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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

 

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