癌症食管癌的靶向治疗

S. Hassan, Victoria Makuru, U. Holzen
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引用次数: 3

摘要

食管癌包括两种不同的组织学类型,食管鳞状细胞癌(ESCC)和食管腺癌(EAC)。食管癌在预后和死亡率方面是一种严重的恶性肿瘤。ESCC仍然是世界范围内食管癌的主要组织学类型,约占世界范围内所有病例的90%。然而,EAC现在在美国和西方世界更为常见,并且是那里增长最快的癌症之一。尽管在多模式治疗选择方面取得了重大进展,但总体预后仍然很差,所有患者的5年生存率仍然低于20%。虽然食管癌最初对全身治疗反应良好,但大多数患者会复发并最终死于疾病。因此,迫切需要新的治疗方案。传统的全身治疗与新的生物制剂和/或靶向药物的结合是这些新的治疗选择之一。其中一些药物已经获得批准,而其他药物目前正在进行临床试验。这些靶向疗法已经成为治疗包括食管癌在内的许多不同类型癌症的重要工具。在此,我们回顾了食管癌靶向治疗的最新文献和正在进行的临床试验,并讨论了不同的靶向途径。目前,大多数食管癌患者仍采用紫杉醇(紫杉醇、多西紫杉醇)、铂(卡铂、顺铂)、蒽环类药物(阿霉素、表柔比星)或嘧啶类似物(5-氟尿嘧啶)等化疗药物联合治疗。未来的治疗策略应基于每个患者个体肿瘤的分子特征,并应包括量身定制的生物制剂/靶向药物
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted therapy in esophageal cancer
Esophageal cancer consists of two distinct histological types, esophageal squamous cell-carcinoma (ESCC) and esophageal adenocarcinoma (EAC). Esophageal carcinoma is a grave malignancy with regards to prognosis and mortality. ESCC remains the dominant histological type of esophageal cancer worldwide, with about 90 percent of all cases worldwide. However, EAC is now much more common in the United States and the Western World, and represents one of the fastest growing cancers there. Despite significant progress in multimodality treatment options, the overall prognosis remains poor, and 5-year survival rates for all-comers are still below 20 percent. Although esophageal cancer initially responds well to systemic therapy, most patients recur and eventually die from their disease. Therefore, new treatment options are urgently needed. The combination of traditional systemic therapy with new biologicals and/or targeted agents is one of these new treatment options. Some of these agents are already approved, while others are currently undergoing clinical trials. These targeted therapies have emerged as an important tool for the treatment of many different cancer types, including esophageal cancer. Herein, we review the recent literature and ongoing clinical trials in esophageal cancer targeted therapies, and discuss the different targeted pathways. Currently, most esophageal cancer patients are still treated with a combination of chemotherapies like taxanes (paclitaxel, docetaxel), platinums (carboplatin, cisplatin), anthracyclines (doxorubicin, epirubicin) or pyrimidine analogs (5-fluorouracil). Future treatment strategies should be based on the molecular features of each patient’s individual tumor, and should include biologicals/targeted agents tailored to these
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