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).

T cell subsetsGroups ()Intratumoural
Median (range)(4)
valueStromal
Median (range)
value% blood
Median (range)
valueAbN blood
Median (range)(5)
value(6)

FOXP3+GPR ()(7)0.0 (0.0–2.4)0.0160.8 (0.4–7.4)0.2520.53 (0.25–0.90)0.001166 (35–230)0.470
PPR ()(8)2.2 (0.6–22.2)1.4 (1.0–28.4)1.18 (0.80–1.85)157 (118–168)
PCR ()(9)0.0 (0.0–0.0)<0.0011.3 (0.4–7.4)0.6350.35 (0.25–0.90)0.007173 (49–230)0.313
Non PCR ()1.8 (0.6–22.2)1.4 (0.4–28.4)1.15 (0.53–1.85)158 (35–177)

CTLA-4+GPR ()0.0 (0.0–1.2)0.1140.0 (0.0–1.2)0.2990.58 (0.10–1.71)0.2995 (2–7)0.008
PPR ()0.4 (0.0–1.2)0.4 (0.0–5.2)0.89 (0.37–1.69)7 (6–15)
PCR ()0.0 (0.0–1.0)0.1180.0 (0.0–0.2)0.1810.55 (0.10–1.25)0.2205.5 (2–7)0.181
Non PCR ()0.3 (0.0–1.2)0.3 (0.0–5.2)0.77 (0.37–1.71)6.5 (4–15)

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.