摘要
几十年来,可用抗癌疗法大多基于非特异性细胞毒性疗法。这些细胞生长抑制剂的组合对一些患者亚群有效,但经常被广泛的毒性和/或肿瘤抗性的发展所限制。虽然标准化疗方案仍停留在与癌症斗争的一个共同的治疗手段,免疫日益革新一些恶性血液病的治疗策略。对于患B细胞淋巴增生性疾病的患者子集,引入随后开发的几类抗CD20单克隆抗体(mAbs)已经改进了总的反应率,并在一定程度上提高了患者的整体存活率。利妥昔单抗,最彻底探索嵌合小鼠抗人源化抗CD20单克隆抗体,已被广泛地并成功地引入到肿瘤血液学中,也引入到了其他医药领域,例如transfusiology或风湿病。目前,几个新一代的抗CD20单克隆抗体正处于临床前和临床研究评估的不同阶段,以进一步提高疗效和克服阻力机制。利妥昔单抗,最彻底探索嵌合小鼠抗人类抗CD20单克隆抗体,已被广泛地并成功地引入到肿瘤血液学中,也引入到了其他医药领域,例如transfusiology或风湿病。目前,几个新一代的抗CD20单克隆抗体正处于临床前和临床研究评估的不同阶段,以进一步提高疗效和克服阻力机制。对不同类别的抗CD20单克隆抗体的抗癌特性的直接机制性质尚未完全清楚。这反映在新的抗CD20药物调查期间不同的方法。迄今,三种类型的抗CD20单克隆抗体的已被阐述。在此文中,我们侧重于对B细胞淋巴组织的恶性肿瘤CD20抗原靶向疗法既包括目前可用的疗法也包括临床前或临床研究。
关键词: 抗CD20单克隆抗体利妥昔单抗;obinutuzumab;奥法木单抗;单克隆抗体;淋巴组织肿瘤;免疫化疗;单克隆抗体;B细胞淋巴恶性肿瘤
图形摘要
Current Drug Targets
Title:Development of Anti-CD20 Antigen-Targeting Therapies for B-cell Lymphoproliferative Malignancies - The State of the Art
Volume: 17 Issue: 9
Author(s): Magdalena Witkowska, Piotr Smolewski
Affiliation:
关键词: 抗CD20单克隆抗体利妥昔单抗;obinutuzumab;奥法木单抗;单克隆抗体;淋巴组织肿瘤;免疫化疗;单克隆抗体;B细胞淋巴恶性肿瘤
摘要: For decades, the available anticancer therapies were mostly based on nonspecific cytotoxic regimens. These cytostatic combinations, while effective in some subpopulations of patients, are often limited by extensive toxicity and/or development of tumor resistance. Although standard chemotherapy still remains a common therapeutic tool in the fight with cancer, immunotherapy increasingly revolutionizes treatment strategy for several hematologic malignancies. For a subset of patients with B-cell lymphoproliferative disease, the introduction of subsequently developed classes of anti-CD20 monoclonal antibodies (mAbs) has resulted in improved overall response rates and, to some extent, patient overall survival. Rituximab, the most thoroughly-explored chimeric mouse anti-human anti-CD20 mAb, has been widely and successfully introduced to oncohematology, but also to other fields of medicine, such as transfusiology or rheumatology. Currently, several new generation anti-CD20 mAbs are undergoing different stages of preclinical and clinical studies of assessment to further improve the outcome and overcome mechanisms of resistance. The nature of the direct mechanisms responsible for the anticancer properties of different classes of anti-CD20 mAbs is still not fully understood. This is reflected in different approaches during the investigation of novel anti-CD20 agents. So far, three classes of anti- CD20 mAb have been described. In this review, we focus on CD20 antigen-targeting therapies both currently available and undergoing preclinical or clinical investigation for B-cell lymphoproliferative malignancies.
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Cite this article as:
Magdalena Witkowska, Piotr Smolewski , Development of Anti-CD20 Antigen-Targeting Therapies for B-cell Lymphoproliferative Malignancies - The State of the Art, Current Drug Targets 2016; 17 (9) . https://dx.doi.org/10.2174/1389450116666150907105306
DOI https://dx.doi.org/10.2174/1389450116666150907105306 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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