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 7
Blood(1) and tumour-infiltrating FOXP3+ and CTLA-4+ T cells (post-NAC) in women with LLABCs(2) and pathological response elicited in tumours following NAC(3).
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Blood: data previously published (Verma et al., 2013 [21]); (2)LLABCs: large and locally advanced breast cancers; (3)NAC: neoadjuvant chemotherapy; (4)average cell count per 400x high-power field; (5)AbN: absolute number (cells/mm3); (6)Mann–Whitney test; (7)GPR (good pathological response, grades 5 and 4): no residual invasive disease, >90% loss of invasive disease, respectively; (8)PPR (poor pathological response, grades 3, 2, and 1): 30–90% loss of invasive disease, <30% loss of invasive disease, and no loss of tumour cells, respectively; (9)PCR (pathological complete response, grade 5): no residual invasive disease; statistically significant. |