Ansell Stephen M
Division of Hematology, Mayo Clinic, Rochester, MN.
Mayo Clin Proc. 2015 Nov;90(11):1574-83. doi: 10.1016/j.mayocp.2015.07.005.
Hodgkin lymphoma is a rare B-cell malignant neoplasm affecting approximately 9000 new patients annually. This disease represents approximately 11% of all lymphomas seen in the United States and comprises 2 discrete disease entities--classical Hodgkin lymphoma and nodular lymphocyte-predominant Hodgkin lymphoma. Within the subcategorization of classical Hodgkin lymphoma are defined subgroups: nodular sclerosis, mixed cellularity, lymphocyte depletion, and lymphocyte-rich Hodgkin lymphoma. Staging of this disease is essential for the choice of optimal therapy. Prognostic models to identify patients at high or low risk for recurrence have been developed, and these models, along with positron emission tomography, are used to provide optimal therapy. The initial treatment for patients with Hodgkin lymphoma is based on the histologic characteristics of the disease, the stage at presentation, and the presence or absence of prognostic factors associated with poor outcome. Patients with early-stage Hodgkin lymphoma commonly receive combined-modality therapies that include abbreviated courses of chemotherapy followed by involved-field radiation treatment. In contrast, patients with advanced-stage Hodgkin lymphoma commonly receive a more prolonged course of combination chemotherapy, with radiation therapy used only in selected cases. For patients with relapse or refractory disease, salvage chemotherapy followed by high-dose treatment and an autologous stem cell transplant is the standard of care. For patients who are ineligible for this therapy or those in whom high-dose therapy and autologous stem cell transplant have failed, treatment with brentuximab vedotin is a standard approach. Additional options include palliative chemotherapy, immune checkpoint inhibitors, nonmyeloablative allogeneic stem cell transplant, or participation in a clinical trial testing novel agents.
霍奇金淋巴瘤是一种罕见的B细胞恶性肿瘤,每年约有9000名新患者。这种疾病约占美国所有淋巴瘤的11%,包括2种不同的疾病实体——经典型霍奇金淋巴瘤和结节性淋巴细胞为主型霍奇金淋巴瘤。在经典型霍奇金淋巴瘤的亚分类中有明确的亚组:结节硬化型、混合细胞型、淋巴细胞消减型和富于淋巴细胞型霍奇金淋巴瘤。该疾病的分期对于选择最佳治疗至关重要。已经开发出用于识别复发风险高或低的患者的预后模型,这些模型与正电子发射断层扫描一起用于提供最佳治疗。霍奇金淋巴瘤患者的初始治疗基于疾病的组织学特征、就诊时的分期以及与不良预后相关的预后因素的存在与否。早期霍奇金淋巴瘤患者通常接受综合治疗,包括短期化疗疗程,随后进行受累野放射治疗。相比之下,晚期霍奇金淋巴瘤患者通常接受更长疗程的联合化疗,仅在特定情况下使用放射治疗。对于复发或难治性疾病患者,挽救性化疗后进行大剂量治疗和自体干细胞移植是标准治疗方法。对于不符合这种治疗条件或大剂量治疗和自体干细胞移植失败的患者,使用维布妥昔单抗治疗是一种标准方法。其他选择包括姑息性化疗、免疫检查点抑制剂、非清髓性异基因干细胞移植或参与测试新型药物的临床试验。