ASH Clinical News December 2015 | Page 64

CLINICAL NEWS Literature Scan • Have undergone AHCT during first remission (p<0.001) • Be in complete remission (p=0.002) • Have received conditioning without radiation (p=0.001) • Have undergone AHCT more recently than those who did not (p=0.009) After a median follow-up of five years, the researchers found that maintenance rituximab was associated with both improved PFS (hazard ratio [HR] = 0.44; 95% CI 0.24-0.80; p=0.007) and improved OS (HR=0.46; 95% CI 0.23-0.93; p=0.03). On the safety side, grade 4 neutropenia did occur at an increased rate in the maintenance rituximab group compared with those who did not receive it: 34 percent versus 18 percent, respectively (p=0.04). “Our data encompassed a wide span of time during which additional effective therapies in MCL were introduced and may have improved OS in patients with progression of disease after AHCT,” Dr. Graf and authors noted, including proteasome inhibitors and immunomodulators, but an analysis showed no association between the time period of AHCT and the effect of maintenance rituximab on =L