Holdaway Ian M, Mason Barbara H, Lethaby Anne E, Singh Vijay, Harvey Vernon J, Thompson Paul I, Evans Barrie D
Departments of Endocrinology and Oncology, Auckland Hospital, Auckland, New Zealand.
ANZ J Surg. 2003 Nov;73(11):905-8. doi: 10.1046/j.1445-2197.2003.02817.x.
Insulin-like growth factor-I (IGF-I) and IGF binding protein-3 (IGFBP-3) appear to influence the growth of breast cancer cells in vitro, and epidemiological studies suggest higher serum IGF-I levels increase the risk of breast cancer. IGF-I and IGFBP-3 have therefore been measured in women with advanced breast cancer to determine if changes in serum levels predict the response to treatment by chemotherapy.
Serum IGF-I and IGFBP-3 levels were measured in 14 patients before and after 1 week of chemotherapy. Changes in serum levels were compared with duration of survival.
Mean basal serum levels of IGF-I and IGFBP-3 were not significantly different between patients with advanced breast cancer and controls or women with early breast cancer. Serum IGFBP-3 fell significantly 1 week after initiation of chemotherapy. Patient survival was not significantly related to baseline IGF-I or IGFBP-3 levels, but when the fall in serum levels 1 week after starting treatment was expressed either as absolute change or as a percentage of baseline, those individuals with a decrease in IGFBP-3 greater than the median had significantly poorer survival (median survival 5.5 months vs 18 months). These results were independent of other prognostic variables such as previous disease-free survival, and were also unaffected by the change in serum albumin with treatment. The fall in IGF-I and IGFBP-3 with chemotherapy mainly occurred in those with hepatic metastases, but prediction of survival was explained solely by the extent of the fall in IGFBP-3.
This preliminary study has shown that serum IGFBP-3 falls significantly following initiation of chemotherapy and the extent of reduction significantly predicts the response to treatment.
胰岛素样生长因子-I(IGF-I)和IGF结合蛋白-3(IGFBP-3)在体外似乎会影响乳腺癌细胞的生长,并且流行病学研究表明血清IGF-I水平升高会增加患乳腺癌的风险。因此,已对晚期乳腺癌女性患者的IGF-I和IGFBP-3进行了检测,以确定血清水平的变化是否能预测化疗的治疗反应。
在14例患者化疗1周前后检测血清IGF-I和IGFBP-3水平。将血清水平的变化与生存时间进行比较。
晚期乳腺癌患者与对照组或早期乳腺癌女性患者之间,IGF-I和IGFBP-3的平均基础血清水平无显著差异。化疗开始1周后,血清IGFBP-3显著下降。患者生存与基线IGF-I或IGFBP-3水平无显著相关性,但当将治疗1周后血清水平的下降以绝对变化或基线百分比表示时,IGFBP-3下降大于中位数的个体生存明显较差(中位生存期5.5个月对18个月)。这些结果独立于其他预后变量,如既往无病生存期,并且也不受治疗后血清白蛋白变化的影响。化疗后IGF-I和IGFBP-3的下降主要发生在有肝转移的患者中,但生存预测仅由IGFBP-3的下降程度来解释。
这项初步研究表明,化疗开始后血清IGFBP-3显著下降,且下降程度能显著预测治疗反应。