DNA FLOW CYTOMETRIC ANALYSIS IN PATIENTS WITH OPERABLE NONSMALL CELL LUNG-CARCINOMA

被引:7
作者
GRANONE, P [1 ]
CARDILLO, G [1 ]
RUMI, E [1 ]
DUGO, D [1 ]
RUMI, C [1 ]
CILETTI, S [1 ]
MARGARITORA, S [1 ]
TERRIBILE, D [1 ]
PICCIOCCHI, A [1 ]
RUMI, E [1 ]
MACCHIARINI, P [1 ]
机构
[1] UNIV CATTOLICA SACRO CUORE, DEPT GEN SURG I, I-00168 ROME, ITALY
关键词
LUNG NEOPLASMS; FLOW CYTOMETRY; DNA;
D O I
10.1016/1010-7940(93)90065-J
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fresh surgical specimens of tumors from 60 patients with previously untreated non-small cell lung carcinoma (NSCLC) who underwent radical surgery between January 1991 and October 1992 were investigated by means of flow-cytometry. The nuclear DNA measurement was carried out using a Facscan (Becton, Dickinson, USA). Analysis of the DNA content was performed in all 60 patients whilst cell cycle analysis was possible in 41 cases (68.3%). Forty-two of the 60 cases (70%) were aneuploid and 18 (30%) were diploid. The overall mean value of DNA index was 1.5. Diploid NSCLC were compared with aneuploid tumors: no significant differences in age distribution, sex ratio, histology and staging were found between the two groups (P > 0.05). An S-phase proportion of more than 10% was found in 30 out of 41 patients (73.2%). Early cancer deaths were reported in four patients (6.6%): the aneuploidy rate was very close in these patients (75%) and in the remaining surviving patients (69.6%). An S-phase proportion of more than 10% was found in 100% of early cancer deaths and in 70.2% of the remaining cases; such a difference seems of some importance although it was not statistically significant (P = 0.071). In conclusion, flow-cytometry studies seem to be a useful tool in the understanding of the biological behavior of patients with NSCLC. In the present prospective report there were no significant correlations between DNA measurements and clinical outcome, however, these results suggest that a high S-phase proportion should be seen as a possible prognostic indicator. It must be emphasized, however, that a longer follow-up and a completely standardized method are required before DNA measurements can be used with confidence as a basis for clinical decision.
引用
收藏
页码:351 / 355
页数:5
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