Mogamulizumab-kpkc

(Poteligeo®)

Poteligeo®

Drug updated on 3/28/2024

Dosage FormInjection (intravenous: 20 mg/5 mL (4 mg/mL))
Drug ClassCC chemokine receptor type 4 (CCR4)- directed monoclonal antibodies
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • For the treatment of adult patients with relapsed or refractory mycosis fungoides or Sézary syndrome after at least one prior systemic therapy.

Summary
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  • Mogamulizumab-kpkc (Poteligeo) is indicated for the treatment of adult patients with relapsed or refractory mycosis fungoides or Sézary syndrome after at least one prior systemic therapy.
  • Four systematic reviews/meta-analyses were reviewed to gather information about this drug and its effectiveness in treating these conditions.
  • The National Institute for Health and Care Excellence (NICE) found that mogamulizumab-kpkc showed favorable results in patients with mycosis fungoides and Sézary syndrome, but there was uncertainty due to study design, specifically crossover of patients from a trial called MAVORIC which compared mogamulizumab to vorinostat, not standard care in the NHS.
  • A review examining survival outcomes for Adult T-cell leukemia-lymphoma treated with various therapies found that mogamulizumab was frequently studied and potentially provided longer survival compared to chemotherapy alone; however, future comparisons are needed for clearer insights into treatment efficacy.
  • Another review evaluating safety profile of mogamulizumab concluded it had clinically meaningful antitumor activity with acceptable toxicity when used as monotherapy or combined therapy; common adverse events included lymphopenia, infusion reaction fever rash chills neutropenia anaemia gastrointestinal disorder among others depending on whether it's used alone or combined respectively.
  • In a prospective cohort study conducted at Zagazig University Hospital Egypt between 2017-2022 involving 64 classical Hodgkin lymphoma (CHL) patients divided into EBV-positive & EBV-negative groups,it was observed that EBV-positive CHL patients who expressed mRNAs molecules & end product proteins associated with JAK/STAT & NF-KB pathways were more susceptible to cancer progression.