P. Ellis et al., CLINICAL PROGNOSTIC AND PREDICTIVE FACTORS FOR PRIMARY CHEMOTHERAPY IN OPERABLE BREAST-CANCER, Journal of clinical oncology, 16(1), 1998, pp. 107-114
Purpose: This study aimed to identify clinical factors that are of pro
gnostic significance or that predict for subsequent treatment outcome
in patients with large operable breast cancer treated with primary che
motherapy (PCT) at our institution. Methods: One hundred eighty-five p
atients received the following regimens: CMF or MMM (76 patients), ECF
(75 patients), AC or FEC (34 patients), followed by surgery, with rad
iotherapy (RT) given to those with breast conservation. A number of co
mmon clinical variables were assessed in relation to local recurrence-
free survival (LRFS), disease-free survival (DFS), and overall surviva
l (OS). Results: Clinical responders had improved DFS (P = .009) and O
S (P = .08) compared with nonresponders. There was no association betw
een clinical or pathologic complete remission (CR) and survival. Pretr
eatment clinical axillary node positivity was a significant predictor
of worsened DFS (P = .0001), OS (P = .0001), and LRFS (P = .03). Patie
nts remaining clinically node-positive postchemotherapy had an inferio
r outcome compared with those becoming node-negative (DFS, P = .03; OS
, P = .03) but pathologic axillary node status was not shown to predic
t for survival. Twenty-nine patients in clinical CR following PCT who
electively did not have surgery and were treated with RT alone had sig
nificantly increased local recurrence rate compared with partial respo
nders having surgery and RT (P = .02). There were no differences in DF
S or OS between these groups. On multivariate analysis, clinical axill
ary node status was the only independent predictor of OS and DFS, and
LRFS. Conclusion: Pretreatment and posttreatment clinical axillary nod
e status is a major predictor of outcome following PCT. Complete clini
cal response does not define a more favorable subgroup compared with t
hose not obtaining CR. (C) 1998 by American Society of Clinical Oncolo
gy.