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. 2020 Aug 4;10:13078. doi: 10.1038/s41598-020-69965-1

Table 2.

Odds ratios (ORs) and 95% confidential intervals (CIs) for pCR in all patients.

Univariate Multivariate
OR (95% CIs) P-value OR (95% CIs) P-value
Age 0.996 (0.982–1.011) 0.62 0.992 (0.977–1.008) 0.336
NLR
< 2.74 Ref Ref
≥ 2.74 0.680 (0.476–0.971) 0.034 0.595 (0.398–0.890) 0.011
cT stage 0.002 < 0.001
1 Ref Ref
2 1.320 (0.856–2.036) 0.209 0.804 (0.489–1.324) 0.392
3 0.596 (0.336–1.056) 0.076 0.327 (0.172–0.621) 0.001
cN stage
Negative Ref Ref
Positive 0.407 (0.285–0.582) < 0.001 0.583 (0.385–0.883) 0.011
ER
Positive Ref Ref
Negative 7.713 (5.462–10.892) < 0.001 5.017 (3.033–8.299) < 0.001
PR
Positive Ref Ref
Negative 7.515 (5.034–11.220) < 0.001 2.283 (1.289–4.044) 0.005
Regimen 0.002 < 0.001
AC-T Ref Ref
AC 0.516 (0.198–1.345) 0.176 0.407 (0.142–1.168) 0.095
AT 0.381 (0.225–0.644) < 0.001 0.308 (0.174–0.544) < 0.001
Others* 0.941 (0.457–1.939) 0.870 0.741 (0.333–1.651) 0.463

pCR pathologic complete response, NLR neutrophil to lymphocyte ratio, cT clinical T stage, cN clinical N stage, ER estrogen receptor, PR progesterone receptor, AC-T doxorubicin and cyclophosphamide followed by taxane, AC doxorubicin and cyclophosphamide, AT doxorubicin and taxane.

*Others: cyclophosphamide, doxorubicin, 5-fluorouracil (CAF); cyclophosphamide, methotrexate, 5-fluorouracil (CMF); taxane; taxane plus carboplatin.