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. 2019 May;104(5):e211-e214.
doi: 10.3324/haematol.2018.205229. Epub 2018 Nov 15.

Ibrutinib for the treatment of relapsed/refractory mantle cell lymphoma: extended 3.5-year follow up from a pooled analysis

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Ibrutinib for the treatment of relapsed/refractory mantle cell lymphoma: extended 3.5-year follow up from a pooled analysis

Simon Rule et al. Haematologica. 2019 May.
No abstract available

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Figures

Figure 1.
Figure 1.
Kaplan-Meier curves of progression-free survival (PFS) and overall survival (OS) in pooled population including the CAN3001 study. (A) Patients with 1 prior line of therapy before ibrutinib treatment had longer median PFS than those with >1 prior line: 25.4 (95%CI: 17.5-57.5) vs. 10.3 (95%CI: 8.1-12.5) months. (B) Patients with 1 prior line of therapy before ibrutinib treatment had longer median overall survival than those with >1 prior line: NR (95%CI: 36.0-NE) versus 22.5 (95%CI: 16.2-26.7) months. CI: confidence interval; mo: months; NE: not estimable; NR: not reached.
Figure 2.
Figure 2.
Incidence of treatment-emergent adverse events (TEAEs) over time. (A) Grade ≥3 TEAEs generally decreased over time with lower rates associated with ibrutinib use in second versus later lines. (B) Any-grade serious TEAEs generally decreased over time with lower rates associated with ibrutinib use in second versus later lines. (C) Incidence of grade ≥3 AF and bleeding was highest in year 1 and decreased thereafter. Overall population is the full ibrutinib cohort enrolled in the original three studies (N=370), including those who continued on to the CAN3001 study. Number of patients with adverse events shown on bars. Recurrent events per patient were counted only once per year. If recurrent events occurred in a single patient in separate years, these were counted separately in each year (once only per year). N: number; AF: atrial fibrillation; Yr: year.

References

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