Table 2.
Modifier | Data With Doses <0.2 Gy |
Data With Doses <0.1 Gy |
|||||
---|---|---|---|---|---|---|---|
Cases | RR0.2 Gya | θ | Cases | RR0.2Gya | θ | ||
None | 252 | 3.2 | 2.84 | 184 | 2.9 | 2.17 | |
Sex | |||||||
Male | 58 | 4.2 | 2.93 | 44 | 5.0 | 2.31 | |
Female | 194 | 3.0 | 140 | 2.4 | |||
P valueb | 0.35 | 0.15 | |||||
Age at exposure (y) | |||||||
<1 | 40 | 1.6 | 3.49 | 30 | 0.4 | 2.77 | |
1–4 | 64 | 4.2 | 31 | 2.9 | |||
5–9 | 84 | 3.9 | 71 | 3.9 | |||
10–14 | 42 | 3.5 | 35 | 3.7 | |||
15–19 | 22 | 1.6 | 17 | 0.6 | |||
P valuec | 0.01 | 0.05 | |||||
Attained age (y) | |||||||
<20 | 17 | 9.4 | 3.72 | 10 | 7.5 | 2.49 | |
20–29 | 43 | 5.5 | 25 | 4.1 | |||
30–39 | 48 | 2.6 | 33 | 2.0 | |||
40–49 | 60 | 2.2 | 48 | 2.6 | |||
50–59 | 62 | 3.1 | 52 | 3.2 | |||
60+ | 22 | 2.5 | 16 | 1.9 | |||
P valuec | 0.01 | 0.13 | |||||
Time since exposure (y) | |||||||
<20 | 37 | 5.3 | 3.16 | 22 | 4.2 | 2.41 | |
20–29 | 49 | 3.5 | 36 | 3.5 | |||
30–34 | 33 | 3.4 | 22 | 1.7 | |||
35–39 | 33 | 3.3 | 22 | 2.3 | |||
40–44 | 36 | 2.4 | 28 | 2.2 | |||
45+ | 64 | 2.3 | 54 | 3.2 | |||
P valuec | 0.02 | 0.26 | |||||
Number of treatmentsd | |||||||
1 | 226 | 3.5 | 2.80 | 170 | 3.4 | 2.13 | |
≥2 | 20 | 2.4 | 8 | 0.4 | |||
P valueb | 0.25 | 0.25 |
Pooled data limited to doses <0.2 Gy or <0.1 Gy.
Fitted RRs from a linear model in radiation dose with an additive effect for chemotherapy treatment, c, . Models adjusted for study, sex, age, and study-specific factors (see text). For modifiers, d) replaced βd where zj was an indicator variable for category j and βj was a linear parameter. There were 142 with nonexposed cases. For <0.2 Gy and <0.1 Gy, β estimates with 95% CI were 11.1 (6.6, 19.7) and 9.6 (3.7, 17.0), respectively.
Fitted RR at 0.2 Gy.
P value for likelihood ratio test of no variation based on a binary modifier.
P value for likelihood ratio test of no variation based on continuous modifier.
The definition of fractionation, which involved time between fractions, dose per fraction, and reason, varied by study. One treatment included all dose fractions received within 6 months in most studies and within 1 year for the Tinea Capitis Study.