Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo Japan.
Expert Rev Anticancer Ther. 2022 Apr;22(4):401-413. doi: 10.1080/14737140.2022.2052278. Epub 2022 Apr 4.
Curative-intent surgery is the best therapeutic option for thymic malignancies. However, patients with advanced or recurrent thymic malignancies often require palliative-intent chemotherapy or radiotherapy. Since thymic malignancies are rare cancers, the efficacy and safety of treatments have been verified based on small Phase 2 trials or retrospective studies.
We comprehensively reviewed the treatment strategies for thymic malignancies, including surgery, radiotherapy, and pharmacotherapy, including cytotoxic chemotherapy, molecular-targeted therapy, and immunotherapy. Additionally, we reviewed specific situations, such as pleural dissemination, central nervous system metastasis, and paraneoplastic syndrome.
Cytotoxic chemotherapy remains the standard option in pharmacotherapy. However, multikinase inhibitors, such as sunitinib and lenvatinib, and immune checkpoint inhibitors including pembrolizumab have been developed to treat thymic carcinomas. Now, a Phase 2 study is evaluating whether lenvatinib plus pembrolizumab benefits patients with type B3 thymoma or thymic carcinoma. Phosphatidylinositol 3-kinase/AKT/mammalian target of rapamycin inhibitors may contribute to disease control and octreotide scan is only applicable to somatostatin analogues. Although the genomic characteristics of thymic malignancies have been analyzed, few actionable mutations have been detected in general. The development of a treatment strategy using combination pharmacotherapy is anticipated.
根治性手术是治疗胸腺癌的最佳选择。然而,对于晚期或复发性胸腺癌患者,常需要姑息性化疗或放疗。由于胸腺癌是罕见的癌症,其治疗效果和安全性主要基于小样本的 2 期临床试验或回顾性研究。
我们全面回顾了胸腺癌的治疗策略,包括手术、放疗和药物治疗,包括细胞毒性化疗、分子靶向治疗和免疫治疗。此外,我们还回顾了一些特殊情况,如胸膜播散、中枢神经系统转移和副肿瘤综合征。
细胞毒性化疗仍然是药物治疗的标准选择。然而,已经开发出多激酶抑制剂,如舒尼替尼和仑伐替尼,以及免疫检查点抑制剂,如派姆单抗,用于治疗胸腺癌。目前,一项 2 期研究正在评估仑伐替尼联合派姆单抗是否有益于 B3 型胸腺瘤或胸腺癌患者。磷酸肌醇 3-激酶/AKT/哺乳动物雷帕霉素靶蛋白抑制剂可能有助于控制疾病,奥曲肽扫描仅适用于生长抑素类似物。尽管已经分析了胸腺癌的基因组特征,但一般来说,很少发现可操作的突变。预计将制定一种联合药物治疗策略。