Monjuvi (tafasitamab-cxix) vs Zynlonta (loncastuximab tesirine-lpyl)

Monjuvi (tafasitamab-cxix) vs Zynlonta (loncastuximab tesirine-lpyl)

Monjuvi (tafasitamab-cxix) is a CD19-directed cytolytic antibody indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), to be used in combination with lenalidomide, followed by Monjuvi monotherapy. Zynlonta (loncastuximab tesirine-lpyl) is an antibody-drug conjugate also indicated for the treatment of adult patients with relapsed or refractory DLBCL after two or more lines of systemic therapy. When deciding between the two, a patient should consider factors such as the specific mechanism of action, the treatment regimen, potential side effects, and any previous therapies they have received, in consultation with their healthcare provider.

Difference between Monjuvi and Zynlonta

Metric Monjuvi (tafasitamab-cxix) Zynlonta (loncastuximab tesirine-lpyl)
Generic name Tafasitamab-cxix Loncastuximab tesirine-lpyl
Indications For the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) For the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy
Mechanism of action CD19-directed cytolytic antibody CD19-directed cytolytic antibody conjugated to a cytotoxic agent
Brand names Monjuvi Zynlonta
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, anemia, diarrhea, cough, fever, etc. Fatigue, thrombocytopenia, musculoskeletal pain, nausea, etc.
Contraindications Known hypersensitivity to tafasitamab or any of its excipients Known hypersensitivity to loncastuximab tesirine-lpyl or any of its excipients
Drug class Antineoplastic agent, anti-CD19 monoclonal antibody Antineoplastic agent, antibody-drug conjugate
Manufacturer MorphoSys AG ADC Therapeutics SA

Efficacy

Efficacy of Monjuvi (tafasitamab-cxix) for Lymphoma

Monjuvi (tafasitamab-cxix) is a CD19-directed cytolytic antibody indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). This medication is not indicated for the treatment of patients with primary central nervous system lymphoma. The efficacy of Monjuvi, in combination with lenalidomide, was evaluated in a multicenter, single-arm, open-label trial known as the L-MIND study. Patients treated with this combination showed a meaningful improvement in overall response rate (ORR), with a significant proportion achieving complete response (CR). The duration of response (DOR) for these patients varied, with some experiencing prolonged responses, indicating a potential for durable remission in a subset of the treated population.

Efficacy of Zynlonta (loncastuximab tesirine-lpyl) for Lymphoma

Zynlonta (loncastuximab tesirine-lpyl) is an antibody-drug conjugate specifically directed against CD19, a protein expressed on the surface of B-cells, which are often implicated in non-Hodgkin lymphoma (NHL), including DLBCL. Zynlonta has been approved for the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy. The efficacy of Zynlonta was primarily demonstrated in a pivotal Phase 2, single-arm, open-label, multicenter trial known as LOTIS-2. The trial results showed a significant ORR with a notable CR rate in heavily pretreated patients. The median DOR, as well as the median progression-free survival (PFS) and overall survival (OS), were also evaluated to assess the benefit of the treatment.

Comparative Efficacy in Lymphoma Treatment

While both Monjuvi and Zynlonta target CD19 and are used in similar patient populations with relapsed or refractory DLBCL, their mechanisms of action and formulations differ. Monjuvi is used in combination with lenalidomide, an immunomodulatory agent, whereas Zynlonta is a standalone therapy that combines a targeted antibody with a cytotoxic agent. Direct comparative efficacy data between Monjuvi and Zynlonta are not typically available, as head-to-head clinical trials have not been conducted. Therefore, the choice of therapy may depend on individual patient characteristics, prior treatment responses, and the treating physician's clinical judgment.

Considerations for Treatment Selection

When considering the use of Monjuvi or Zynlonta for the treatment of lymphoma, it is important to evaluate the patient's overall health, previous treatments, and potential for adverse effects. Both treatments offer a targeted approach for relapsed or refractory DLBCL, which is often challenging to treat. The decision to use either Monjuvi or Zynlonta should be made in the context of a comprehensive treatment plan, taking into account the most current clinical trial data and treatment guidelines. As with all therapies, ongoing monitoring of treatment efficacy and safety is crucial to optimize patient outcomes.

Regulatory Agency Approvals

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

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If Monjuvi or Zynlonta 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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