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. 2012 Jun 29;7(6):e39655. doi: 10.1371/journal.pone.0039655

Table 2. Risk ratio for the association between TP53 status and response to neoadjuvant chemotherapy.

Comparison Total OR* Pathological OR Total CR* Pathological CR
N RR (95%CI) p value Ph N RR (95%CI) p value Ph N RR (95%CI) p value Ph N RR (95%CI) p value Ph
All studies 26 1.20 (1.09–1.33) <0.001 0.292 15 1.37 (1.20–1.57) <0.001 0.329 15 1.33 (1.15–1.53) <0.001 0.095 12 1.45 (1.25–1.68) <0.001 0.391
Treatment
Anthracycline-based 17 1.18 (1.04–1.33) 0.010 0.298 10 1.33 (1.19–1.62) 0.005 0.109 12 1.33 (1.15–1.54) <0.001 0.031 9 1.45 (1.24–1.69) <0.001 0.175
Type of measurement
Protein 21 1.06 (0.94–1.20) 0.310 0.796 12 1.22 (1.01–1.48) 0.041 0.637 12 1.15 (0.92–1.43) 0.235 0.209 9 1.32 (1.02–1.69) 0.032 0.659
Gene 8 1.41 (1.20–1.65) <0.001 0.207 4 1.49 (1.24–1.79) <0.001 0.089 5 1.46 (1.22–1.75) <0.001 0.076 4 1.49 (1.24–1.79) <0.001 0.089

Subgroup analysis was performed when there were at least two studies in each subgroup.

N, number of studies; Ph, p value of Q-test for heterogeneity.

*

For studies using both clinical and pathological responses, we used the pathological response data, but also examined the clinical response data, and found similar results (data not shown).

#One study (Oshima et al. [15]) used both genomic sequencing and DNA microarray analysis for gene measurement; we used genomic sequencing data, but also also examined the DNA microarray data, and found similar results (data not shown).