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
Department of Oncology, Helsinki University Central Hospital, Finland.
Clin Cancer Res. 2002 Mar;8(3):811-6.
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.
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.
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.
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.
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。
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。
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。
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。