![]() |
![]() |
![]() |
front |1 |2 |3 |4 |5 |6 |7 |8 |9 |10 |11 |12 |13 |14 |15 |16 |17 |18 |19 |20 |21 |22 |23 |24 |25 |review |
Higher Cytogenetic Response Rates With Gleevec�* Major Cytogenetic Response� Complete Cytogenetic Response� 0 20 40 60 80 100 Gleevec IFN-α + ara-C % of Patients 0 20 40 60 80 100 Gleevec IFN-α + ara-C % of Patients 76%� 12% 54%� 3% �P<0.001. Confirmed responses shown. Unconfirmed MCR�Gleevec: 83%; IFN-α + ara-C: 20%. Unconfirmed CCR�Gleevec: 68%; IFN-α + ara-C: 7%. *IRIS Study; n=553 in each arm. �≤35% Ph+ cells. �0% Ph+ cells. For important safety information, please see slide 3 or full Prescribing Information. [Slide 15] Higher Cytogenetic Response Rates With Gleevec�1,2 � The data were analyzed using Fischer�s Exact Test. � A statistically significantly higher percentage of patients achieved a major cytogenetic response (≤35% Ph+ cells) with Gleevec (76% confirmed, 83% unconfirmed) versus IFN-α + ara-C (12% confirmed, 20% unconfirmed); P<0.001. � A statistically significantly higher percentage of patients achieved a complete cytogenetic response (0% Ph+ cells) with Gleevec (54% confirmed, 68% unconfirmed) versus IFN-α + ara-C (3% confirmed, 7% unconfirmed); P<0.001. � Confirmed responses were observed on 2 occasions ≥4 weeks apart; unconfirmed responses were observed on 1 occasion. References 1. Gleevec� (imatinib mesylate) Prescribing Information. East Hanover, NJ: Novartis Pharmaceuticals Corporation; 2003. 2. Data on file. Novartis Pharmaceuticals Corporation, East Hanover, NJ. |