Optimal sequence of anthracyclines and taxanes as adjuvant breast cancer treatment

被引:0
|
作者
Vici, P. [1 ]
Viola, G.
Rossi, S. [2 ]
Botti, C.
Vitucci, C.
Sergi, D.
Ferranti, F. R.
Saracca, E.
Di Lauro, L.
Corsetti, S.
Foggi, P.
Fattoruso, S. I. S.
Lopez, M.
机构
[1] Ist Nazl Tumori Regina Elena, Div Oncol Med B, I-00144 Rome, Italy
[2] Dipartimento Med Sanofi Aventis, Milan, Italy
来源
CLINICA TERAPEUTICA | 2008年 / 159卷 / 06期
关键词
adjuvant treatment; anthracyclines; sequence; taxanes;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Results from randomized trials evaluating taxane versus non-taxane containing regimens in adjuvant breast cancer treatment indicate an advantage in DFS and OS for the taxane-arms, but the best schedule of administration, in combination with anthracyclines or in sequence, is still a debated issue, even if the sequential strategy appears to be less toxic. Up to now, the majority of clinical trials employed the "standard" sequence, with anthracycline-based combinations first, followed by taxanes. Few small phase 11 trials evaluated the reverse sequence, with taxanes administered first, most of them in metastatic or neoadjuvant setting, suggesting efficacy and lower toxicity. An important issue to be considered is the hypothesized differences in the ability of the drugs to induce cross-resistance to each other, as suggested by data of a preclinical study, and from clinical study with a cross-over design; results of these trials suggest that the best strategy would be to administer a taxane prior to an anthracycline, also according to the Norton and Simon hypothesis. Moreover, trials evaluating the best sequence of anthracyclines and taxanes in adjuvant breast cancer setting are of small sample size, and an adequately powered randomized phase III trial is needed before definitive conclusions are reached. Clin Ter 2008; 159(6):453-456
引用
收藏
页码:453 / 456
页数:4
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