Cellular immunity in breast cancer patients completing taxane treatment

被引:82
作者
Carson, WE
Shapiro, CL
Crespin, TR
Thornton, LM
Andersen, BL
机构
[1] Ohio State Univ, Coll Med, Dept Surg, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[3] Ohio State Univ, Div Med Oncol, Columbus, OH 43210 USA
[4] Ohio State Univ, Coll Med, Dept Internal Med, Columbus, OH 43210 USA
[5] Ohio State Univ, Dept Psychol, Columbus, OH 43210 USA
关键词
D O I
10.1158/1078-0432.CCR-1016-03
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: A field study of postchemotherapy immune functioning relative to the use of taxanes is reported. Immune responses in breast cancer patients were analyzed as a function of whether patients received taxane as part of their adjuvant chemotherapy. Experimental Design: Immune levels of 227 stage II/III breast cancer patients were measured immediately after surgery prior to chemotherapy and again 12 months later when all chemotherapies had been completed. T-cell blastogenesis and natural killer (NK) cell lysis levels of patients receiving taxanes (n = 55) were compared with levels of patients not receiving taxanes (n = 172). Results: Regression analyses were conducted. The administration of taxane as part of combination chemotherapy predicted increased T-cell blastogenesis and NK cell cytotoxicity after the conclusion of all chemotherapies. For the Taxane group, average phytohemagglutinin-induced blastogenesis was 37% higher and NK cell cytotoxicity was 39% higher than the values for the No-Taxane group. Conclusions: Data from group comparisons with appropriate controls in a sizable clinical sample contravene traditional wisdom that taxanes suppress patients' immune cell functions. Problems in generalizing direct-contact laboratory models to the field of cancer treatment are highlighted.
引用
收藏
页码:3401 / 3409
页数:9
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