Clinical Study

Crucial Contributions by T Lymphocytes (Effector, Regulatory, and Checkpoint Inhibitor) and Cytokines (TH1, TH2, and TH17) to a Pathological Complete Response Induced by Neoadjuvant Chemotherapy in Women with Breast Cancer

Table 10

Univariate and multivariate (logistic regression) analyses of clinicopathological parameters as predictive factors for pathological complete response to NAC(1) in LLABCs(2) ().

ParametersUnivariate analysisMultivariate analysis
OR(3)95% CI(4) valueOR95% CI value

TILs(5): high (LPBC(6)) versus low20.223.45–118.650.00111.171.41–88.490.022
Age: <50 versus ≥500.680.17–2.710.579NANANA
Tumour size: <40 mm versus ≥40 mm1.140.29–4.510.849NANANA
Tumour grade: 3 versus 1/210.42.03–53.200.0052.990.33–27.000.328
ER(7) status: negative versus positive4.670.96–22.790.0491.010.11–9.630.994
HER-2 status: positive versus negative1.950.43–8.830.386NANANA
NAC regimen: AC-TX(8) versus AC-T3.060.74–12.630.123NANANA

NAC: neoadjuvant chemotherapy; (2)LLABCs: large and locally advanced breast cancers; (3)OR: odds ratio; (4)CI: confidence interval; (5)TILs: tumour-infiltrating lymphocytes; (6)LPBC: lymphocyte-predominant breast cancer; (7)ER: oestrogen receptor; (8)AC-TX: doxorubicin, cyclophosphamide, taxotere, and Xeloda (capecitabine), respectively; statistically significant; NA: not applicable.