Robustelli Della Cuna G, Pavesi L, Preti P, Ganzina F
Invest New Drugs. 1983;1(4):349-53. doi: 10.1007/BF00177421.
A Phase II clinical evaluation of 4'-epi-doxorubicin has been carried out in 100 patients with various types of solid tumors. Hematopoietic toxicity was dose-limiting but reversible and of mild to moderate degree. Other acute toxic manifestations such as vomiting and alopecia were qualitatively similar to those usually reported for doxorubicin, but lower in frequency and less severe. A number of responding patients received cumulative doses of 4'-epi-doxorubicin in excess of 500 mg/m2. One patient manifested reversible clinical congestive heart failure at cumulative dose of 1,080 mg/m2. Therapeutic activity has been observed in breast carcinoma, in rectal carcinoma and in melanoma. In chemoresistant tumors as rectal cancer and melanoma 4'-epi-doxorubicin deserves further study.
已对100例患有各种实体瘤的患者进行了4'-表阿霉素的II期临床评估。造血毒性是剂量限制性的,但具有可逆性,且程度为轻度至中度。其他急性毒性表现,如呕吐和脱发,在性质上与通常报道的阿霉素相似,但频率较低且严重程度较轻。一些有反应的患者接受的4'-表阿霉素累积剂量超过500mg/m²。1例患者在累积剂量达1080mg/m²时出现可逆性临床充血性心力衰竭。在乳腺癌、直肠癌和黑色素瘤中观察到了治疗活性。在化疗耐药肿瘤如直肠癌和黑色素瘤中,4'-表阿霉素值得进一步研究。