Wright C, Cairns J, Cantwell B J, Cattan A R, Hall A G, Harris A L, Horne C H
Division of Pathology, University of Newcastle upon Tyne, UK.
Br J Cancer. 1992 Feb;65(2):271-4. doi: 10.1038/bjc.1992.54.
Sixty-eight patients with advanced breast cancer were treated with mitoxantrone and clinical responses assessed. Expression of c-erbB-2 protein and cytosolic glutathione S-transferase (GST) isoenzymes pi, alpha and mu by the primary tumours of these patients was determined immunohistochemically, and correlated with treatment response. Tumours overexpressing c-erbB-2 (n = 16, 23%) showed a lower response rate (50% vs 58%) and shorter duration of response to treatment, compared with c-erbB-2 negative tumours. These associations were not statistically significant but survival following start of treatment was significantly shorter in the c-erbB-2 positive group. For each GST isoenzyme, the response rate and duration of response of the group showing enzyme expression did not differ significantly from those with negatively staining tumours. These data do not support a role for expression of GSTs alone in resistance to mitoxantrone monotherapy in advanced breast cancer. The poorer post treatment survival of patients with c-erbB-2 positive tumours suggests they could be selected for more intensive treatment regimens.
68例晚期乳腺癌患者接受米托蒽醌治疗并评估临床反应。通过免疫组织化学方法测定这些患者原发肿瘤中c-erbB-2蛋白以及胞质谷胱甘肽S-转移酶(GST)同工酶pi、α和μ的表达,并将其与治疗反应相关联。与c-erbB-2阴性肿瘤相比,c-erbB-2过表达的肿瘤(n = 16,23%)显示出较低的反应率(50%对58%)和较短的治疗反应持续时间。这些关联无统计学意义,但c-erbB-2阳性组开始治疗后的生存期明显较短。对于每种GST同工酶,显示酶表达的组的反应率和反应持续时间与肿瘤阴性染色组相比无显著差异。这些数据不支持单独的GST表达在晚期乳腺癌对米托蒽醌单一疗法耐药中的作用。c-erbB-2阳性肿瘤患者治疗后较差的生存期表明,他们可被选择接受更强化的治疗方案。