Zynlonta (loncastuximab tesirine-lpyl) vs Jaypirca (pirtobrutinib)

Zynlonta (loncastuximab tesirine-lpyl) vs Jaypirca (pirtobrutinib)

Zynlonta (loncastuximab tesirine-lpyl) is an antibody-drug conjugate specifically indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), a type of non-Hodgkin lymphoma. Jaypirca (pirtobrutinib) is a Bruton's tyrosine kinase (BTK) inhibitor designed for the treatment of mantle cell lymphoma and other B-cell malignancies, particularly in cases where patients have received prior therapies that have failed or are no longer effective. When deciding which medicine is right for an individual, it is crucial to consider the specific type of lymphoma being treated, previous treatments, and the patient's overall health profile, as Zynlonta and Jaypirca are targeted toward different lymphoma subtypes and have distinct mechanisms of action and side effect profiles.

Difference between Zynlonta and Jaypirca

Metric Zynlonta (loncastuximab tesirine-lpyl) Jaypirca (pirtobrutinib)
Generic name Loncastuximab tesirine-lpyl Pirtobrutinib
Indications Relapsed or refractory large B-cell lymphoma Relapsed or refractory B-cell malignancies
Mechanism of action CD19-directed antibody and alkylating agent conjugate Bruton's tyrosine kinase (BTK) inhibitor
Brand names Zynlonta Jaypirca
Administrative route Intravenous Oral
Side effects Fatigue, anemia, thrombocytopenia, neutropenia, etc. Fatigue, diarrhea, muscle and joint pain, rash, etc.
Contraindications Hypersensitivity to loncastuximab tesirine-lpyl or excipients Hypersensitivity to pirtobrutinib or any component of the formulation
Drug class Antibody-drug conjugate Bruton's tyrosine kinase inhibitor
Manufacturer ADC Therapeutics Loxo Oncology at Lilly

Efficacy

Efficacy of Zynlonta (loncastuximab tesirine-lpyl) in Lymphoma

Zynlonta (loncastuximab tesirine-lpyl) is a CD19-directed antibody and alkylating agent conjugate indicated 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 in lymphoma was evaluated in a multicenter, single-arm, open-label trial known as LOTIS-2. Patients treated with Zynlonta demonstrated a significant response rate, with a notable percentage achieving a complete response. The results were compelling enough to grant accelerated approval by the U.S. Food and Drug Administration (FDA), offering a new treatment option for patients with limited alternatives due to the aggressive nature of relapsed or refractory large B-cell lymphoma.

Efficacy of Jaypirca (pirtobrutinib) in Lymphoma

Jaypirca (pirtobrutinib) is a highly selective and non-covalent Bruton's tyrosine kinase (BTK) inhibitor. While it is not yet approved by the FDA, its efficacy in treating lymphoma, particularly B-cell malignancies, has been the subject of clinical research. In early clinical trials, pirtobrutinib has shown promising results in patients with B-cell malignancies, including those who have been previously treated with other BTK inhibitors. The drug is designed to overcome resistance to other BTK inhibitors and has been studied in patients with various types of lymphoma, including mantle cell lymphoma and chronic lymphocytic leukemia.

Both Zynlonta and Jaypirca represent advancements in the treatment of lymphoma, offering hope to patients who have exhausted other therapeutic options. As with all medications, the efficacy of these drugs can vary from patient to patient, and their use should be guided by a healthcare professional well-versed in the management of lymphoma. Ongoing clinical trials and post-marketing surveillance continue to provide additional data on the long-term efficacy and safety of these treatments.

It is important for healthcare providers to stay informed about the latest clinical evidence and to consider the individual patient's disease characteristics and prior treatment history when deciding to use these medications. As new data emerge, recommendations for the use of Zynlonta and Jaypirca may evolve, ensuring that patients with lymphoma receive the most effective and personalized care possible.

Regulatory Agency Approvals

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

Access Zynlonta or Jaypirca today

If Zynlonta or Jaypirca 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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