Cell proliferation as a predictor of response to chemotherapy in metastatic breast cancer: A prospective study

被引:58
作者
Amadori, D
Volpi, A
Maltoni, R
Nanni, O
Amaducci, L
Amadori, A
Giunchi, DC
Vio, A
Saragoni, A
Silvestrini, R
机构
[1] IST ONCOL ROMAGNOLO, FORLI, ITALY
[2] UNIV BOLOGNA, DEPT OBSTET & GYNECOL, REPROD MED UNIT, I-40138 BOLOGNA, ITALY
[3] MORGAGNI HOSP, DEPT GEN SURG, FORLI, ITALY
[4] PIERANTONI HOSP, DEPT PATHOL, FORLI, ITALY
[5] IST NAZL STUDIO & CURA TUMORI, DEPT EXPT ONCOL C, I-20133 MILAN, ITALY
关键词
cell proliferation; chemotherapy; metastatic breast cancer; predictive value;
D O I
10.1023/A:1005780107879
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Many biologic prognostic markers are available for patients with breast cancer, and considerable interest has been devoted to confirm preliminary evidence of their role as indicators of treatment response. It remains to be assessed whether such markers are predictors of response only to first-line or also to successive therapies. Proliferative activity, defined by the H-3-thymidine labeling index (TLI), was determined on the primary lesion from 76 patients at time of first diagnosis. At relapse, patients underwent chemotherapy as absolute (48 cases) or relative (28 cases) first-line treatment, and their clinical response was analyzed in relation to the TLI of the primary lesion. The objective clinical response was significantly higher for rapidly (47%; CL, 33-61%) than for slowly proliferating tumors (15%; CL, 1-29%). These findings held true also when adjusted for metastatic site, previous treatment, chemotherapy regimen administered, and hormone receptor status. However, the direct relation between cell proliferation and benefit from chemotherapy held true only when such a treatment was used as an absolute first-line approach. Cell proliferation of primary lesions represents a consistent indicator of response to chemotherapy over time. Previously administered regimens, at least hormone therapy, could alter the proliferation-related chemosensitivity profile of individual tumors.
引用
收藏
页码:7 / 14
页数:8
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