
Breast cancer
NSABP-B15 trial | 1990 | TNBC perioperative |
CALGB 9344 trial | 2003 | TNBC perioperative |
CALGB 9741 trial | 2003 | TNBC perioperative |
USORTC-9735 trial | 2009 | TNBC perioperative |
CALGB 40101 trial | 2012 | TNBC perioperative |
CALGB 40603 (Alliance) trial | 2015 | TNBC perioperative |
CREATE-X trial | 2017 | TNBC perioperative |
Keynote-522 | 2020 | TNBC perioperative |
OlympiA trial | 2021 | TNBC perioperative |
NSABP-B15 trial
Fisher B et al, JCO, 1990; PMID:2202791
TNBC perioperative
Background: Women with primary operable breast cancer and at least one positive axillary node, underwent surgery and received following adjuvant treatment in 2-5 wks after the surgery.
Arm A: doxorubicin and cyclophosphamide (AC) 60/600 q 21 d for 4 cycles.
Arm B: doxorubicin and cyclophosphamide (AC) 60/600 q 21 d for 4 cycles, 6mo later received CMF 750/40/600 q 28 days for 3 cycles
Arm C: conventional (at that time) CMF for 6 cycles (Cylophosphomide:100 d1to14, q28d, Methotrexate 400d1 and d8 q28d, and 5-FU 600 d1 and d8 q28 days for 6 cycels.
mFollow up: 3yr
No significant difference in DFS (P=.5), DDFS (P=.5), or OS (P=.8) with less toxicities.
AC was completed on day 63 vs CMF on day 154, patient visit doctors 3 times less with AC, nausea control meds were given for 12 d in AC and for 84 days in CMF group.
Conclusions: This study established AC as a backbone of adjuvant chemotherapy regiment in node positive localized breast cancer.
Summarized by Veli Bakalov, MD