Clarke M, Coates A S, Darby S C, Davies C, Gelber R D, Godwin J, Goldhirsch A, Gray R, Peto R, Pritchard K I, Wood W C
Lancet. 2008 Jan 5;371(9606):29-40. doi: 10.1016/S0140-6736(08)60069-0.
The long-term effects of adjuvant polychemotherapy regimens in oestrogen-receptor-poor (ER-poor) breast cancer, and the extent to which these effects are modified by age or tamoxifen use, can be assessed by an updated meta-analysis of individual patient data from randomised trials.
Collaborative meta-analyses of individual patient data for about 6000 women with ER-poor breast cancer in 46 trials of polychemotherapy versus not (non-taxane-based polychemotherapy, typically about six cycles; trial start dates 1975-96, median 1984) and about 14 000 women with ER-poor breast cancer in 50 trials of tamoxifen versus not (some trials in the presence and some in the absence of polychemotherapy; trial start dates 1972-93, median 1982).
In women with ER-poor breast cancer, polychemotherapy significantly reduced recurrence, breast cancer mortality, and death from any cause, in those younger than 50 years and those aged 50-69 years at entry into trials of polychemotherapy versus not. In those aged younger than 50 years (1907 women, 15% node-positive), the 10-year risks were: recurrence 33% versus 45% (ratio of 10-year risks 0.73, 2p<0.00001), breast cancer mortality 24% versus 32% (ratio 0.73, 2p=0.0002), and death from any cause 25% versus 33% (ratio 0.75, 2p=0.0003). In women aged 50-69 years (3965 women, 58% node-positive), the 10-year risks were: recurrence 42% versus 52% (ratio 0.82, 2p<0.00001), breast cancer mortality 36% versus 42% (ratio 0.86, 2p=0.0004), and death from any cause 39% versus 45% (ratio 0.87, 2p=0.0009). Few were aged 70 years or older. Tamoxifen had little effect on recurrence or death in women who were classified in these trials as having ER-poor disease, and did not significantly modify the effects of polychemotherapy.
In women who had ER-poor breast cancer, and were either younger than 50 years or between 50 and 69 years, these older adjuvant polychemotherapy regimens were safe (ie, had little effect on mortality from causes other than breast cancer) and produced substantial and definite reductions in the 10-year risks of recurrence and death. Current and future chemotherapy regimens could well yield larger proportional reductions in breast cancer mortality.
通过对随机试验中个体患者数据进行更新的荟萃分析,可以评估辅助多药化疗方案对雌激素受体阴性(ER阴性)乳腺癌的长期影响,以及年龄或他莫昔芬的使用对这些影响的改变程度。
对46项多药化疗与非多药化疗(非紫杉烷类多药化疗,通常约6个周期;试验开始日期为1975 - 1996年,中位数为1984年)试验中约6000例ER阴性乳腺癌女性的个体患者数据进行协作荟萃分析,以及对50项他莫昔芬与非他莫昔芬治疗(部分试验联合多药化疗,部分试验未联合;试验开始日期为1972 - 1993年,中位数为1982年)试验中约14000例ER阴性乳腺癌女性的个体患者数据进行协作荟萃分析。
在ER阴性乳腺癌女性中,与未接受多药化疗相比,多药化疗显著降低了年龄小于50岁以及年龄在50 - 69岁进入多药化疗试验的患者的复发率、乳腺癌死亡率和全因死亡率。在年龄小于50岁的患者(1907例女性,15%有淋巴结转移)中,10年风险分别为:复发率33%对45%(10年风险比0.73,2p<0.00001),乳腺癌死亡率24%对32%(风险比0.73,2p = 0.0002),全因死亡率25%对33%(风险比0.75,2p = 0.0003)。在年龄50 - 69岁的患者(3965例女性,58%有淋巴结转移)中,10年风险分别为:复发率42%对52%(风险比0.82,2p<0.00001),乳腺癌死亡率36%对42%(风险比0.86,2p = 0.0004),全因死亡率39%对45%(风险比0.87,2p = 0.0009)。70岁及以上患者很少。在这些试验中被分类为ER阴性疾病的女性中,他莫昔芬对复发或死亡影响很小,且未显著改变多药化疗的效果。
在年龄小于50岁或50 - 69岁的ER阴性乳腺癌女性中,这些较老的辅助多药化疗方案是安全的(即对乳腺癌以外原因导致的死亡率影响很小),并使10年复发和死亡风险大幅且明确降低。当前和未来的化疗方案很可能在乳腺癌死亡率方面产生更大比例的降低。