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阿霉素心脏毒性:1273例患者的调查

Adriamycin cardiotoxicity: a survey of 1273 patients.

作者信息

Praga C, Beretta G, Vigo P L, Lenaz G R, Pollini C, Bonadonna G, Canetta R, Castellani R, Villa E, Gallagher C G, von Melchner H, Hayat M, Ribaud P, De Wasch G, Mattsson W, Heinz R, Waldner R, Kolaric K, Buehner R, Ten Bokkel-Huyninck W, Perevodchikova N I, Manziuk L A, Senn H J, Mayr A C

出版信息

Cancer Treat Rep. 1979 May;63(5):827-34.

PMID:455324
Abstract

Valuable information was collected on the medical history and clinical course of 1273 patients entered in clinical trials with Adriamycin (ADR) carried out in 12 European cancer centers. A coded patient form was used for the data collection carried out in each center by a qualified physician following a guideline which was discussed and accepted by all of the participants. The aim of the study was to define the incidence, characteristics, and possible co-factors of the cardiomyopathy (CMP) in patients treated with combination chemotherapy regimens including ADR. The mean total dose of ADR was 268 mg/m2 (range, 15--1251 mg/m2), and 5.1% of the patients received a total dose of greater than 550 mg/m2. A "definite" ADR-related CMP was observed in 1.7% of the cases; another 3% of the cases were reported as "possible" ADR-CMP since the role played by the drug could not be clearly defined. "Definite" ADR-CMP was fatal in eight patients (0.6%) while "possible" ADR-CMP was fatal in 13 patients (1.0%). Among the possible co-factors examined, the following ones were found to be significantly associated with the occurrence of a "definite" ADR-CMP: (a) total dose of ADR; (b) vincristine when given both before and concomitantly with ADR; (c) bleomycin when given before ADR; and (d) radiotherapy to the mediastinum when given concomitantly with ADR. Furthermore, none of 182 patients receiving ADR by slow infusion developed a "definite" ADR-CMP, while 2% of the patients treated by bolus injection did so. The occurrence of a "possible" ADR-CMP was found to be significantly associated with two pre-existing pathologic conditions (electrocardiogram [ECG] abnormalities and hypertension) but not with the treatment-related co-factors for the "definite" ADR-CMP mentioned above. Other variables examined, such as sex, age, cancer type, baseline liver function, and cyclophosphamide treatment, did not seem to influence the risk of ADR-CMP. Data on ECG changes occurring during ADR treatment were also reported and their incidence was found to be strictly related to the frequency of the ECG monitoring.

摘要

收集了在12个欧洲癌症中心进行的阿霉素(ADR)临床试验中1273例患者的病史和临床病程的重要信息。在每个中心,由一名合格的医生按照所有参与者讨论并认可的指南,使用编码患者表格进行数据收集。该研究的目的是确定接受包括ADR在内的联合化疗方案治疗的患者中,心肌病(CMP)的发生率、特征和可能的协同因素。ADR的平均总剂量为268mg/m²(范围为15 - 1251mg/m²),5.1%的患者接受的总剂量大于550mg/m²。在1.7%的病例中观察到“明确的”与ADR相关的CMP;另有3%的病例被报告为“可能的”ADR - CMP,因为药物所起的作用无法明确界定。“明确的”ADR - CMP导致8例患者死亡(0.6%),而“可能的”ADR - CMP导致13例患者死亡(1.0%)。在检查的可能协同因素中,发现以下因素与“明确的”ADR - CMP的发生显著相关:(a)ADR的总剂量;(b)在ADR之前和同时给予长春新碱;(c)在ADR之前给予博来霉素;(d)在ADR同时给予纵隔放疗。此外,182例接受缓慢静脉输注ADR的患者中无一例发生“明确的”ADR - CMP,而接受大剂量注射治疗的患者中有2%发生了这种情况。发现“可能的”ADR - CMP的发生与两种既往存在的病理状况(心电图[ECG]异常和高血压)显著相关,但与上述“明确的”ADR - CMP的治疗相关协同因素无关。所检查的其他变量,如性别、年龄、癌症类型、基线肝功能和环磷酰胺治疗,似乎并未影响ADR - CMP的风险。还报告了ADR治疗期间发生的ECG变化数据,发现其发生率与ECG监测频率密切相关。

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