Effect of fenretinide on ovarian carcinoma occurrence

被引:70
作者
De Palo, G
Mariani, L
Camerini, T
Marubini, E
Formelli, F
Pasini, B
Decensi, A
Veronesi, U
机构
[1] Ist Nazl Tumori, Unit Prevent Med, I-20133 Milan, Italy
[2] Ist Nazl Tumori, Canc Family Clin, I-20133 Milan, Italy
[3] Ist Nazl Tumori, Unit Med Stat & Biometry, I-20133 Milan, Italy
[4] Ist Nazl Tumori, Chemoprevent Unit, I-20133 Milan, Italy
[5] European Inst Oncol, Div Chemoprevent, Milan, Italy
关键词
ovarian carcinoma; fenretinide;
D O I
10.1006/gyno.2002.6663
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. The aim of this study was to update the effect of fenretinide, a synthetic vitamin A analogue proposed for chemo-prevention, on the occurrence of ovarian carcinoma. Methods. Data were obtained from a randomized clinical trial for the prevention of second breast cancer. For the present investigation, events of interest were new primary carcinomas of the ovary arising in the fenretinide or the no-treatment (control) arm. The probability of carrying a BRCA germ-line mutation was assessed in women with ovarian carcinoma according to G. Parmigiani et al. (1998, Am J Hum Genet 62, 145-58). Results. Fenretinide reduced ovarian carcinoma occurrence during the 5-year intervention period (0 versus 6 cases in the fenretinide and control arm, P = 0.0327). This effect was no longer evident after the 5-year intervention period (6 versus 4 cases, P = 0.7563). Therefore with median observation time of 121 months, a total of 6 carcinomas of the ovary occurred in the fenretinide group and 10 in the control group. The probability of carrying a BRCA mutation was lower for women with ovarian carcinoma in the treatment arm. Conclusion. Fenretinide treatment was associated with a lower incidence of ovarian carcinoma during the intervention period but such a protective effect seems to disappear after treatment. Furthermore, a possible protective effect of fenretinide in BRCA-mutated women was suggested. Further studies on fenretinide for the prevention of ovarian carcinoma particularly in women with genetic susceptibility appear necessary. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:24 / 27
页数:4
相关论文
共 17 条
[1]  
[Anonymous], 1986, GYNECOL ONCOL
[2]  
CHIESA F, 1993, J CELL BIOCHEM, P255
[3]  
*CYT SOFTW CORP, 1986, STATX WIND US MAN, P407
[4]   Chemoprevention trial of contralateral breast cancer with fenretinide. Rationale, design, methodology, organization, data management, statistics and accrual [J].
De Palo, G ;
Camerini, T ;
Marubini, E ;
Costa, A ;
Formelli, F ;
Del Vecchio, M ;
Mariani, L ;
Miceli, R ;
Mascotti, G ;
Magni, A ;
Campa, T ;
Di Mauro, MG ;
Attili, A ;
Maltoni, C ;
Del Turco, MR ;
Decensi, A ;
D'Aiuto, G ;
Veronesi, U .
TUMORI JOURNAL, 1997, 83 (06) :884-894
[5]   CAN FENRETINIDE PROTECT WOMEN AGAINST OVARIAN-CANCER [J].
DEPALO, G ;
VERONESI, U ;
CAMERINI, T ;
FORMELLI, F ;
MASCOTTI, G ;
BONI, C ;
FOSSER, V ;
DELVECCHIO, M ;
CAMPA, T ;
COSTA, A ;
MARUBINI, E .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (02) :146-147
[6]  
FORMELLI F, 1993, CANCER RES, V53, P5374
[7]   Effects of retinoids on cancerous phenotype and apoptosis in organotypic cultures of ovarian carcinoma [J].
Guruswamy, S ;
Lighfoot, S ;
Gold, MA ;
Hassan, R ;
Berlin, KD ;
Ivey, RT ;
Benbrook, DM .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (07) :516-525
[8]   PREVENTION OF SKIN-CANCER IN XERODERMA PIGMENTOSUM WITH THE USE OF ORAL ISOTRETINOIN [J].
KRAEMER, KH ;
DIGIOVANNA, JJ ;
MOSHELL, AN ;
TARONE, RE ;
PECK, GL .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (25) :1633-1637
[9]   Growth-inhibitory effects of the synthetic retinoid CD437 against ovarian carcinoma models in vitro and in vivo [J].
Langdon, SP ;
Rabiasz, GJ ;
Ritchie, AA ;
Reichert, U ;
Buchan, P ;
Miller, WR ;
Smyth, JF .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1998, 42 (05) :429-432
[10]   EFFECTS OF VITAMIN-A AND ITS ANALOGS (RETINOIDS) ON NORMAL AND NEOPLASTIC-CELLS [J].
LOTAN, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 605 (01) :33-91