Zalupski M M, Benedetti J, Balcerzak S P, Hutchins L F, Belt R J, Hantel A, Goodwin J W
Wayne State University Medical Center, Detroit, MI.
Invest New Drugs. 1993 Nov;11(4):337-41. doi: 10.1007/BF00874435.
Piroxantrone is an anthrapyrazole compound undergoing phase II testing in a variety of diseases. The anthrapyrazoles are a series of compounds synthesized with the intent of maintaining the broad antitumor activity of anthracyclines, but with lessened cardiac toxicity. The Southwest Oncology Group (SWOG) conducted a phase II trial of piroxantrone in advanced soft tissue sarcoma. Treatment consisted of piroxantrone 150 mg/M2 administered intravenously over 1 hour every 21 days. Twenty-five eligible patients were registered to the trial. Twenty-three patients received treatment and are fully evaluable for response and toxicity. Two partial responses were seen for an overall response rate of 9% (95% confidence limit 1%-28%). Abnormal cardiac ejection fraction occurred in five patients, and fatal congestive heart failure developed in one patient on study. Toxicities other than cardiac were tolerable. Based on the observed response rate and cardiac toxicity, further trials of piroxantrone in the treatment of soft tissue sarcoma do not appear warranted.
吡罗蒽醌是一种正在多种疾病中进行II期试验的蒽吡唑化合物。蒽吡唑类是一系列合成化合物,旨在保持蒽环类药物的广泛抗肿瘤活性,但心脏毒性降低。西南肿瘤协作组(SWOG)开展了一项吡罗蒽醌治疗晚期软组织肉瘤的II期试验。治疗方案为每21天静脉输注吡罗蒽醌150mg/M²,持续1小时。25名符合条件的患者登记参加该试验。23名患者接受了治疗,可对反应和毒性进行全面评估。观察到2例部分缓解,总缓解率为9%(95%置信区间1%-28%)。5例患者出现心脏射血分数异常,1例研究中的患者发生致命性充血性心力衰竭。除心脏毒性外的其他毒性均可耐受。基于观察到的缓解率和心脏毒性,吡罗蒽醌进一步用于治疗软组织肉瘤的试验似乎没有必要。