Abstract
Background: Regular transfusion dependence is seen in almost every MDS patient (pt) during the natural course of disease. Due to deleterious sequelae of chronic transfusions, including iron-overload, alloimmunization, and infections, delaying transfusion dependence or attainment of transfusion-independence are important MDS treatment goals. The role of epoetin alfa (EPO) is well established for anemia treatment prior to transfusion dependence, although its utility in transfusion-dependent pts is not well understood. The present meta-analysis was conducted to assess the efficacy of EPO in achieving transfusion independence in transfusion-dependent MDS pts.
Methods: Data was extracted from studies from PubMed, ASCO and ASH proceedings from 1990–2006 in transfusion-dependent MDS pts treated with EPO±G/GM-CSF. Studies using International Working Group (IWG) response and IWG-like criteria with EPO±G/GM-CSF were compared with EPO monotherapy studies not using IWG criteria (Non-IWG). Pooled estimates of erythroid response (ER) rates were calculated using random-effects models. Where only pre-therapy values were available, values for post-therapy reductions in RBC requirements (units/month) were imputed based on response criteria stated in the study.
Results: Included were 578 evaluable transfusion-dependent pts representing 58% of the total study population in 25 studies. All studies collectively showed significant treatment effects from baseline (BL) as evidenced by a mean overall ER rate of 34.5% and a mean proportion of pts achieving complete transfusion independence of 23.3% with EPO±G/GM-CSF (p<.001 for both). A significant decrease was observed in mean RBC units/month after treatment (2.55 pre-therapy vs 1.96 post-therapy,p=.0002,n=17 studies). IWG studies showed numerically higher ER rates and lower transfusion requirements than Non-IWG studies (Table) (p>.05). Among IWG studies, EPO monotherapy as compared to EPO±G/GM-CSF, showed comparable ER rates (41.6% vs 36.4%,p=.643), a comparable proportion of pts achieving transfusion-independence (28.8% vs 24.8%,p=0.705), and a greater reduction in RBC units/month (34.3% vs 10.4%,p=0.339). Additionally, EPO monotherapy IWG studies showed dose response with significantly higher overall ER rates in pts receiving 60-80,000 units/week vs 30-40,000 units/week (45.3% vs 30.8%,p=.041). Multivariate regression did not yield significant association of any BL study characteristics with overall ER rate.
Conclusion: Findings from this meta-analysis showed EPO±G/GM-CSF treatment is effective in reducing transfusion requirements in transfusion-dependent MDS pts. Identification of predictors of EPO response in this population may offer significant clinical benefit to this subset.
Study Group . | Non-IWG Studies . | IWG Studies . | IWG Studies . |
---|---|---|---|
EPOMonotherapy | EPOMonotherapy | EPO +G/GM-CSF | |
No. of studies (evaluable pts) | 12(268) | 7(195) | 6(115) |
BL sEPO levels, mU/mL (Mean±SD) | 687.2±684.7 | 374.3±72.2 | 288±172.1 |
BL Hb, g/dL (Mean±SD) | 8.5±0.6 | 7.9±0.4 | 8.1±0.4 |
Initial weekly dose of EPO, Units (Mean±SD) | 48,310±41,345 | 49,326±22,752 | 34,789±12,083 |
Mean monthly pre-therapy RBC Units | 2.71 | 2.37 | 2.33 |
Pooled ER rate, % (95%CI) | 27.8(20.4–35.2) | 41.6(24.5–58.6) | 36.4(22.5–50.2) |
Post-therapy transfusion-independent pts, % (95%CI) | 17.9(10.9–24.9) | 28.8(12.6–45.1) | 24.8(11.8–37.8) |
Mean post-therapy reduction in RBC units/month, % (Median) | 17.3(17.1) | 34.3(24.7) | 10.4(11.5) |
Study Group . | Non-IWG Studies . | IWG Studies . | IWG Studies . |
---|---|---|---|
EPOMonotherapy | EPOMonotherapy | EPO +G/GM-CSF | |
No. of studies (evaluable pts) | 12(268) | 7(195) | 6(115) |
BL sEPO levels, mU/mL (Mean±SD) | 687.2±684.7 | 374.3±72.2 | 288±172.1 |
BL Hb, g/dL (Mean±SD) | 8.5±0.6 | 7.9±0.4 | 8.1±0.4 |
Initial weekly dose of EPO, Units (Mean±SD) | 48,310±41,345 | 49,326±22,752 | 34,789±12,083 |
Mean monthly pre-therapy RBC Units | 2.71 | 2.37 | 2.33 |
Pooled ER rate, % (95%CI) | 27.8(20.4–35.2) | 41.6(24.5–58.6) | 36.4(22.5–50.2) |
Post-therapy transfusion-independent pts, % (95%CI) | 17.9(10.9–24.9) | 28.8(12.6–45.1) | 24.8(11.8–37.8) |
Mean post-therapy reduction in RBC units/month, % (Median) | 17.3(17.1) | 34.3(24.7) | 10.4(11.5) |
Author notes
Disclosure:Employment: Drs Mundle, Yektashenas, and Moyo are employees of Ortho Biotech Clinical Affairs, LLC. Consultancy: Mr. Vekeman, Mr. Lefebvre, Mr. Laliberté, and Dr. Duh are paid consultants of Ortho Biotech Clincal Affairs, LLC. Ownership Interests:; Drs Mundle, Yektashenas, and Moyo own stock in Johnson & Johnson. Off Label Use: This abstract discusses a meta-analysis conducted on the use of epoetin alfa in treatment of MDS-associated anemia which is not currently an FDA-approved indication of epoetin alfa.
This feature is available to Subscribers Only
Sign In or Create an Account Close Modal