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bcl-2、bax、bcl-xL、bag-1、fas和fasL对晚期乳腺癌化疗反应的预测价值。

The predictive value of bcl-2, bax, bcl-xL, bag-1, fas, and fasL for chemotherapy response in advanced breast cancer.

作者信息

Sjöström Johanna, Blomqvist Carl, von Boguslawski Kristina, Bengtsson Nils-Olof, Mjaaland Ingvil, Malmström Per, Ostenstadt Björn, Wist Erik, Valvere Vahur, Takayama Shinichi, Reed John C, Saksela Eero

机构信息

Department of Oncology, Helsinki University Central Hospital, Finland.

出版信息

Clin Cancer Res. 2002 Mar;8(3):811-6.

Abstract

PURPOSE

The purpose was to evaluate the utility of some bcl-2 family proteins fas and fasL as predictive indicators for chemotherapy response in advanced breast cancer.

EXPERIMENTAL DESIGN

Between October 1994 and October 1997, 283 patients with advanced breast cancer were included in a multicenter randomized study comparing docetaxel (D) to sequential methotrexate and 5-fluorouracil (MF) after anthracycline failure. The response rates (complete response + partial response) were 42 and 21% in the D and MF arms, respectively (P < 0.001). In 126 patients, histological blocks of primary tumors were available for immunohistochemical analysis of bax, bcl-2, bcl-xL, bag-1, fas and fasL.

RESULTS

Of the investigated factors, bag-1 correlated positively with bax, bcl-2, and fasL, and fasL correlated positively with fas and bax. None of these apoptosis-related factors was associated with a response to chemotherapy either in the whole patient population or in the D or MF arms. Interestingly, low bcl-2 expression was associated with shorter time to progression (P = 0.02) and shorter overall survival (OS; P = 0.001). High fasL expression showed a trend toward shorter OS. In multivariate backwards stepwise Cox analysis, in which histological grade and estrogen receptor status (ER) were also included, bcl-2 (P = 0.01) and fasL (P = 0.005) remained highly significantly associated with OS, whereas histological grade and ER lost their significance.

CONCLUSIONS

None of the investigated apoptosis-related factors of primary tumor could predict the later response to either D or MF treatment. However, fasL and bcl-2 were strong prognostic factors. Patients who had tumors with high fasL and low bcl-2 expression had the shortest OS.

摘要

目的

评估一些bcl-2家族蛋白fas和fasL作为晚期乳腺癌化疗反应预测指标的效用。

实验设计

1994年10月至1997年10月期间,283例晚期乳腺癌患者被纳入一项多中心随机研究,该研究比较了多西他赛(D)与蒽环类药物治疗失败后序贯使用甲氨蝶呤和5-氟尿嘧啶(MF)的疗效。D组和MF组的缓解率(完全缓解+部分缓解)分别为42%和21%(P<0.001)。126例患者的原发性肿瘤组织块可用于bax、bcl-2、bcl-xL、bag-1、fas和fasL的免疫组化分析。

结果

在所研究的因素中,bag-1与bax、bcl-2和fasL呈正相关,fasL与fas和bax呈正相关。在整个患者群体或D组或MF组中,这些凋亡相关因素均与化疗反应无关。有趣的是,低bcl-2表达与较短的疾病进展时间(P=0.02)和较短的总生存期(OS;P=0.001)相关。高fasL表达显示出总生存期缩短的趋势。在多变量向后逐步Cox分析中,其中还包括组织学分级和雌激素受体状态(ER),bcl-2(P=0.01)和fasL(P=0.005)仍然与总生存期高度显著相关,而组织学分级和ER失去了其显著性。

结论

原发性肿瘤中所研究的凋亡相关因素均不能预测对D或MF治疗的后期反应。然而,fasL和bcl-2是强有力的预后因素。fasL高表达且bcl-2低表达的肿瘤患者总生存期最短。

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