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急性白血病预处理方案及造血细胞移植期间心脏毒性的生化标志物与评估

Biochemical markers and assessment of cardiotoxicity during preparative regimen and hematopoietic cell transplantation in acute leukemia.

作者信息

Horacek J M, Pudil R, Tichy M, Jebavy L, Zak P, Slovacek L, Maly J

机构信息

2nd Department of Medicine--Clinical Hematology, University Hospital and Charles University, Faculty of Medicine in Hradec Kralove, Czech Republic.

出版信息

Exp Oncol. 2007 Sep;29(3):243-7.

Abstract

INTRODUCTION

Cardiotoxicity is a relatively frequent and potentially serious complication of antitumor treatment. Anthracyclines and other high-dose chemotherapy represent the greatest risk. The aim of the study was to assess cardiotoxicity during preparative regimen (PR) and hematopoietic cell transplantation (HCT) in acute leukemia (AL) with biochemical markers - "N-terminal pro brain natriuretic peptide" (NT-proBNP), cardiac troponin T (cTnT) and creatine kinase MB (CK-MB mass).

METHODS

Nineteen adult AL patients previously treated with anthracyclines--idarubicine, daunorubicine, mitoxantrone with standard doses for a cycle as 3 x 12 mg/m(2), 3 x 50 mg/m(2), 3 x 10 mg/m(2) accordingly were studied. PR consisted of high-dose cyclophosphamide (HD-C) in combination with busulphan or total body irradiation (TBI). Plasma NT-proBNP, cTnT and CK-MB mass concentrations were measured the day before PR, the day after PR, the day after HCT and 14 days after HCT.

RESULTS

Before PR, mean plasma NT-proBNP value was 106.3+/-55.7 ng/l. After PR, it increased to 426.1+/-391.5 ng/l. After HCT, a further increase to 847.6+/-780.6 ng/l was observed. Fourteen days after HCT, the mean NT-proBNP was 330.8+/-236.8 ng/l. The differences were statistically significant in comparison with the baseline values (p<0.01). The NT-proBNP elevations were more pronounced in patients with cumulative doses (CD) of anthracyclines above 450 mg/m(2) (p<0.05), in patients with PR containing HD-C and TBI (p<0.05). In all patients, plasma cTnT and CK-MB mass concentrations remained unchangable during PR and HCT.

CONCLUSION

Our results suggest that administration of PR and HCT is in most AL patients associated with acute neurohumoral activation (significant rise in NT-proBNP). Persistent NT-proBNP elevations, in our study in 12 (63.2%) patients, indicate subclinical cardiotoxicity (risk for development of heart failure) and require further follow-up. More pronounced NT-proBNP elevations in patients with higher CD of anthracyclines and in patients with PR containing combination of HD-C and TBI confirm that these therapeutic procedures seem to be more cardiotoxic and not very appropriate for patients with cumulation of risk factors for cardiotoxicity. Negative plasma cTnT and CK-MB mass concentrations show no detectable damage of cardiomyocyte structure during PR and HCT.

摘要

引言

心脏毒性是抗肿瘤治疗中较为常见且潜在严重的并发症。蒽环类药物和其他高剂量化疗带来的风险最大。本研究旨在通过生化标志物——“N末端脑钠肽前体”(NT-proBNP)、心肌肌钙蛋白T(cTnT)和肌酸激酶同工酶MB(CK-MB质量)评估急性白血病(AL)患者在预处理方案(PR)和造血细胞移植(HCT)期间的心脏毒性。

方法

研究了19例先前接受过蒽环类药物(伊达比星、柔红霉素、米托蒽醌)治疗的成年AL患者,其标准剂量分别为每周期3×12mg/m²、3×50mg/m²、3×10mg/m²。PR包括高剂量环磷酰胺(HD-C)联合白消安或全身照射(TBI)。在PR前一天、PR后一天、HCT后一天和HCT后14天测量血浆NT-proBNP、cTnT和CK-MB质量浓度。

结果

PR前,血浆NT-proBNP平均水平为106.3±55.7ng/l。PR后,升至426.1±391.5ng/l。HCT后,进一步升至847.6±780.6ng/l。HCT后14天,NT-proBNP平均水平为330.8±236.8ng/l。与基线值相比,差异具有统计学意义(p<0.01)。蒽环类药物累积剂量(CD)高于450mg/m²的患者(p<0.05)以及接受含HD-C和TBI的PR的患者(p<0.05)中,NT-proBNP升高更为明显。在所有患者中,PR和HCT期间血浆cTnT和CK-MB质量浓度保持不变。

结论

我们的结果表明,大多数AL患者进行PR和HCT与急性神经体液激活(NT-proBNP显著升高)相关。在我们的研究中,12例(63.2%)患者NT-proBNP持续升高,表明存在亚临床心脏毒性(发生心力衰竭的风险),需要进一步随访。蒽环类药物CD较高的患者以及接受含HD-C和TBI联合治疗的PR的患者中,NT-proBNP升高更为明显,这证实这些治疗程序似乎心脏毒性更大,对存在心脏毒性危险因素累积的患者不太合适。血浆cTnT和CK-MB质量浓度阴性表明PR和HCT期间未检测到心肌细胞结构损伤。

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