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(VCCEP) Tier 1 Pilot Submission for BENZENE - Tera

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These findings illustrate examples of studies with sufficient power that discern age-related<br />

differences, but did not find that the risk of AML was dependent on age. Currently available<br />

scientific and medical literature describing chemotherapy-induced AML in children appears to<br />

indicate that children are not more sensitive <strong>for</strong> developing AML following leukemogenic<br />

chemical exposure.<br />

PERCENT DEVELOPING t-AML<br />

8%<br />

6%<br />

4%<br />

2%<br />

0%<br />

2% (n=51)<br />

Benzene <strong>VCCEP</strong> <strong>Submission</strong><br />

March 2006<br />

6% (n=51)<br />

6% (n=51)<br />

162<br />

6% (n=51)<br />

7.5<br />

AGE (years)<br />

Figure 8.2: Percent of children who developed t-AML following treatment <strong>for</strong> ALL with<br />

etoposide (adapted from Winick et al., 1993).<br />

ABSOLUTE EXCESS RISK OF t-AML<br />

7<br />

6<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

2.6<br />

4.0<br />

6.5<br />

0–4 5–9 >10<br />

AGE (years)<br />

Figure 8.3: Age dependency of absolute excess risk of developing t-AML following treatment<br />

with alkylating agents. Adapted from Tucker et al. (1987)

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