Prognostic importance of the axillary lymph node ratio in autologous transplantation for high-risk stage II/III breast cancer

被引:11
作者
Bolwell, B
Andresen, S
Pohlman, B
Sobecks, R
Goormastic, M
Rybicki, L
Bell, K
Kalaycio, M
机构
[1] Cleveland Clin Fdn, Bone Marrow Transplant Program, Dept Hematol & Med Oncol, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Transplant Ctr, Cleveland, OH 44195 USA
关键词
autologous progenitor cell transplantation; breast cancer; axillary lymph node ratio; prognostic factors;
D O I
10.1038/sj.bmt.1703004
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The role of autologous peripheral blood progenitor cell (PBPC) transplantation for high-risk stage II/III breast cancer remains controversial. New prognostic indicators defining subsets of patients who may benefit from autologous PBPC transplantation would be clinically useful. The axillary lymph node ratio, defined by the total number of axillary nodes involved with cancer divided by the number of axillary nodes surgically sampled, has been reported to be of potential prognostic importance in transplantation for high-risk, stage II/III breast cancer. We therefore retrospectively reviewed 111 women with high-risk, stage II/III breast cancer with at least four positive axillary lymph nodes undergoing autologous PBPC transplantation from 1991 to June 1999. None of the patients had received prior radiotherapy and all had completed one, and only one, course of at least three cycles of adjuvant chemotherapy. The median number of axillary nodes sampled was 20 (range 6-40) and the median number of positive axillary nodes was 12 (range 4-35). The median node ratio, dividing the number of positive nodes by the number of sampled nodes, was 0.68. Event-free survival was strongly influenced by node ratio. Patients having a node ratio of <0.7 had a 5-year event-free survival of 68%, vs those with a node ratio of <greater than or equal to>0.7 with a 5-year event-free survival of 46% (P = 0.03). Forty percent of patients with a high node ratio have relapsed vs 20% with a low node ratio (P = 0.02). Multivariate analysis revealed that positive estrogen receptor status and a node ratio of <0.7 were independent factors related to better event-free survival (P = 0.0001 and P = 0.004, respectively). We conclude that patients having a node ratio of <0.7 have a significantly better prognosis following autologous PBPC transplantation than do patients with a ratio greater than or equal to0.7.
引用
收藏
页码:843 / 846
页数:4
相关论文
共 25 条
[1]   neu/erbB-2 amplification identifies a poor-prognosis group of women with node-negative breast cancer [J].
Andrulis, IL ;
Bull, SB ;
Blackstein, ME ;
Sutherland, D ;
Mak, C ;
Sidlofsky, S ;
Pritzker, KPH ;
Hartwick, RW ;
Hanna, W ;
Lickley, L ;
Wilkinson, R ;
Qizilbash, A ;
Ambus, U ;
Lipa, M ;
Weizel, H ;
Katz, A ;
Baida, M ;
Mariz, S ;
Stoik, G ;
Dacamara, P ;
Strongitharm, D ;
Geddie, W ;
McCready, D .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) :1340-1349
[2]   High-dose chemotherapy with autologous hematopoietic stem-cell support for breast cancer in North America [J].
Antman, KH ;
Rowlings, PA ;
Vaughan, WP ;
Pelz, CJ ;
Fay, JW ;
Fields, KK ;
Freytes, CO ;
Gale, RP ;
Hillner, BE ;
Holland, HK ;
Kennedy, MJ ;
Klein, JP ;
Lazarus, HM ;
McCarthy, PL ;
Saez, R ;
Spitzer, G ;
Stadtmauer, EA ;
Williams, SF ;
Wolff, S ;
Sobocinski, KA ;
Armitage, JO ;
Horowitz, MM .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (05) :1870-1879
[3]   High-dose chemotherapy with autologous peripheral blood progenitor cell support for primary breast cancer in patients with 4-9 involved axillary lymph nodes [J].
Bearman, SI ;
Overmoyer, BA ;
Bolwell, BJ ;
Taylor, CW ;
Shpall, EJ ;
Cagnoni, PJ ;
Mechling, BE ;
Ronk, B ;
Baron, AE ;
Purdy, MH ;
Ross, M ;
Jones, RB .
BONE MARROW TRANSPLANTATION, 1997, 20 (11) :931-937
[4]  
CARTER CL, 1989, CANCER-AM CANCER SOC, V63, P181, DOI 10.1002/1097-0142(19890101)63:1<181::AID-CNCR2820630129>3.0.CO
[5]  
2-H
[6]   STAGING OF BREAST-CANCER AND SURVIVAL RATES - AN ASSESSMENT BASED ON 50 YEARS OF EXPERIENCE WITH RADICAL-MASTECTOMY [J].
FERGUSON, DJ ;
MEIER, P ;
KARRISON, T ;
DAWSON, PJ ;
STRAUS, FH ;
LOWENSTEIN, FE .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1982, 248 (11) :1337-1341
[7]  
FISHER B, 1969, CANCER, V24, P1071, DOI 10.1002/1097-0142(196911)24:5<1071::AID-CNCR2820240533>3.0.CO
[8]  
2-H
[9]  
FISHER B, 1983, CANCER-AM CANCER SOC, V52, P1551, DOI 10.1002/1097-0142(19831101)52:9<1551::AID-CNCR2820520902>3.0.CO
[10]  
2-3