Table 1.
MDS Risk Group | ||||||||
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Overall | del5qMDS | Other Risk | Lower- | |||||
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N | % | N | % | N | % | |||
| ||||||||
Cohort N, % of total | 23,855 | 100.0 | 480 | 2.0 | 6355 | 26.6 | ||
Any LEN use, % of total % of cohort receiving | 753 | 100.0 | 149 | 19.8 | 182 | 24.2 | ||
LEN† | 3.2 | 31.0 | 2.9 | |||||
LEN use by MDS diagnosis period | ||||||||
2006-first half† | 143 | 3.1 | 19 | 32.2 | 21 | 3.2 | ||
2006-second half† | 144 | 3.6 | 26 | 35.1 | 32 | 3.2 | ||
2007-first half† | 165 | 3.3 | 30 | 25.9 | 46 | 3.1 | ||
2007-second half† | 109 | 3.2 | 32 | 36.0 | 32 | 2.8 | ||
2008-first half† | 123 | 3.0 | 35 | 37.6 | 33 | 2.5 | ||
LEN use only post MDS diagnosis† | 690 | 2.9 | 141 | 29.9 | 169 | 2.7 | ||
Time to LEN Initiation from MDS diagnosis (weeks)* | ||||||||
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Median† | 11.5 | 8 | 20 | |||||
Minimum | 0 | 0 | 0 | |||||
Maximum | 132 | 89 | 125 | |||||
Mean† | 23.7 | 14.8 | 27.7 | |||||
S.e. | 1.0 | 1.5 | 2.0 | |||||
Use of ESAs and DNMTi among LEN Users* | ||||||||
N | % | N | % | N | % | |||
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Any Use | ESA† | 545 | 79.0 | 105 | 74.5 | 148 | 87.6 | |
DNMTi† | 149 | 21.6 | 17 | 12.1 | 50 | 29.6 | ||
Prior to LEN initiation | ESA† | 499 | 72.3 | 91 | 64.5 | 143 | 84.6 | |
DNMTi† | 81 | 11.7 | ** | ** | ||||
Concurrent with LEN use | ESA† | 389 | 56.4 | 86 | 61.0 | 98 | 58.0 | |
DNMTi† | 30 | 4.3 | ** | ** | ||||
After LEN discontinuation | ESA | 200 | 29.0 | 36 | 25.5 | 58 | 34.3 | |
DNMTi | 76 | 11.0 | ** | ** | ||||
Duration, adherence of LEN use | ||||||||
# 28 day cycles supplied | ||||||||
Mean (s.e.) | 4.1 | 0.18 | 5.1 | 0.47 | 4.2 | 0.34 | ||
Median | 2 | 3 | 2 | |||||
Maximum | 29.8 | 29.8 | 26 | |||||
Received > 3 cycles(%) | 34.3 | 44.7 | 36.7 | |||||
Average daily dose (mg)* | ||||||||
< 3.8 | 30 | 4.3 | ** | ** | ||||
3.8 -- 4.9 | 57 | 8.3 | 17 | 12.1 | 12 | 8.5 | ||
5.0 -- 7.5 | 286 | 41.4 | 69 | 48.9 | 66 | 46.8 | ||
7.6 -- 9.9 | 43 | 6.2 | 11 | 7.8 | 13 | 9.2 | ||
10.0 -- 15.0 | 236 | 34.2 | 34 | 24.1 | 58 | 41.1 | ||
>15.0 | 38 | 5.5 | ** | ** |
Restricted to Medicare beneficiaries with continuous Part A/B/D coverage who were first dispensed lenalidomide on or after the incident MDS diagnosis in 2006-2008,first episode of lenalidomide
Suppressed due to small sample size.
Differences between del5q and other LR MDS significant at p<0.01
Abbreviations: N: number, LEN: lenalidomide; s.e.: standard error; ESA: erythropoiesis-stimulating agents; GCSF: Granulocyte colony stimulating factors, DNMTi: DNA methyltransferase inhibitors.
Source: 100% Medicare enrollment and claims for beneficiaries with MDS, enrolled in Medicare Part D, 2006-2008)