Adenoid cystic carcinoma of the breast - Molecular markers, treatment, and clinical outcome

被引:143
作者
Arpino, G
Clark, GM
Mohsin, S
Bardou, VJ
Elledge, RM
机构
[1] Baylor Coll Med, Breast Ctr, Houston, TX 77030 USA
[2] Inst J Paoli I Calmettes, F-13009 Marseille, France
关键词
adenoid cystic carcinoma (ACC) of the breast; breast carcinoma; adenoid cystic carcinoma; cancer; treatment; molecular marker;
D O I
10.1002/cncr.10455
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The objective of this study was to comprehensively characterize the clinical and biologic features of adenoid cystic carcinoma (ACC) and to assess the implications for management in a large cohort of patients. METHODS. From a database of 50,000 patients, 28 were identified with ACC for which clinical follow-up and biologic information was available. The biologic features examined included estrogen receptor and progesterone receptor status, DNA ploidy, and S-phase fraction. Median follow-up was 83 months with a range of 29 to 144 months. Overall survival and disease free survival curves were drawn using Kaplan and Meier estimates and were compared by the log-rank test. RESULTS. All but one patient were postmenopausal with a median age at diagnosis of 66 years (range, 40-96 years). One patient had macroscopic metastatic disease at diagnosis. Median tumor size was 1.9 cm (range, 0.5-7.0 cm). Axillary lymph node dissection was performed in 23 patients. Only I patient (4%) had histologic positive lymph nodes (2 of 10), and no recurrence was detected for this patient. Forty-six percent were ER positive (median, 16 fmol/mg protein; range, 5-1017 fmol/mg), and 35% were PgR positive (median, 61 fmol/mg protein; range, 6-854 fmol/mg). S-phase fraction and DNA ploidy were assessable in 24 cases. Ninety percent of tumors had low S-phase (median, 3.3%; range, 0.1-34.2%), and 92% were diploid. Simple or modified radical mastectomy was performed in 22 patients, and 6 patients were treated by lumpectomy. Five of these six patients also received radiation therapy after lumpectomy. Despite the different surgical approaches, there were no local recurrences. The 5-year disease free survival rate was 100%, and the 5-year overall survival rate was 85% (95% confidence interval, 71.7-98.6%). CONCLUSIONS. Adenoid cystic carcinomas of the breast have very favorable biologic characteristics and, consistent with this, an excellent prognosis. Good local control can be achieved by lumpectomy with radiation or by simple mastectomy. Axillary lymph node dissection is not helpful in clinical management. (C) 2002 American Cancer Society.
引用
收藏
页码:2119 / 2127
页数:9
相关论文
共 77 条
[1]   ADENOID CYSTIC CARCINOMA OF BREAST - PREVALENCE, DIAGNOSTIC CRITERIA, AND HISTOGENESIS [J].
ANTHONY, PP ;
JAMES, PD .
JOURNAL OF CLINICAL PATHOLOGY, 1975, 28 (08) :647-655
[2]   QUANTITATIVE GROWTH FRACTION EVALUATION WITH MIBI AND KI67 ANTIBODIES IN BREAST CARCINOMAS [J].
BARBARESCHI, M ;
GIRLANDO, S ;
MAURI, FM ;
FORTI, S ;
ECCHER, C ;
MAURI, FA ;
TOGNI, R ;
DALLAPALMA, P ;
DOGLIONI, C .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1994, 102 (02) :171-175
[3]   DNA MEASUREMENT BY IMAGE-ANALYSIS OF PARAFFIN-EMBEDDED BREAST-CARCINOMA TISSUE - A COMPARATIVE INVESTIGATION [J].
BOSARI, S ;
WILEY, BD ;
HAMILTON, WM ;
DUGAN, JM ;
COOK, LB ;
LEE, AKC .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1991, 96 (06) :698-703
[4]  
CAMMOUN H, 1972, Annales d'Anatomie Pathologique, V17, P143
[5]  
CAVANZO FJ, 1969, CANCER, V24, P740, DOI 10.1002/1097-0142(196910)24:4<740::AID-CNCR2820240412>3.0.CO
[6]  
2-H
[7]  
CLARK GM, 1993, CANCER-AM CANCER SOC, V71, P2157, DOI 10.1002/1097-0142(19930315)71:6+<2157::AID-CNCR2820711606>3.0.CO
[8]  
2-O
[9]   PREDICTION OF RELAPSE OR SURVIVAL IN PATIENTS WITH NODE-NEGATIVE BREAST-CANCER BY DNA FLOW-CYTOMETRY [J].
CLARK, GM ;
DRESSLER, LG ;
OWENS, MA ;
POUNDS, G ;
OLDAKER, T ;
MCGUIRE, WL .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (10) :627-633
[10]   PLEOMORPHIC ADENOMA .1. ULTRASTRUCTURAL ORGANIZATION OF EPITHELIAL REGIONS [J].
DARDICK, I ;
VANNOSTRAND, AWP ;
JEANS, MTD ;
RIPPSTEIN, P ;
EDWARDS, V .
HUMAN PATHOLOGY, 1983, 14 (09) :780-797