Chang A Y, Fisher H A, Spiers A S, Boros L
J Interferon Res. 1986 Dec;6(6):713-5. doi: 10.1089/jir.1986.6.713.
Nine patients with hormone-resistant prostate carcinoma were treated with subcutaneous injection of recombinant human interferon-alpha 2 (rHuIFN-alpha 2), 5-10 X 10(6) U/m2, three times a week. One patient had a mixed clinical response with reduction of bone pain. The study was closed due to intolerable grade III and IV toxicities including weight loss (8/9), fatigue/malaise (7/9), central nervous system toxicity (4/9), leukopenia (3/9), and uncontrollable nausea and vomiting (2/9). These toxicities resulted in deterioration of performance status. It is concluded that rHuIFN-alpha 2, at least at the dose and schedule studied, should not be used for the treatment of patients with hormone-resistant prostate carcinoma.
9例激素抵抗性前列腺癌患者接受重组人干扰素α2(rHuIFN-α2)皮下注射治疗,剂量为5-10×10⁶U/m²,每周3次。1例患者有混合临床反应,骨痛减轻。该研究因无法耐受的Ⅲ级和Ⅳ级毒性反应而终止,这些毒性反应包括体重减轻(8/9)、疲劳/不适(7/9)、中枢神经系统毒性(4/9)、白细胞减少(3/9)以及无法控制的恶心和呕吐(2/9)。这些毒性反应导致患者身体状况恶化。结论是,至少在所研究的剂量和给药方案下,rHuIFN-α2不应被用于治疗激素抵抗性前列腺癌患者。