Ductal breast carcinomas with whole chromosome gains as a particular subset of near-diploid tumors with different metastasis free survival

• Published in: Breast cancer research and treatment 2005-08, Vol.92 (3), p.279-285
• Main Authors: ELIE, Caroline, MOLIST, Romain, ASSELAIN, Bernard, DUTRILLAUX, Bernard, MULERIS, Martine
• Format: Article
• Language: English
• Subjects: Aneuploidy; Biological and medical sciences; Breast cancer; Breast Neoplasms - diagnosis; Breast Neoplasms - genetics; Breast Neoplasms - mortality; Cancer research; Cancer therapies; Carcinoma, Ductal, Breast - diagnosis; Carcinoma, Ductal, Breast - genetics; Carcinoma, Ductal, Breast - mortality; Chromosomes; Disease-Free Survival; DNA, Neoplasm - genetics; Female; France - epidemiology; Gynecology. Andrology. Obstetrics; Humans; Mammary gland diseases; Medical sciences; Middle Aged; Multivariate Analysis; Neoplasm Metastasis; Prognosis; Proportional Hazards Models; Retrospective Studies; Survival analysis; Tumors
• ISSN: 0167-6806; 1573-7217
• DOI: 10.1007/s10549-005-3379-8

We recently proposed the existence of a subtype of slightly hyperdiploid ductal breast cancers with cytogenetic alterations differing from those usually observed in the majority of these tumors. We aimed to establish whether these tumors, which represent about 50% of those with a DNA index (DI) comprised between 1.1 and 1.3, correspond to a particular clinicopathological entity. A retrospective study of 1771 patients operated for ductal carcinomas was performed. Three classes of tumors constituted according to DI were compared for the usual clinicopathological factors and clinical outcome. About 690 tumors (39%) were diploid/hypodiploid (DI < 1.1), 134 (7.6%) were hyperdiploid (1.1 < or = DI < 1.3) and 947 (53.4%) were polyploid (DI > or = 1.3). Median follow-up time was 106 months (range 1-177). Polyploid tumors were significantly associated with large tumor size, advanced clinical stage, high histological grade and S-phase fraction (SPF), positive lymph nodes and loss of steroid receptors. Hyperdiploid and diploid/hypodiploid tumors were similar for all the variables except SPF which was significantly higher in hyperdiploid tumors (p < 0.001). Overall survival was similar in hyperdiploid and diploid/hypodiploid tumors in univariate and multivariate analysis, while hyperdiploid tumors were significantly related to a poorer metastasis free survival, both in univariate (p = 0.023) and multivariate analysis (p = 0.031). Despite very close initial clinicopathological and biological characteristics, hyperdiploid tumors differed from diploid/hypodiploid tumors by a higher risk of metastasis, possibly related to their increased SPF.