Department of General Surgery, the First Medical Center of the Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Ann Palliat Med. 2021 May;10(5):5502-5508. doi: 10.21037/apm-21-533.
Recent studies have shown that chemotherapy can cause abnormal glucose and lipid metabolism in breast cancer patients; however, the effects of different chemotherapy regimens on the glucose and lipid profiles in this population remain unclear.
The clinical data of 141 invasive breast cancer patients who were treated in our center from January 2019 to December 2020 were retrospectively collected. All patients received surgical treatment and postoperative chemotherapy in our center. According to the postoperative chemotherapy regimens, these patients were divided into an observation group (n=100, treated with anthracycline-based regimens) and a control group (n=41, treated with non-anthracycline-based regimens). Blood glucose and lipid profiles were compared between the 2 groups.
Compared with the control group, the observation group had a significantly higher radiotherapy rate (74.00% vs. 43.90%, P=0.001) and a significantly higher proportion of patients receiving >6 cycles of chemotherapy (85.00% vs. 4.88%, P=0.000). There were no significant significances in the levels of total cholesterol (TC), triglyceride (TG), low-density lipoprotein (LDL) before and after treatment (P>0.05) in both groups. TC and high-density lipoprotein (HDL) were not significantly different between the observation group and control group before chemotherapy (P>0.05). After chemotherapy, fasting blood glucose significantly increased in the observation group (5.31±0.98 vs. 4.96±0.53, P=0.031), while HDL significantly decreased (1.08±0.28 vs. 1.19±0.31, P=0.042). Multivariate logistic regression analysis showed that anthracycline-based chemotherapy was a protective factor for increased fasting blood glucose after chemotherapy in invasive cancer breast patients [P=0.022, odds ratio (OR) =0.227, 95% confidence interval (CI): 0.064-0.808], whereas receiving >6 cycles of chemotherapy was a risk factor for increased fasting blood glucose (P=0.014, OR =4.216, 95% CI: 1.337-13.296).
Anthracyclines have little effect on fasting blood glucose in breast cancer patients; however, the incidence of abnormal blood glucose metabolism is gradually increasing after prolonged anthracycline use. Compared with other chemotherapy drugs, anthracycline-based chemotherapy has no significant impact on blood lipid metabolism.
最近的研究表明,化疗会导致乳腺癌患者的葡萄糖和脂质代谢异常;然而,不同化疗方案对该人群血糖和血脂谱的影响尚不清楚。
回顾性收集了 2019 年 1 月至 2020 年 12 月在我院治疗的 141 例浸润性乳腺癌患者的临床资料。所有患者均在我院接受手术治疗和术后化疗。根据术后化疗方案,将这些患者分为观察组(n=100,采用蒽环类药物治疗)和对照组(n=41,采用非蒽环类药物治疗)。比较两组患者的血糖和血脂谱。
与对照组相比,观察组的放疗率显著更高(74.00% vs. 43.90%,P=0.001),接受>6 个周期化疗的患者比例也显著更高(85.00% vs. 4.88%,P=0.000)。两组患者治疗前后的总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白(LDL)水平均无显著差异(P>0.05)。观察组化疗前 TC 和高密度脂蛋白(HDL)与对照组比较差异无统计学意义(P>0.05)。化疗后,观察组空腹血糖明显升高(5.31±0.98 vs. 4.96±0.53,P=0.031),HDL 明显降低(1.08±0.28 vs. 1.19±0.31,P=0.042)。多因素 logistic 回归分析显示,蒽环类药物化疗是浸润性乳腺癌患者化疗后空腹血糖升高的保护因素[P=0.022,比值比(OR)=0.227,95%置信区间(CI):0.064-0.808],而接受>6 个周期化疗是空腹血糖升高的危险因素(P=0.014,OR=4.216,95% CI:1.337-13.296)。
蒽环类药物对乳腺癌患者的空腹血糖影响较小;然而,在长期使用蒽环类药物后,异常血糖代谢的发生率逐渐增加。与其他化疗药物相比,蒽环类药物化疗对血脂代谢没有显著影响。