Slovin S F, Ragupathi G, Adluri S, Ungers G, Terry K, Kim S, Spassova M, Bornmann W G, Fazzari M, Dantis L, Olkiewicz K, Lloyd K O, Livingston P O, Danishefsky S J, Scher H I
Division of Genitourinary Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, Sloan-Kettering Institute, 1275 York Avenue, New York, NY 10021, USA.
Proc Natl Acad Sci U S A. 1999 May 11;96(10):5710-5. doi: 10.1073/pnas.96.10.5710.
The complex carbohydrate molecule globo H hexasaccharide has been synthesized, conjugated to keyhole limpet hemocyanin, and administered with the immunologic adjuvant QS-21 as a vaccine for patients with prostate cancer who have relapsed after primary therapies such as radiation or surgery. Globo H is one of several candidate antigens present on prostate cancer cells that can serve as targets for immune recognition and treatment strategies. The vaccine, given as five subcutaneous vaccinations over 26 weeks, has been shown to be safe and capable of inducing specific high-titer IgM antibodies against globo H. Its immunogenicity was confirmed in prostate cancer patients with a broad range of stages and tumor burdens. Observations of several patients who had evidence of disease relapse restricted to a rising biochemical marker, prostate-specific antigen (PSA), indicated that a treatment effect could occur within 3 months after completion of the vaccine therapy. This effect was manifested as a decline of the slope of the log of PSA concentration vs. time plot after treatment compared with values before treatment. Five patients continue to have stable PSA slope profiles in the absence of any radiographic evidence of disease for more than 2 years. The concept of using PSA slope profiles in assessing early treatment effects in biological therapies such as vaccines awaits further validation in phase II and III trials. The use of a variety of lesser known candidate glycoprotein and carbohydrate antigens in prostate cancer serves as a focus for the development of a multivalent vaccine of the treatment of relapsed prostate cancer in patients with minimal tumor burden.
复合碳水化合物分子球H六糖已被合成,与钥孔戚血蓝蛋白偶联,并与免疫佐剂QS-21一起作为疫苗用于接受过放疗或手术等初始治疗后复发的前列腺癌患者。球H是前列腺癌细胞上存在的几种候选抗原之一,可作为免疫识别和治疗策略的靶点。这种疫苗在26周内进行了5次皮下接种,已证明是安全的,并且能够诱导针对球H的特异性高滴度IgM抗体。其免疫原性在广泛分期和肿瘤负荷的前列腺癌患者中得到了证实。对几名疾病复发证据仅限于生化标志物前列腺特异性抗原(PSA)升高的患者的观察表明,在疫苗治疗完成后3个月内可能会出现治疗效果。这种效果表现为治疗后PSA浓度对数与时间曲线的斜率与治疗前的值相比有所下降。5名患者在超过2年的时间里没有任何疾病的影像学证据,PSA斜率曲线持续稳定。在生物疗法如疫苗中使用PSA斜率曲线评估早期治疗效果的概念有待在II期和III期试验中进一步验证。在肿瘤负荷最小的复发前列腺癌患者中,使用多种鲜为人知的候选糖蛋白和碳水化合物抗原作为开发多价疫苗治疗复发前列腺癌的重点。