Blaes Anne H, Rehman Aamer, Vock David M, Luo Xianghua, Menge Mark, Yee Douglas, Missov Emil, Duprez Daniel
Division of Hematology/Oncology/Transplantation, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.
Division of Cardiology, University of Louisville, Louisville, KY, USA.
Vasc Health Risk Manag. 2015 Nov 24;11:591-4. doi: 10.2147/VHRM.S89842. eCollection 2015.
Anthracycline chemotherapy remains an integral part of the care for curative intent chemotherapy in breast cancer and non-Hodgkin lymphoma patients. Better tools need to be identified to predict cardiac complications of anthracycline chemotherapy.
We investigated the utility of high-sensitivity cardiac troponin T (hscTnT), N-terminal pro-B-type natriuretic peptide, cardiac troponin T and I, and creatine kinase (CK)-MB in cancer patients receiving anthracycline-based chemotherapy, in order to determine whether baseline levels or changes in these biomarkers may help predict the onset of congestive heart failure.
Eighteen consecutive patients with a pathologic diagnosis of breast cancer or non-Hodgkin lymphoma were enrolled. The median dose of doxorubicin exposure was 240 mg/m(2) (range 240-400 mg/m(2)). After treatment with doxorubicin, the hscTnT increased to 19.1 pg/mL (P<0.001). CKMB and N-terminal pro-B-type natriuretic peptide levels increased to 1.1 ng/mL and 88.3 pg/mL, respectively (P=0.02). When subjects who had a decline in left ventricular ejection fraction (LVEF) by equilibrium radionuclide ventriculography were compared to those who did not have a change in LVEF, there was a suggestion that those subjects with an elevated baseline hscTnT were more likely to have a decline in LVEF (2.7 pg/mL and 0.1 pg/mL, respectively; P=0.07). Spearman correlation demonstrated that patients with higher baseline hscTnT and CKMB tended to have a greater decline in LVEF (Spearman correlation -0.54, 95% confidence interval -0.80 to -0.08 [P=0.02], and -0.49, 95% confidence interval -0.77 to -0.01 [P=0.04], respectively).
Elevations in baseline hscTnT levels are suggestive of an oncology subgroup at high risk of developing cardiac complications from their chemotherapy. Early detection by oncologists with the use of baseline biomarkers may be clinically important in designing interventions to prevent serious anthracycline-based chemotherapy complications.
蒽环类化疗仍然是乳腺癌和非霍奇金淋巴瘤患者根治性化疗护理的一个重要组成部分。需要找到更好的工具来预测蒽环类化疗的心脏并发症。
我们研究了高敏心肌肌钙蛋白T(hscTnT)、N末端B型脑钠肽前体、心肌肌钙蛋白T和I以及肌酸激酶(CK)-MB在接受蒽环类化疗的癌症患者中的效用,以确定这些生物标志物的基线水平或变化是否有助于预测充血性心力衰竭的发生。
连续纳入18例经病理诊断为乳腺癌或非霍奇金淋巴瘤的患者。阿霉素暴露的中位剂量为240mg/m²(范围240 - 400mg/m²)。阿霉素治疗后,hscTnT升高至19.1pg/mL(P<0.001)。CKMB和N末端B型脑钠肽前体水平分别升高至1.1ng/mL和88.3pg/mL(P = 0.02)。当通过平衡放射性核素心室造影术左心室射血分数(LVEF)下降的受试者与LVEF无变化的受试者进行比较时,提示基线hscTnT升高的受试者更有可能出现LVEF下降(分别为2.7pg/mL和0.1pg/mL;P = 0.07)。Spearman相关性分析表明,基线hscTnT和CKMB较高的患者LVEF下降往往更大(Spearman相关性分别为-0.54,95%置信区间-0.80至-0.08[P = 0.02],以及-0.49,95%置信区间-0.77至-0.01[P = 0.04])。
基线hscTnT水平升高提示一个肿瘤亚组在化疗后发生心脏并发症的风险较高。肿瘤学家利用基线生物标志物进行早期检测在设计预防严重蒽环类化疗并发症的干预措施中可能具有重要的临床意义。