Leucocyte nadir as a marker for chemotherapy efficacy in node-positive breast cancer treated with adjuvant CMF

被引:95
作者
Poikonen, P
Saarto, T
Lundin, J
Joensuu, H
Blomqvist, C
机构
[1] Univ Helsinki, Cent Hosp, Dept Oncol, FIN-00029 Helsinki, Finland
[2] HUCH Clin Res Inst, Helsinki, Finland
关键词
adjuvant chemotherapy; breast neoplasms; CMF; leucopenia;
D O I
10.1038/sj.bjc.6690594
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to examine the association between the leucocyte nadir and prognosis in breast cancer patients receiving adjuvant chemotherapy consisting of cyclophosphamide, methotrexate and fluorouracil (CMF). Three hundred and sixty-eight patients with node-positive breast cancer without distant metastases were treated with six cycles of adjuvant CMF. Some patients (n = 60) also received tamoxifen. All patients underwent surgery and received radiotherapy to the axillary and supraclavicular lymph nodes and the chest wall. The effect of leucopenia caused by CMF on distant disease-free survival (DDFS) and overall survival (OS) was assessed. A low leucocyte nadir during the chemotherapy was associated with a long DDFS in univariate analysis when tested as a continuous variable (the relative risk (RR) 1.3, 95% confidence interval (CI) 1.04-1.06, P = 0.02). Similarly, when the leucocyte nadir count was divided into tertiles, the patients who had the highest nadir values during the six-cycle treatment had worst outcome (RR 1.6, 95% CI 1.07-2.5, P = 0.02). However, in a multivariate analysis only the number of affected lymph nodes, tumour size, progesterone receptor status, surgical procedure, age and adjuvant tamoxifen therapy retained prognostic significance, whereas the leucocyte nadir count did not. A low leucocyte nadir during the adjuvant CMF chemotherapy is associated with favourable DDFS and it may be a useful biological marker for chemotherapy efficacy.
引用
收藏
页码:1763 / 1766
页数:4
相关论文
共 24 条
[1]   A PRELIMINARY ASSESSMENT OF FACTORS ASSOCIATED WITH RECURRENT DISEASE IN A SURGICAL ADJUVANT CLINICAL-TRIAL FOR PATIENTS WITH BREAST-CANCER WITH SPECIAL EMPHASIS ON THE AGGRESSIVENESS OF THERAPY [J].
AHMANN, DL ;
OFALLON, JR ;
SCANLON, PW ;
PAYNE, WS ;
BISEL, HF ;
EDMONSON, JH ;
FRYTAK, S ;
HAHN, RG ;
INGLE, JN ;
RUBIN, J ;
CREAGAN, ET .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1982, 5 (04) :371-381
[2]   ANALYSIS OF DOSE INTENSITY IN DOXORUBICIN-CONTAINING ADJUVANT CHEMOTHERAPY IN STAGE-II AND STAGE-III BREAST-CARCINOMA [J].
ANG, PT ;
BUZDAR, AU ;
SMITH, TL ;
KAU, S ;
HORTOBAGYI, GN .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (11) :1677-1684
[3]   DOSE-RESPONSE EFFECT OF ADJUVANT CHEMOTHERAPY IN BREAST-CANCER [J].
BONADONNA, G ;
VALAGUSSA, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (01) :10-15
[4]   Dose-response effect of adjuvant cyclophosphamide, methotrexate, 5-fluorouracil (CMF) in node-positive breast cancer [J].
Colleoni, M ;
Price, K ;
Castiglione-Gertsch, M ;
Goldhirsch, A ;
Coates, A ;
Lindtner, J ;
Collins, J ;
Gelber, RD ;
Thürlimann, B ;
Rudenstam, CM .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (11) :1693-1700
[5]  
COX DR, 1972, J R STAT SOC B, V34, P187
[6]  
*EARL BREAST CANC, 1992, LANCET, V339, P1
[7]   Increased intensification and total dose of cyclophosphamide in a doxorubicin-cyclophosphamide regimen for the treatment of primary breast cancer: Findings from National Surgical Adjuvant Breast and Bowel Project B-22 [J].
Fisher, B ;
Anderson, S ;
Wickerham, DL ;
DeCillis, A ;
Dimitrov, N ;
Mamounas, E ;
Wolmark, N ;
Pugh, R ;
Atkins, JN ;
Meyers, FJ ;
Abramson, N ;
Wolter, J ;
Bornstein, RS ;
Levy, L ;
Romond, EH ;
Caggiano, V ;
Grimaldi, M ;
Jochimsen, P ;
Deckers, P .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (05) :1858-1869
[8]  
FUMOLEAU P, 1993, DRUGS, V2, P38
[9]  
GLUCKSBERG H, 1982, CANCER, V50, P423, DOI 10.1002/1097-0142(19820801)50:3<423::AID-CNCR2820500307>3.0.CO
[10]  
2-O