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非霍奇金淋巴瘤的治疗

Therapy of non-Hodgkin's lymphoma.

作者信息

Coffey J, Hodgson D C, Gospodarowicz M K

机构信息

Department of Radiation Oncology, Princess Margaret Hospital, Toronto, Ontario, Canada.

出版信息

Eur J Nucl Med Mol Imaging. 2003 Jun;30 Suppl 1:S28-36. doi: 10.1007/s00259-003-1157-6. Epub 2003 Apr 12.

Abstract

Non-Hodgkin's lymphomas are a heterogeneous group of malignancies of the lymphoid system. The exact etiology for most lymphomas has not been determined, but both viral and bacterial infections have been shown to be important etiologic factors. The WHO classification of hematopoietic and lymphoid tumours classifies lymphomas into B-cell and T-cell neoplasms. B-cell lymphomas account for more than 85% of all lymphomas. The Ann Arbor staging classification has been adopted by the AJCC and UICC as a standard for classifying extent of anatomic disease. The two most common histologic disease entities are follicular lymphomas and diffuse large B-cell lymphomas. The management of follicular lymphomas is used as a paradigm for the management of all indolent lymphomas. Radiation therapy is used for stage I and II disease, while alkylating agent chemotherapy, immunotherapy and radioimmunotherapy are most frequently used in stage III and IV disease that requires treatment. Most patients with follicular lymphoma enjoy prolonged survival, but at present there is no evidence that those with stage III and IV follicular lymphoma can be cured. Diffuse large B-cell lymphomas serve as a paradigm for treating aggressive lymphomas. Stage I and II diffuse large cell lymphomas are generally treated with combined modality therapy with doxorubicin-based chemotherapy followed by involved field radiation therapy, while those with stage III and IV disease are treated with chemotherapy alone. Patients who fail initial management are treated with further chemotherapy. High-dose chemotherapy with stem cell rescue has been shown to be particularly effective as salvage treatment for diffuse large cell lymphomas. The management of a heterogeneous group of primary extranodal lymphomas in general follows the above treatment principles, with additional treatment being required for those with a high risk of CNS failures, or involvement of contralateral paired organs. The management of MALT lymphomas, especially gastric MALT lymphoma, deserves special attention because of the high response rate to Helicobacter pylori eradication therapy.

摘要

非霍奇金淋巴瘤是淋巴系统的一组异质性恶性肿瘤。大多数淋巴瘤的确切病因尚未确定,但病毒和细菌感染已被证明是重要的病因因素。世界卫生组织造血与淋巴组织肿瘤分类将淋巴瘤分为B细胞和T细胞肿瘤。B细胞淋巴瘤占所有淋巴瘤的85%以上。美国癌症联合委员会(AJCC)和国际抗癌联盟(UICC)采用Ann Arbor分期分类作为解剖学疾病范围分类的标准。两种最常见的组织学疾病实体是滤泡性淋巴瘤和弥漫性大B细胞淋巴瘤。滤泡性淋巴瘤的治疗被用作所有惰性淋巴瘤治疗的范例。放射治疗用于I期和II期疾病,而烷化剂化疗、免疫治疗和放射免疫治疗最常用于需要治疗的III期和IV期疾病。大多数滤泡性淋巴瘤患者生存期延长,但目前没有证据表明III期和IV期滤泡性淋巴瘤患者可以治愈。弥漫性大B细胞淋巴瘤是侵袭性淋巴瘤治疗的范例。I期和II期弥漫性大细胞淋巴瘤一般采用以阿霉素为基础的联合化疗,随后进行受累野放射治疗,而III期和IV期疾病患者则单独接受化疗。初始治疗失败的患者接受进一步化疗。大剂量化疗联合干细胞救援已被证明作为弥漫性大细胞淋巴瘤的挽救治疗特别有效。一组异质性原发性结外淋巴瘤的治疗一般遵循上述治疗原则,对于有中枢神经系统衰竭高风险或对侧配对器官受累的患者需要额外治疗。黏膜相关淋巴组织淋巴瘤的治疗,尤其是胃黏膜相关淋巴组织淋巴瘤,因其对幽门螺杆菌根除治疗的高反应率而值得特别关注。

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