Review Article

Neoadjuvant Chemotherapy and Targeted Therapy in Breast Cancer: Past, Present, and Future

Table 2

Randomized trials incorporating either concurrent or sequential taxane-based neoadjuvant therapy.

TrialPhase ( )TumorsTreatmentPrimary endpointOther outcomesRef.

Aberdeen trialIII (162)≥3 cm4 × CVAP → PR/CR: 4 × CVAP versus 4 × Doc; SD/PD: 4 × DocpCR 16 versus 34%; cORR 66 versus 94%, ;
BCT 48 versus 67%;
5 y-OS (78 versus 93%, );
5 y-DFS (72 versus 90%, )
[49, 50]

NSABP B-27III (2411)T1c–3 N0, T1–3 N1; (median 9 cm)4 × AC → S versus
4 × AC → 4 × Doc → S versus 4 × AC → S → 4 × Doc
DFS (arm 2 versus 1) HR 0.92 ( );
OS ( across all 3 arms = .76);
RFI (arm 2 versus 1: HR 0.83, )
LRR (arm 2/3 versus 1) HR 0.67 ( );
BCT 62 versus 64% (ns),
ORR 86 versus 91% ( );
pCR 9 versus 19% ( ),
pCR associated with better DFS (HR 0.49, ) and OS (HR 0.36, )
[1, 51, 52]

ACCOGIII (363)≥3 cm or T4d6 × AC versus
6 × ADoc
pCR 24 versus 21% ( );
cORR 61 versus 70% ( )
No difference in RFS ( );
no difference in OS ( )
[53]

Diéras et al.III (200)T2-3 N0-14 × APac versus 4 × ACpCR 16 versus 10% ( = NA)cORR 89 versus 70%;
BCT 58 versus 45%;
DFS (18 MO: 87 versus 79%);
pCR associated with better DFS (31 MO: 91 versus 70%)
[54]

Meta-analysisIV (2455)7 randomized trialsAnthracycline-based therapy ± taxanepCR better with sequential (RR 1.73, ), but not with concomitant taxanes (RR 1.04, );
BCT higher with taxanes (RR 1.11, )
No difference in DFS (RR 0.91, )[6]

CVAP: cyclophosphamide, vincristin, doxorubicin, prednisone; Doc: doxetaxel; AC: docorubicin, cyclophosphamide; Pac: paclitaxel.