Study ID | Study design | Study population | Mean age ± SD, age range (years) | Pre-menopausal status / total population | Tumor histological type | NAC Protocol (n = number of patients) | pCR rate | Treatment response definition |
---|---|---|---|---|---|---|---|---|
You et al. 2017 [14] | Retrospective study; Single center | 90 patients with unilateral breast cancer | 49.84 ± 10.04 years, 28 – 69 years | 50/90; pCR group: 13/25; non-pCR group: 37/65 | 72 IDC, 5 DCIS, 2 ILC and 11 tumor classification unclear | CEF (n = 5), PC (n = 20), PE (n = 2), (n = 29) and PCH (n = 39); 6 or 8 cycles | 27.78% | pCR or non-pCR; The absence of invasive carcinoma (residual DCIS allowed) by pathologic examination |
Rella et al. 2020 [15] | Retrospective study; Single center | 228 patients with unilateral breast cancer | 47.6 ± 10 years, 24 – 74 years | pCR group: 18/30; non-pCR group: 121/198 | 162 IDC, 29 ILC and 37 other invasive carcinomas | A combination of doxorubicin and cyclophosphamide (2—4 cycles) and taxanes (+ trastuzumab if HER2-positive) | 13.2% | pCR or non-pCR; The absence of residual invasive cancer cells in the breast and ipsilateral lymph nodes (DCIS may have been present) (ypT0/is, ypN0) |
Preibsch et al. 2016 [16] | Retrospective study; Single center | 73 patients with 80 biopsy-proven breast cancers | 48.5 ± 9.9 years; 26.8 – 71.2 years | NR | 71 IDC, 8 ILC and 1 invasive apocrine carcinoma | EC + docetaxel (n = 75), trastuzumab and zoledronic acid (n = 1), paclitaxel and avastin (n = 1), taxol and herceptin (n = 2) and vinorelbine and trastuzumab (n = 1) | CR (19%); PR (57%) | According to RECIST 1.1 criteria; CR (the disappearance of all target lesions was reached); PR (at least 30% decrease in the sum of the diameters of target lesions in comparison with the baseline sum diameters); SD and PD |
Onishi et al. 2021 [19] | Retrospective study; Multiple center | 882 patients with unilateral breast cancer (with breast cancer at high risk for early recurrence) | 48 ± 10 years; NR | 457/882 | NR | Paclitaxel and/or a combination of 9 experimental agents (12 cycles), followed by anthracycline-cyclophosphamide (4 cycles; + trastuzumab if HER2-positive) | 33% | pCR or non-pCR; The absence of residual invasive carcinoma in the breast and axillary lymph nodes after NAC |
Chen et al. 2015 [17] | Retrospective study; Single center | 46 patients with unilateral breast cancer | 50 ± 11 years; NR | NR | 40 IDC, 5 ILC and 1 mixed IDC and ILC | Dose-dense AC (2—4 cycles) followed by taxane regimen (After the patient received 2 cycles of AC, the oncologist determined the response and decided the next regimen) | 52% | pCR or non-pCR; The absence of malignant cancer cells |
Dong et al. 2018 [20] | Retrospective study; Single center | 51 patients with HER2-positive unilateral IDC | 46.24 ± 8.79 years; 27 – 63 years | 27/51; pCR group: 14/23; non-pCR group: 13/28 | All were HER2-positive IDC | Docetaxel, carboplatin, and trastuzumab (n = 29); doxorubicin, cyclophosphamide, docetaxel, and trastuzumab (n = 22); at least 6 or 8 cycles | 45.1% | pCR or non-pCR; No residual tumor or only DCIS |
You et al. 2018 [21] | Retrospective study; Single center | 71 patients with HER2-positive unilateral breast cancer | 47.65 ± 10.10 years; 26 – 71 years | 37/71 | 70 IDC, 1 ILC | 4 cycles of paclitaxel, carboplatin in combination, and trastuzumab | 47.89% | pCR or non-pCR; The absence of residual invasive cancer upon hematoxylin and eosin evaluation of a complete resected breast specimen and all sampled regional lymph nodes following completion of neoadjuvant systemic therapy |
Choi et al. 2015 [22] | NR | 98 patients with invasive breast carcinoma (1 patient with bilateral breast cancer) | 50 years; 29 – 81 years | NR | 76 IDC; 3 ILC; 1 invasive carcinoma with signet ring cell, 1 IMPC, 8 DCIS, 1 LCIS, and 1 sclerosing adenosis (no tumors remained in 7 cases) | AT (n = 47); AC (n = 13); C-LTZ (n = 1); C-EPRV (n = 1); C-CPV (n = 1); EP (n = 3); EC (n = 15); ET (n = 17); DP (n = 1); 4 or 6 cycles | 17.3% | pCR or non-pCR; The absence of microscopic residual tumor or invasive foci but the presence of DCIS |
Arasu et al. 2020 [23] | Prospective study; Multiple center | 88 patients with HER2-negative stage II or III breast cancer | pCR: 46.9 years; non-pCR: 48.8 years | pCR group: 20/29; non-pCR group: 35/59 | NR | Paclitaxel alone or in combination with experimental NAC agents for 12 cycles, followed by 4 cycles of AC | 33.0% | pCR or non-pCR; The absence of residual invasive cancer in the breast or lymph nodes at the time of surgery |
Oh et al. 2018 [24] | Retrospective study; Single center | 186 patients with invasive breast cancer | 45 years; 25 – 81 years | 128/186 | NR | Adriamycin with cyclophosphamide plus docetaxel (n = 126); HER2 targeted agent-based regimens (n = 22); adriamycin with cyclophosphamide (n = 20); and FEC (n = 18) | 20.4% | pCR or non-pCR; The absence of residual invasive cancer cells in the breast and ipsilateral lymph nodes (DCIS may have been present) (ypT0/is, ypN0) |
La Forgia et al. 2021 [25] | Retrospective study; Single center | 80 patients with breast cancer from stage I to stage II | 49 years; 31 – 80 years | 32/80 | NR | 4 cycles of anthracycline combined with cyclophosphamide, and only taxanes (with and without anti-HER2-positive therapy) in the following 3 months | CR (15%); PR (55%) | According to RECIST 1.1 criteria; CR (Disappearance of all target lesions; Any pathological lymph nodes must have reduction in short axis to < 10 mm); PR (At least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters); SD and PD |
Teixeira et al. 2018 [18] | Retrospect cross-sectional observational study; Dual center | 150 patients with unilateral invasive breast cancer | 45.2 years; 20 – 74 years | NR | NR | NR | NR | pCR or non-pCR; NR |
Moliere et al. 2019 [26] | Retrospective study; Single center | 102 patients with breast cancer | 49.8 years; NR | 54/102 | NR | FEC (n = 84), additional weekly taxanes (n = 51) and trastuzumab (n = 33) | 26.5% | pCR or non-pCR; The absence of residual invasive tumor in both the breast and the axillary nodes |