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The Phase 3 MAVORIC trial (NCT01728805) compared Mogamulizumab and Vorinostat in 372 patients with relapsed/refractory mycosis fungoides (MF) or Sézary syndrome (SS) who had failed previous systemic treatment (≥1).
Mycosis fungoides
The purpose of this post-mortem analysis was to evaluate the impact of the underlying blood tumor burden on the patient's responsiveness to Mogamulizumab
According to the results of flow cytometry, the test patients were divided into three levels of low, medium and high tumor burden (B0[n=126], B1[n=62], B2[n=184]), and the patients in each group were evaluated PFS, ORR, time before second treatment (TTNT), skin reactivity and safety
Basic tumor burden group details
Basic tumor burden group detailsCompared with vorinostat, Mogamulizumab significantly prolonged the PFS of patients of all grades, especially those of B1 and B2 grades
Compared with vorinostat, Mogamulizumab significantly prolonged the PFS of patients in each grade, especially in patients with grades B1 and B2.
PFS of patients in the two treatment groups
PFS of patients in the two treatment groupsThe TTNT of grade B1 and B2 patients treated with Mogamulizumab was also significantly longer than that of patients treated with vorinostat (B1: 12.
The TTNT of grade B1 and B2 patients treated with Mogamulizumab was also significantly longer than that of patients treated with vorinostat.
Changes in mSWAT of patients in each grade
Changes in mSWAT of patients in each gradeIn the mogamulizumab treatment arm, 82 patients (43.
The CD4+CD26-cell count and CD4:CD8 ratio of patients treated with Mogamulizumab in each group decreased rapidly and continuously
In summary, this post-mortem analysis showed that for patients with MF and SS classified as B1 and B2 blood involvement, Mogamulizumab has greater clinical benefit than vorinostat
For patients with MF and SS classified as B1 and B2 blood involvement, Mogamulizumab has greater clinical benefit than vorinostat.
Original source:
Cowan R,Scarisbrick JJ,Zinzani PL et al.
Efficacy and safety of mogamulizumab by patient baseline blood tumour burden: a post hoc analysis of the MAVORIC trial
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