Yap H Y, Blumenschein G R, Schell F C, Buzdar A U, Valdivieso M, Bodey G P
Ann Intern Med. 1981 Dec;95(6):694-7. doi: 10.7326/0003-4819-95-6-694.
Thirty-one patients who had metastatic breast cancer extensively pretreated with combination chemotherapy, including doxorubicin, were tested with dihydroxyanthracenedione, 3 to 4 mg/m2 body surface area daily for 5 consecutive days every 4 weeks. Of 27 evaluable patients, one achieved a complete response and five had partial responses. Furthermore, responses were seen in patients who were refractory to doxorubicin, indicating a lack of cross-resistance between doxorubicin and dihydroxyanthracenedione. Acute drug toxicity was insignificant except for severe granulocytopenia at the dose level of 4 mg/m2 . d. The median duration of remission had not been reached, but was more than 26 weeks, with four of the six responding patients still in remission at last follow-up. We believe that dihydroxyanthracenedione has significant activity against refractory metastatic breast cancer and further evaluation is warranted.
31例曾接受包括阿霉素在内的联合化疗广泛预处理的转移性乳腺癌患者,接受了二羟基蒽二酮治疗,剂量为3至4毫克/平方米体表面积,每4周连续5天每日给药。在27例可评估的患者中,1例获得完全缓解,5例部分缓解。此外,在对阿霉素耐药的患者中也观察到缓解,表明阿霉素和二羟基蒽二酮之间不存在交叉耐药性。除了在4毫克/平方米·天的剂量水平出现严重粒细胞减少外,急性药物毒性不明显。缓解期的中位数尚未达到,但超过了26周,6例有反应的患者中有4例在最后一次随访时仍处于缓解状态。我们认为二羟基蒽二酮对难治性转移性乳腺癌具有显著活性,值得进一步评估。