Ko Andrew H
Department of Medicine, University of California, San Francisco Comprehensive Cancer Center, San Francisco, CA, USA.
Semin Oncol. 2007 Aug;34(4):354-64. doi: 10.1053/j.seminoncol.2007.05.002.
Pancreatic cancer represents the fourth leading cause of cancer-related mortality in the United States. The vast majority of patients are diagnosed at advanced stages of the disease, at which time gemcitabine-based chemotherapy is typically offered as the standard of care. However, as investigators have arrived at a greater understanding of pancreatic tumor biology, newer therapeutic agents that "target" specific pathways or molecules governing the growth, spread, and maintenance of tumor cells have gained considerable interest. Erlotinib, an orally bioavailable small molecule inhibitor of the epidermal growth factor receptor, is the first of these targeted compounds to be approved for use in combination with gemcitabine for patients with advanced pancreatic cancer. Other targeted agents, including monoclonal antibodies and small molecule inhibitors aimed at a variety of targets, also have been extensively evaluated, with limited success to date. A newer strategy worth pursuing involves tailoring an individual patient's therapy according to the molecular characteristics of both host and tumor, as has shown promise in other solid tumor types.
胰腺癌是美国癌症相关死亡的第四大主要原因。绝大多数患者在疾病晚期被诊断出来,此时基于吉西他滨的化疗通常作为标准治疗方案。然而,随着研究人员对胰腺肿瘤生物学有了更深入的了解,“靶向”特定途径或控制肿瘤细胞生长、扩散和维持的分子的新型治疗药物引起了广泛关注。厄洛替尼是一种口服生物利用度高的表皮生长因子受体小分子抑制剂,是第一种被批准与吉西他滨联合用于晚期胰腺癌患者的靶向化合物。其他靶向药物,包括针对多种靶点的单克隆抗体和小分子抑制剂,也已得到广泛评估,但迄今为止成效有限。一种值得探索的新策略是根据宿主和肿瘤的分子特征为个体患者量身定制治疗方案,这在其他实体瘤类型中已显示出前景。