The Ohio State University, Columbus, OH.
Hematology Am Soc Hematol Educ Program. 2020 Dec 4;2020(1):101-106. doi: 10.1182/hematology.2020000093.
Targeting CD20 with the monoclonal antibody rituximab has improved survival in patients with aggressive B-cell lymphomas, the majority of which are cured with chemoimmunotherapy. Patients progressing through or relapsing after their treatment have a poor prognosis. Despite a number of promising novel agents with efficacy in relapsed disease, randomized trials building on the chemoimmunotherapy backbone have failed to show further survival benefit. Significant progress has been made in the last few years in relapsed or refractory disease with the emergence of therapies that harness the patient's immune system to fight disease. The approval of 2 chimeric antigen receptor T-cell products has provided potential for curative therapy, although challenges remain with toxicities and access. The approval of the antibody drug conjugate polatuzumab in combination with chemoimmunotherapy has offered survival benefit to patients who are not candidates for more aggressive approaches and has the potential to change the standard of care for initial management. Several targeted agents have proven effective, but the majority do not produce durable responses, requiring development in combination with other targeted or conventional therapies. Herein, promising targets in aggressive lymphoma with the greatest potential for improving outcomes in these patients are discussed. Novel therapies, their toxicities, and their potential role in initial or subsequent treatment are highlighted.
用单克隆抗体利妥昔单抗靶向 CD20 已经改善了侵袭性 B 细胞淋巴瘤患者的生存率,其中大多数患者通过化疗免疫治疗得到治愈。在治疗过程中进展或复发的患者预后较差。尽管有许多有前途的新型药物在复发性疾病中具有疗效,但基于化疗免疫治疗基础的随机试验未能显示出进一步的生存获益。在复发或难治性疾病方面,过去几年取得了重大进展,出现了利用患者免疫系统对抗疾病的治疗方法。两种嵌合抗原受体 T 细胞产品的批准为治愈性治疗提供了可能,尽管仍然存在毒性和可及性方面的挑战。抗体药物偶联物 polatuzumab 与化疗免疫治疗联合的批准为不适合更积极治疗方法的患者提供了生存获益,并有可能改变初始治疗的护理标准。几种靶向药物已被证明有效,但大多数药物不能产生持久的反应,需要与其他靶向或常规治疗联合开发。本文讨论了侵袭性淋巴瘤中最有希望改善这些患者预后的靶点。强调了新型疗法的毒性及其在初始或后续治疗中的潜在作用。