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淋巴瘤疫苗治疗:阳性、对照 III 期临床试验后的下一步。

Lymphoma vaccine therapy: next steps after a positive, controlled phase III clinical trial.

机构信息

Department of Lymphoma & Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Semin Oncol. 2012 Jun;39(3):253-62. doi: 10.1053/j.seminoncol.2012.02.014.

Abstract

Many of the efforts toward developing vaccines against human malignancies have been frustrated by the lack of identification of a tumor-specific antigen that would allow tumor cells to be distinguished from normal cells. Idiotypic determinants of the surface immunoglobulin (Ig) associated with a given patient's B-cell lymphoma are unique to that tumor, and can thus serve as a tumor-specific marker. When conjugated to the immune carrier keyhole limpet hemocyanin (KLH), vaccination with an idiotype protein vaccine has been able to improve length of freedom from disease relapse in patients with follicular lymphoma (FL) in a minimal residual disease (MRD) state after induction therapy, as demonstrated in a recent randomized, controlled phase III trial. In addition to predictive biomarker discovery, using residual autologous tumor and blood samples from patients vaccinated on the phase III trial, we have now developed a next generation idiotype DNA vaccine with the goal of reducing vaccine production time while maintaining efficacy. A first-in-human study is planned to evaluate its use in patients with asymptomatic phase lymphoplasmacytic lymphoma.

摘要

许多针对人类恶性肿瘤开发疫苗的努力都因缺乏能够区分肿瘤细胞和正常细胞的肿瘤特异性抗原而受挫。与特定患者的 B 细胞淋巴瘤相关的表面免疫球蛋白(Ig)的独特型决定簇是该肿瘤所特有的,因此可以作为肿瘤特异性标志物。当与免疫载体血蓝蛋白(KLH)偶联时,用独特型蛋白疫苗进行疫苗接种已能够改善诱导治疗后处于微小残留疾病(MRD)状态的滤泡性淋巴瘤(FL)患者的无疾病复发时间,这在最近的一项随机、对照的 III 期试验中得到了证明。除了预测性生物标志物的发现,利用 III 期试验中接种疫苗的患者的残留自体肿瘤和血液样本,我们现在已经开发了一种下一代独特型 DNA 疫苗,目标是在保持疗效的同时减少疫苗生产时间。计划进行首例人体研究,以评估其在无症状期淋巴浆细胞淋巴瘤患者中的应用。

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