Brockstein B, Samuels B, Humerickhouse R, Arietta R, Fishkin P, Wade J, Sosman J, Vokes E E
University of Chicago Hospitals, Section of Hematology/Oncology, IL, USA.
Invest New Drugs. 2001;19(3):249-54. doi: 10.1023/a:1010628903248.
Bryostatin 1 is a marine derived macrolactone with antineoplastic activity modulated through protein kinase C, and with good activity in in vitro and in vivo models. There are few drugs that offer palliation for metastatic soft-tissue sarcoma and head and neck cancer, and drugs with new mechanisms of action warrant detailed disease specific study.
Two phase II studies for patients with incurable soft tissue sarcoma (12), or head and neck cancer (12) were conducted. Patients were treated with bryostatin, 120 mg/m2/72 hours every 2 weeks for 3 cycles prior to re-evaluation. Most patients had received prior chemotherapy.
No patients had objective responses to therapy. Six patients had brief periods of disease stabilization. Toxicity was generally mild, with myalgia being prominent (n=8). Hyponatremia, not previously described, occurred in 5 patients. The mechanism of this toxicity was unclear.
Bryosytatin 1 given as a single agent for advanced adult soft tissue sarcoma and head and neck cancer is inactive. Myalgia and hyponatremia were the predominant toxicities.
苔藓抑素1是一种源自海洋的大环内酯类化合物,具有通过蛋白激酶C调节的抗肿瘤活性,并且在体外和体内模型中具有良好的活性。对于转移性软组织肉瘤和头颈癌,几乎没有药物能够提供姑息治疗,具有新作用机制的药物值得进行详细的疾病特异性研究。
针对无法治愈的软组织肉瘤患者(12例)或头颈癌患者(12例)开展了两项II期研究。患者接受苔藓抑素治疗,每2周一次,剂量为120mg/m²/72小时,共3个周期,之后进行重新评估。大多数患者之前接受过化疗。
没有患者对治疗产生客观反应。6例患者病情有短暂稳定期。毒性一般较轻,以肌痛最为突出(n = 8)。5例患者出现了之前未描述过的低钠血症。这种毒性的机制尚不清楚。
单独使用苔藓抑素1治疗晚期成人软组织肉瘤和头颈癌没有活性。肌痛和低钠血症是主要的毒性反应。