Maintenance rituximab after autologous stem cell transplantation in patients with mantle cell lymphoma

High-dose therapy and autologous stem cell transplantation (ASCT) improves outcomes for patients with mantle cell lymphoma (MCL), but relapse ultimately occurs in most patients. Recently presented interim results from a phase III prospective trial suggest maintenance rituximab (MR) after ASCT for MC...

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Veröffentlicht in:Annals of oncology 2015-11, Vol.26 (11), p.2323-2328
Hauptverfasser: Graf, S.A., Stevenson, P.A., Holmberg, L.A., Till, B.G., Press, O.W., Chauncey, T.R., Smith, S.D., Philip, M., Orozco, J.J., Shustov, A.R., Green, D.J., Libby, E.N., Bensinger, W.I., Pagel, J.M., Maloney, D.G., Zhou, Y., Cassaday, R.D., Gopal, A.K.
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Sprache:eng
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Zusammenfassung:High-dose therapy and autologous stem cell transplantation (ASCT) improves outcomes for patients with mantle cell lymphoma (MCL), but relapse ultimately occurs in most patients. Recently presented interim results from a phase III prospective trial suggest maintenance rituximab (MR) after ASCT for MCL improves progression-free survival (PFS). The maturation of these data and any benefit of MR on overall survival (OS) remain to be defined. In this retrospective study, we examined a cohort of consecutive patients with MCL that underwent ASCT for MCL at our center and evaluated their outcomes according to whether they received MR after ASCT (n = 50) or did not (n = 107). MR was treated as a time-dependent covariate to account for variation in timing of its initiation. MR was associated with an improved PFS [hazard ratio (HR) 0.44; confidence interval (CI) (0.24–0.80), P = 0.007] and overall survival (OS; HR 0.46; CI 0.23–0.93, P = 0.03) following a multivariate adjustment for confounding factors with a median follow-up of ∼5 years. Grade 4 neutropenia was increased (34% versus 18%, P = 0.04) in the MR group, but no effect on the rate of mortality unrelated to relapse was observed. These data support that MR after ASCT for MCL confers a benefit in PFS and additionally suggest it may improve OS. General application of this strategy will require confirmation of benefit in prospective randomized trials.
ISSN:0923-7534
1569-8041
DOI:10.1093/annonc/mdv364