumio (mosunetuzumab-axgb), on the other hand, is a bispecific T-cell engager that redirects the patient's own T-cells to engage and eliminate B-cells, and is used for the treatment of adult patients with relapsed or refractory follicular lymphoma. When deciding which medicine is right for an individual, it is crucial to consider the specific type of lymphoma, the patient's previous treatments and responses, and the unique safety profiles and mechanisms of action of each medication, as well as consulting with a healthcare professional.

Difference between Polivy and Lunsumio

Metric Polivy (polatuzumab vedotin-piiq) Lunsumio (mosunetuzumab-axgb)
Generic name Polatuzumab vedotin-piiq Mosunetuzumab-axgb
Indications Treatment of relapsed or refractory diffuse large B-cell lymphoma Treatment of relapsed or refractory follicular lymphoma
Mechanism of action Antibody-drug conjugate targeting CD79b T-cell engaging bispecific antibody targeting CD20 and CD3
Brand names Polivy Lunsumio
Administrative route Intravenous infusion Intravenous infusion
Side effects Neutropenia, anemia, thrombocytopenia, peripheral neuropathy, fatigue Cytokine release syndrome, infections, fatigue, diarrhea, rash
Contraindications Hypersensitivity to polatuzumab vedotin-piiq or any of its excipients Hypersensitivity to mosunetuzumab-axgb or any of its excipients
Drug class Antibody-drug conjugate T-cell engaging bispecific antibody
Manufacturer Genentech, Inc. Genentech, Inc.

Efficacy

Polivy (polatuzumab vedotin-piiq) Efficacy in Treating Lymphoma

Polivy (polatuzumab vedotin-piiq) is a targeted cancer medicine that is used in combination with other drugs to treat certain types of non-Hodgkin lymphoma. Specifically, it is indicated for the treatment of adults with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), which is the most common type of non-Hodgkin lymphoma. The efficacy of Polivy was evaluated in a clinical study that included patients who had relapsed after or were refractory to at least two prior therapies. When used in combination with bendamustine and a rituximab product, Polivy has shown a significant improvement in overall response rate (ORR) and complete response rate (CRR) compared to treatments without Polivy.

In the pivotal trial that led to its approval, patients treated with the Polivy combination therapy demonstrated a higher complete response rate compared to those who received only bendamustine and rituximab. Furthermore, the median duration of response for patients who achieved a complete or partial response was significantly longer for those who received the Polivy combination. These results suggest that Polivy, when used as part of a combination regimen, can be an effective treatment option for patients with relapsed or refractory DLBCL.

Lunsumio (mosunetuzumab-axgb) Efficacy in Treating Lymphoma

Lunsumio (mosunetuzumab-axgb) is a bispecific antibody designed for the treatment of certain types of B-cell non-Hodgkin lymphoma. It targets two different proteins found on the surface of cells: CD20 on B cells and CD3 on T cells. By bringing these cells together, Lunsumio helps the body's immune system to attack and kill the cancerous B cells. The efficacy of Lunsumio has been evaluated in patients with relapsed or refractory follicular lymphoma, who have received at least two prior systemic therapies.

In clinical trials, Lunsumio has demonstrated promising efficacy in inducing responses in a significant proportion of patients with relapsed or refractory follicular lymphoma. The ORR and CRR were notably high, with many patients achieving a complete response. Additionally, the duration of response observed in these studies indicates that Lunsumio can provide a durable remission for some patients. These findings support the potential of Lunsumio as a new therapeutic option for patients with this challenging form of lymphoma, expanding the arsenal of treatments available to combat this disease.

Regulatory Agency Approvals

Polivy
  • Food and Drug Administration (FDA), USA
  • 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 Polivy or Lunsumio today

If Polivy 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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