Hug V, Polyzos A, Tucker S, Thames H
Department of Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston.
Br J Cancer. 1993 Feb;67(2):222-5. doi: 10.1038/bjc.1993.43.
We measured the clonogenic growth of 110 breast cancer samples obtained from 107 patients with advanced disease. We determined clonogenicity under conventional conditions and under conditions supplemented with growth factors and hormones that target breast tissue. After a median follow-up period of 6 years we analyzed our data to determine if and to what degree clonogenic growth of metastatic breast tumours was related to the survival of patients. We found that tumour clonogenicity and patient survival correlated weakly, particularly if compared to the strong correlations of patient survival with either performance status or tumour bulk. Furthermore, an association between tumour clonogenicity and patient survival was visible only for clonogenicity that was determined under hormone-supplemented conditions, and only for tumour lesions that formed 50 or more colonies per 500,000 cells cultured. Thus, we conclude that clonogenic growth of breast tumour samples incompletely reflects the tumour features that determine the course of advanced disease.
我们测量了从107例晚期疾病患者身上获取的110份乳腺癌样本的克隆形成生长情况。我们在常规条件下以及在补充了针对乳腺组织的生长因子和激素的条件下测定克隆形成能力。经过6年的中位随访期后,我们分析数据以确定转移性乳腺肿瘤的克隆形成生长是否以及在何种程度上与患者的生存相关。我们发现肿瘤克隆形成能力与患者生存之间的相关性较弱,尤其是与患者生存与体能状态或肿瘤大小之间的强相关性相比。此外,肿瘤克隆形成能力与患者生存之间的关联仅在激素补充条件下测定的克隆形成能力中可见,并且仅对于每500,000个培养细胞形成50个或更多集落的肿瘤病变可见。因此,我们得出结论,乳腺肿瘤样本的克隆形成生长不能完全反映决定晚期疾病进程的肿瘤特征。