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This result shows that there is no evidence to suggest that the odds of response for ETV compared to LAM is moderated by the HBeAg status.
Despite adequate power to show a 9.5% change in odds of response for every one unit change in vitD level, we did not find an association between vitD level and response to NACT.
Prenotification may have an even larger effect in mailed surveys as Edwards et al.[ 8] found that the odds of response for a mailed survey were substantially higher with prenotification (OR = 1.45; 95% CI 1.29 to 1.63) than without.
For each trial identified, we used logistic regression to estimate the odds ratio for response per one page increase in the number of pages included in the questionnaire.
The odds ratio for response to letrozole versus tamoxifen was 28 (95% CI 4.5, 177; P = 0.0004).
For calculating the odds ratios for response to first follow-up questionnaires, we used logistic regression analysis.
The odds ratio for response rates was calculated for the first mail out, second reminder and last reminder.
After adjusted for various factors (gender, age at diagnosis, chemotherapy regimens), the odds ratio for response was 2.881 (P = 0.022) for those carrying at least one variant allele.
The overall odds ratio for response in TDI appeared to vary depending on indacaterol doses, and tended to increase with increasing indacaterol doses.
When the results of these trials were pooled in a random effects meta analysis the odds ratio for response with research findings was 0.92 (95% CI 0.75 to 1.11).
The odds ratio for response at 3 months among patients with p53-positive tumors was significantly (P = .043) higher as compared to those with p53-negative tumors.
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